Comorbid anxiety-like behavior in a rat model of colitis is mediated by an upregulation of corticolimbic fatty acid amide hydrolase

Haley A Vecchiarelli; Maria Morena; Catherine M Keenan; Vincent Chiang; Kaitlyn Tan; Min Qiao; Kira Leitl; Alessia Santori; Quentin J Pittman; Keith A Sharkey; Matthew N Hill

doi:10.1038/s41386-020-00939-7

. 2021 Jan 15;46(5):992–1003. doi: 10.1038/s41386-020-00939-7

Comorbid anxiety-like behavior in a rat model of colitis is mediated by an upregulation of corticolimbic fatty acid amide hydrolase

Haley A Vecchiarelli ^1,^2,^3,^✉, Maria Morena ^2,^3,^4,⁵, Catherine M Keenan ^2,^6,⁷, Vincent Chiang ^2,^3,^4,⁵, Kaitlyn Tan ^2,^3,^4,⁵, Min Qiao ^2,^3,^4,⁵, Kira Leitl ^2,^3,^4,⁵, Alessia Santori ^2,^3,^4,⁵, Quentin J Pittman ^2,^3,^6,⁷, Keith A Sharkey ^2,^6,⁷, Matthew N Hill ^2,^3,^4,^5,^✉

PMCID: PMC8115350 PMID: 33452437

Abstract

Peripheral inflammatory conditions, including those localized to the gastrointestinal tract, are highly comorbid with psychiatric disorders such as anxiety and depression. These behavioral symptoms are poorly managed by conventional treatments for inflammatory diseases and contribute to quality of life impairments. Peripheral inflammation is associated with sustained elevations in circulating glucocorticoid hormones, which can modulate central processes, including those involved in the regulation of emotional behavior. The endocannabinoid (eCB) system is exquisitely sensitive to these hormonal changes and is a significant regulator of emotional behavior. The impact of peripheral inflammation on central eCB function, and whether this is related to the development of these behavioral comorbidities remains to be determined. To examine this, we employed the trinitrobenzene sulfonic acid-induced model of colonic inflammation (colitis) in adult, male, Sprague Dawley rats to produce sustained peripheral inflammation. Colitis produced increases in behavioral measures of anxiety and elevations in circulating corticosterone. These alterations were accompanied by elevated hydrolytic activity of the enzyme fatty acid amide hydrolase (FAAH), which hydrolyzes the eCB anandamide (AEA), throughout multiple corticolimbic brain regions. This elevation of FAAH activity was associated with broad reductions in the content of AEA, whose decline was driven by central corticotropin releasing factor type 1 receptor signaling. Colitis-induced anxiety was reversed following acute central inhibition of FAAH, suggesting that the reductions in AEA produced by colitis contributed to the generation of anxiety. These data provide a novel perspective for the pharmacological management of psychiatric comorbidities of chronic inflammatory conditions through modulation of eCB signaling.

Subject terms: Experimental organisms, Stress and resilience, Limbic system, Behavioural methods, Anxiety

Introduction

In peripheral inflammatory conditions, such as inflammatory bowel diseases (IBD), comorbid anxiety and depression are associated with increased disease activity, greater rate of relapse and reduced responsiveness to therapies [1–5], significantly reducing patient quality of life [6, 7]. It is established in cohorts from around the world that patients with IBD (ulcerative colitis and Crohn’s disease; combined, and each, separately,) show a 2–3 times greater incidence of anxiety and depression [2–4, 8–29]. It is likely that the driving force behind these psychiatric comorbidities is disease activity [8, 13, 30–35], implying, at least partially, that inflammation and a dysregulation of the gut-brain axis may be involved in the pathogenesis of psychiatric comorbidities in IBD. Both basally and during disease states, the gut-brain axis allows for bidirectional communication between the brain and the gut, including at the levels of the autonomic nervous system and circumventricular organs [36]. As such, understanding the neural mechanisms that underlie the generation of anxiety and depression in peripheral inflammatory disorders may allow for the development of novel treatment approaches to manage these comorbid symptoms that severely impact individuals with these disorders.

Peripheral inflammation, particularly within the gut, is known to be a potent activator of the hypothalamic-pituitary-adrenal (HPA) axis [37, 38]. Sustained elevations in circulating glucocorticoid hormones can modulate central processes, including those involved in the regulation of emotional behavior [39, 40]. One system known to be sensitive to hormonal components of the HPA axis, and that is a significant regulator of emotional behavior, is the endocannabinoid (eCB) system [41–43].

Constitutive eCB signaling constrains anxiety, as acute pharmacological disruption of eCB function rapidly produces a state of anxiety [44–46]. Similarly, exposure to stress is known to increase activity of the enzyme fatty acid amide hydrolase (FAAH), which metabolizes the eCB ligand anandamide (AEA) [47–49], through the release of the neuropeptide corticotropin-releasing factor (CRF; alternatively corticotropin-releasing hormone (CRH)) and subsequent activation of the CRF type 1 receptor (CRF-R1) [50]. This suppression of AEA signaling by CRF-R1 activity promotes the development of anxiety, largely through coordinated actions in corticolimbic circuits encompassing the amygdala [50], medial prefrontal cortex [51], and hippocampus [52]. Interestingly, CRF signaling is also known to be important for the development of anxiety in response to inflammation, as blockade of CRF signaling can dampen anxiety and other adverse behavioral responses to a variety of experimental inflammatory conditions such as cerebral ischemia [53], arthritis [54, 55], and inflammatory pain [54, 56, 57]. As sustained inflammation is known to produce an upregulation of central CRF [57–59], it seems plausible that this could result in a suppression of AEA signaling that in turn could contribute to the development of comorbid anxiety in colitis.

To further examine the relationship between eCBs and peripheral inflammation, we utilized a rat model of colitis to investigate the potential role that the eCB system plays in the mechanisms underlying psychiatric comorbidity in chronic inflammatory diseases. Colitis represents an ideal condition for this investigation, as humans afflicted with colitis exhibit considerable psychiatric comorbidities, particularly anxiety [1–5], and antagonism of CRF-R1 in humans with IBD has been found to normalize both alterations in neural connectivity and changes in emotional behavior [60, 61]. Rodent models of colitis produce a sustained state of systemic inflammation [62–65], exhibit upregulation of central CRF [66–69] and recapitulate the anxiety phenotype [70–73] seen in the human condition, making them an ideal model to explore the role of eCBs in these processes.

Methods and materials

Animals

All experiments utilized adult (~300–350 g at time of colitis induction), male or female, Sprague Dawley rats from Charles River (Saint Constant, QC, Canada, RGD Cat# 734476; RRID:RGD_734476). Animals were allowed to acclimate for at least one week prior to experiment onset. Rats were paired-housed under specified pathogen free conditions on a 12:12 h light/dark cycle with ad libitum access to food and water. All experiments were conducted during the light phase of the cycle. All animal protocols were approved by the University of Calgary Animal Care Committee and followed guidelines from the Canadian Council for Animal Care. For each set of experiments described below, animals from a minimum of 2, and up to 4, cohorts were used, aside from locomotor activity which was assessed in a single cohort.

Colitis induction and assessment

Under brief isoflurane anesthesia, rats received an intracolonic bolus of 2,4,6-trinitrobenzenesulfonic acid (TNBS) (Millipore Sigma, Darmstadt, Germany, #92822; 0.45 mL, 50 mg/mL, 50% [vol/vol] in ethanol/water), via a cannula, inserted 7 cm proximal to the anus [74–77]. TNBS haptenizes self and microbial proteins, which makes them available to initiate an immune response in the host’s own immune system [78–80]. Control animals received the same volume of saline delivered similarly, as is standard in the field. Body weight was monitored. Behavioral testing took place 1-week after the induction of colitis after which rats were euthanized by decapitation. Colons were quickly removed, rinsed with ice-cold physiological saline (0.9%) and cut open longitudinally to enable macroscopic scoring for damage and inflammation, including adhesions, diarrhea and degree of ulceration. This score was adapted from those previously reported [74, 77] and is described in the Supplementary Materials. An ~100 mg sample of colon was excised, snap frozen and stored at −80 °C until assayed for myeloperoxidase (MPO) activity, as previously described [74–77] and in the Supplementary Materials.

Behavioral measures

Locomotor activity

Ambulatory activity was assessed using the Opto-Varimex-5 Auto Track (Columbus Instruments, Columbus, OH, USA) infrared beam activity monitor with a 17.5”x17.5” arena as previously described [81]. Day 0 testing occurred prior to TNBS or saline administration. Data were normalized within an animal to a percentage of its Day 0 activity.

Elevated plus maze (EPM)

Animals were subjected to handling and body weight measurement in the behavior testing room at least 5 days prior to anxiety testing. EPM (Med Associates, Fairfax, VT, USA) testing occurred on Day 7 following colitis induction under dim light and with a white noise background. EPM was performed for 5 min as previously described [82] and is detailed in the Supplementary Materials.

Biochemical and molecular measures

Corticosterone enzyme-linked immunosorbent assay (ELISA)

After behavioral experiments were completed on Day 7 after the induction of colitis, trunk blood was collected as previously described [83, 84] and plasma corticosterone levels were assayed using a commercially available ELISA kit (Cayman Chemical Company, Ann Arbor, Michigan, USA, #500655), according to the manufacturer’s protocol.

Endocannabinoid measurements

Excisions of brain structures were performed on ice as described previously [85] and samples were immediately snap frozen and stored at −80 °C. Analysis of AEA, and the other primary eCB 2-arachidonoylglycerol (2-AG), was conducted through liquid chromatography/tandem mass spectrometry on an Eksigent ekspert micro liquid chromatographer 200 coupled to an AB Sciex Qtrap 5500 mass spectrometer (SCIEX, Framingham, MA, USA) as previously described [82, 86] and in the Supplementary Materials.

Enzyme activity assays

Brain structures were excised on ice [85] and samples were then immediately snap frozen and stored at −80 °C. Brain tissues were homogenized and membrane fractions were isolated as described previously [50].

The activity of the enzyme FAAH, which is responsible for the degradation of AEA, was measured as the conversion of [³H]-AEA to [³H]-ethanolamine [87]. Similarly, monoacylglycerol lipase (MAGL) activity was measured as the conversion of [³H]-2-oleoylglycerol (2-OG) to [³H]-glycerol [88]. The maximal hydrolytic activity (V_max) of FAAH and MAGL and the binding affinities (K_m) of AEA for FAAH and 2-AG for MAGL were determined by fitting the data to the Michaelis-Menten equation using Prism v8 (GraphPad, San Diego, CA, USA, RRID:SCR_002798).

Gene expression analysis

mRNA isolation and cDNA synthesis was performed as previously described [50, 83, 84] and detailed in the Supplemental Materials, using magnetic bead homogenization with a TissueLyser LT (Qiagen, Hilden, Germany) and the RNeasy Plus Universal Mini Kit (Qiagen, #73404) on a Qiacube (Qiagen, RRID:SCR_018618) followed by the QuantiTect Reverse Transcription Kit (Qiagen, #205314) according to the manufacturer’s protocols. Primers for genes of interest were designed using IDTDNA PrimerQuest (Coralville, Iowa, USA) and acquired from IDTDNA (Table S1). qPCR was performed as previously described (1 min at 90 °C, 40 cycles of 95 °C for 5 s and 60 °C for 30 s, before a final melt step) using PerfeCTa SYBR Green Fast Mix (QuantaBio, Beverly, MA, USA, #95072) on a RotoGene Q light cycler (Qiagen). Data were analyzed using the 2^−ΔΔCT method. Data were normalized so the average of the saline group was 1.

Pharmacological intervention - behavioral studies

As global FAAH inhibition is associated with suppression of colonic inflammation [89–97], we administered the FAAH inhibitor intracerebroventricularly (icv) to be able to establish the importance of central FAAH inhibition on colitis-induced anxiety. Rats underwent intracranial cannulations as previously described [50]. Briefly, under isoflurane anesthesia and analgesic treatment (meloxicam (1 mg·kg⁻¹, subcutaneously)), rats were implanted with a 12 mm unilateral cannula into the lateral ventricle (coordinates: −0.90 mm anteroposterior, 1.4 mm mediolateral, and −2.8 mm dorsoventral from Bregma). Rats were given one week of recovery before colitis induction, and as in the previous experiments, anxiety-like behavior was tested 7 days later. On the three consecutive days before drug infusion and testing, rats were exposed to daily mock infusions. Two hours prior to EPM testing, animals received icv infusions (2 µL; 1 µL/min) of solutions containing vehicle (0.9% saline:dimethylsulfoxide (DMSO):Tween-80 [80:10:10; vol:vol:vol]) or a FAAH inhibitor (PF-04457845 (PF); Pfizer, New York, NY, USA; 100 ng and 1 µg) [98–100]. Infusers extended 2 mm past guide cannula and were left in place 1 min following infusion. Two hours following drug administration all animals were tested for 5 min in the EPM as described above. Following testing, animals were euthanized and ventricular cannula placement was confirmed with dye infusion post-mortem.

Pharmacological intervention - biochemical studies

To understand the role of CRF signaling on the colitis-induced reductions of AEA signaling, we examined the impact of sustained disruption of CRF-R1 signaling during the entire duration of colitis (i.e., 7 days) utilizing continuous drug infusion with an osmotic mini-pump (Alzet, Cupertino, CA, USA; Model 2002; 0.5 µL/h) connected to a 5 mm cannula (Alzet, Brain Infuser Kit 2) [101]. The osmotic mini-pumps were pre-loaded with vehicle (artificial cerebral spinal fluid [102]: DMSO [90:10; vol:vol]) or a CRF-R1 antagonist (antalarmin (Cayman Chemical Company, 15147); 10 µg/day) [103] and were incubated at 37 °C submerged in sterile physiological saline for 1–3 days prior to implantation. Under isoflurane anesthesia and analgesic (meloxicam (1 mg·kg⁻¹, subcutaneously)) treatment, the unilateral cannula was placed into the lateral ventricle, −0.90 mm anteroposterior and 1.4 mm mediolateral from Bregma, and the pump was placed subcutaneously. Surgeries were performed on the same day, but prior to, TNBS or saline administration. One week following surgery and colitis onset, brain regions were isolated as described above for eCB analysis. Ventricular cannula placement was confirmed post-mortem with dye infusion.

Statistical analyses

All statistics were carried out using Prism v8. For comparison of two groups, one-tailed (phenotypic confirmation of damage, corticosterone and anxiety-like behavior) or two-tailed Student’s t tests were used (remaining data, including correlations). For comparison of repeated measures, a repeated measure analysis of variance (ANOVA) or mixed-effect analysis was performed. For comparisons between two independent variables, two-way ANOVAs were performed. For all ANOVA analyses, significant interactions and main effects were reported, and specific group comparisons were made using Fisher’s Least Significant Difference tests. Planned comparisons based on a priori hypothesis were performed using independent t tests. t- or F-values, p values and eta squared (R²) are reported, as well as Pearson correlation coefficients (r) (weak = 0.1 < 0.3; moderate = 0.3 < 0.05; strong = 0.5 < 0.7; very strong = >0.7). Data are presented as mean ± standard error of the mean (SEM). Outliers were removed using the ROUT method [104], set to a 1% threshold, as previously described [83]. p < 0.05 was considered statistically significant. Detailed statistics for data represented in figures, as well as correlation values, are reported in Tables S2–4.

Results

Colitis induction produced behavioral indices of increased anxiety-like behavior

Data presented on colitis phenotype (i.e., weight loss, macroscopic tissue damage and MPO activity; Fig. 1A–C) are a representative set of data from the rats used for AEA and 2-AG analysis, but these effects were consistent across all experimental cohorts. Animals administered TNBS lost weight between Day 0 and Day 3 but started gaining it again thereafter (Fig. 1A); whereas controls gained weight daily. There were no differences at baseline between saline and TNBS-treated animals, but TNBS-treated animals weighed less than saline-treated animals all other days (Fig. 1A).

Rats administered TNBS also show an increase in colonic inflammation as measured by macroscopic tissue damage (Fig. 1B) and MPO activity (Fig. 1C) 7 days after treatment. Together these results indicate that peak weight loss occurred at Day 3, and gut inflammation was sustained at Day 7 after treatment.

Before initiating behavioral tasks, we wanted to verify that there would be no locomotor deficits (Fig. 1D), as reductions in locomotor activity can be a significant confound in behavioral tests of anxiety [105]. Using a mixed-effect model to analyze, we found that animals in both saline and TNBS groups had reduced locomotor activity after the first test day, likely due to habituation to the task. Animals administered TNBS showed reduced activity at Days 3 and 5 compared to saline-treated rats, but this difference was not present at baseline or Day 7. TNBS-treated animals also exhibited an elevation in circulating levels of corticosterone (Fig. 1E), the hormonal endpoint of the HPA axis, at Day 7. Corticosterone levels were strongly positively correlated with damage. Based on these results, we proceeded with anxiety-like behavior testing on Day 7, as at this time point animals showed no locomotor deficits, but TNBS-treated animals had sustained gut inflammation.

In the EPM, TNBS-treated animals had increased anxiety-like behavior as indicated by a reduction in the time spent in the open arms, increased time spent in the closed arms and reduction in head dips (Fig. 2A, B, H). There were no changes in open arm entries, closed arm entries, total arm entries, latency to enter open arms, or stretch attend postures (Fig. 2C–G). There was no correlation between damage score and any of these measures.

Fig. 2 — At Day 7 post-trinitrobenzene sulfonic acid (TNBS) administration there was an increase in anxiety-like behavior as indicated by a (A) reduction in time spent in the open arms, (B) increase in time spent in the closed arms and (H) a reduction in head dips; however, there were no effects on (C) open arm entries, (D) closed arm entries, (E) total arm entries, (F) latency to open arm or (G) stretch attend postures. n = 14–15/group. *p < 0.05 t test saline vs. TNBS. Saline = left, black bars with circles. TNBS = right, orange bars with squares.

TNBS-induced colitis altered central endocannabinoid levels

In order to investigate the role of the eCB system on colitis-induced anxiety-like behavior, we analyzed whether the eCB system was altered in Day 7 TNBS-treated rats. We found that AEA levels were reduced in the amygdala, medial prefrontal cortex and hippocampus but not in the hypothalamus in animals treated with TNBS (Fig. 3A–D). AEA levels, overall, were moderately or strongly, negatively correlated with macroscopic tissue damage, except in the hypothalamus. Concomitantly, TNBS treatment led to an increase in the hydrolytic activity of AEA’s metabolic enzyme, FAAH (V_max), in the amygdala and medial prefrontal cortex, but not in the hypothalamus or hippocampus (Fig. 3E–H). TNBS treatment resulted in no differences in the binding affinity of AEA for FAAH (K_m) (Table S3) in the amygdala, hypothalamus or hippocampus; however, animals with colitis had an increase in K_m in the medial prefrontal cortex. Similar to AEA levels, FAAH hydrolytic activity, but not binding affinity, overall, was strongly, but positively, correlated with damage score, particularly in the amygdala and medial prefrontal cortex. These data indicate that colitis is associated with an increase in corticolimbic FAAH-activity and a decline in the pool of AEA.

Fig. 3 — Following trinitrobenzene sulfonic acid (TNBS) administration, at Day 7, anandamide (AEA) levels were reduced in the (A) amygdala, (B) medial prefrontal cortex and (D) hippocampus, but not the (C) hypothalamus. Concomitantly, there was an increase in AEA’s metabolic enzyme’s (fatty acid amide hydrolase (FAAH)) activity (V_max), in the (E) amygdala, (F) medial prefrontal cortex, with no differences in the (H) hippocampus or (G) hypothalamus. In contrast to AEA levels, Day 7 2-arachindonylyl glycerol (2-AG) levels were increased in the (J) medial prefrontal cortex, (L) hippocampus, and no significant changes occurred in the (I) amygdala or (K) hypothalamus with TNBS administration. There were no differences at Day 7 post-administration in the activity of 2-AG’s metabolic enzyme (monoacylglycerol lipase (MAGL); V_max) in the (M) amygdala, (N) medial prefrontal cortex, (O) hypothalamus or (P) hippocampus from colitis. n = 9–12/group for levels and n = 4 = 6/group for enzyme activity. *p < 0.05, **p < 0.01, ****p < 0.0001, t test saline vs. TNBS. Saline = left, black bars with circles. TNBS = right, orange bars with squares.

In contrast to AEA levels, 2-AG levels were increased in the medial prefrontal cortex and hippocampus, but not significantly changed in the amygdala or hypothalamus (Fig. 3I–L), following TNBS administration. There was no impact of TNBS-colitis on the activity of 2-AG’s metabolic enzyme (V_max; Fig. 3M–P), MAGL, or its K_m (Table S3) in the amygdala, medial prefrontal cortex, hypothalamus or hippocampus. Overall, only hippocampal 2-AG was strongly, positively, correlated with damage; neither MAGL activity (excepting the hypothalamus) nor binding affinity correlated with damage score.

In addition, we examined the gene expression levels of a number of the molecular components of the eCB system (Table S4). There were no significant changes in any genes examined.

Central FAAH inhibition reversed colitis-induced anxiety-like behavior

To determine if the elevated FAAH activity and reduced AEA levels contributed to the increase in anxiety-like behavior, we examined if acute inhibition of FAAH, to elevate AEA signaling, would counter the colitis-induced anxiety. Given that FAAH activity was broadly increased following colitis, we opted to perform a central inhibition of FAAH to determine the impact of widespread central elevations in AEA signaling. We administered a FAAH inhibitor (PF) acutely at two doses and examined anxiety-like behavior in the EPM in order to investigate the relevance of changes in eCB levels to the increase in anxiety-like behavior.

Open arm time was reduced with TNBS-induced colitis and increased with administration of the FAAH inhibitor (Fig. 4A). Based on the outcomes of the initial experiments in this study, we made the a priori hypothesis that colitis would increase anxiety-like behavior and that treatment with a FAAH inhibitor would reverse that. Analysis of these planned comparisons demonstrated that, even following cranial surgery, there was a reduction in open arm time in TNBS-treated animals treated with saline vs. control animals treated with saline, supporting the robustness of this behavioral effect (as was seen in Fig. 2A). Administration of PF dose-dependently reversed the reduction of open arm time in the EPM; whereas 100 ng PF treatment in TNBS-treated animals partially reversed the anxiety phenotype (as it was no longer significantly different relative to vehicle-control animals, but not different from TNBS-vehicle animals), TNBS-treated animals treated with 1 μg PF exhibited significantly elevated time in the open arms relative to the TNBS-vehicle treated animals (Fig. 4A). We found that TNBS-treated rats had reduced open arm entries and head dips, but neither of these were influenced by administration of PF (Fig. 4C, G). There were no significant effects on closed arm time, closed arm entries, total arm entries or open arm latency as a result of TNBS-treatment or PF administration (Fig. 4B, D–F).

Macroscopic damage of the colon was increased in TNBS-treated rats, but this was lower in the 1 µg PF dose compared to its vehicle (Fig. 4H). Specifically, there was a significant reduction in the 1 µg PF group in most scorable items, including ulceration score, diarrhea and bowel thickness (data not shown). MPO activity was also increased with TNBS-treated animals, but was not influenced by central administration of 1 µg PF (Table S2). In addition, in most indices measured, there were weak, negative correlations with damage score. Together these results indicate that central FAAH inhibition reverses colitis-induced suppression of open arm time and reduces macroscopic colonic tissue damage score.

Central CRF-R1 signaling regulates colitis-induced alterations in AEA

As increased FAAH activity was found to contribute to the generation of colitis-induced anxiety, and given previous work that showed that activation of CRF-R1 can induce FAAH hydrolysis of AEA during psychological stress [50, 106], we examined CRF signaling as a potential upstream mechanism in our model [68].

We investigated if blocking central CRF-R1 with an antagonist, antalarmin, for the 7-days post-TNBS administration altered colitis-induced changes in AEA levels. While this caused no changes to TNBS-induced increases in macroscopic tissue damage (Table S2), antalarmin reversed colitis-induced reductions in AEA levels (Fig. 5A, D) in the amygdala and hippocampus. As in Fig. 3C, there was no effect of TNBS on hypothalamic AEA levels, nor was there an effect of antalarmin (Fig. 5C). In the medial prefrontal cortex, antalarmin alone reduced AEA levels, but did not alter TNBS-induced changes in AEA levels (Fig. 5B). CRF-R1 antagonism had no effect on 2-AG levels in the amygdala, hypothalamus and hippocampus (Fig. 5E, G, H). However, in the medial prefrontal cortex (Fig. 5F), antalarmin administration in saline animals increased 2-AG but did not alter 2-AG levels in the TNBS-treated animals. No overall pattern emerged with regards to correlation with macroscopic damage. Together these data demonstrated that the colitis-induced reductions in AEA, at least within the amygdala and hippocampus, were driven through CRF-R1 signaling.

Fig. 5 — Antalarmin (an antagonist for the corticotropin releasing factor receptor type 1 (CRF-R1)) reversed the colitis-induced reduction in anandamide (AEA) levels in the (A) amygdala and (D) hippocampus. In the (C) hypothalamus, there was no TNBS effect (as in Fig. 3C), and no effect of antalarmin. In the (B) medial prefrontal cortex, there was an interesting effect where antalarmin in the saline animals reduced AEA levels, but did not alter the TNBS-induced reduction of AEA levels. However, antalarmin had no effect on 2-arachidonylglycerol (2-AG) levels in the (E) amygdala, (G) hypothalamus or (H) hippocampus; however, in the (F) medial prefrontal cortex, antalarmin increased 2-AG levels in saline animals, but did not alter 2-AG levels in TNBS animals. n = 10–12/group. *p < 0.05 saline vs. TNBS of same treatment, ♦ p < 0.05, ♦♦♦ p < 0.001 vs. vehicle of same condition. Saline = left, black bars with circles. TNBS = right, orange bars with squares. Vehicle = left of each pair, filled bars. Antalarmin = right of each pair, open bars.

TNBS-colitis also reduced central AEA levels in female rats

Comorbid anxiety with IBD is not restricted to males and is also observed in females [16, 27]. To this end, we examined if there was a similar alteration in the eCB system as a result of TNBS administration in female rats in order to understand potential generalizability across sexes of the phenomenon we have demonstrated. Female rats also showed an increase in macroscopic tissue damage and MPO activity. Similar to male rats, there was a reduction (although smaller) of AEA levels in the medial prefrontal cortex (Fig. S1B) and no change in the hypothalamus (Fig. S1C), but reductions seen in males in the amygdala and hippocampus (p > 0.05) (Fig. S1AD) were not seen. Also, in contrast to male levels, there were no alterations (p > 0.05) in 2-AG levels in any of these areas (Fig. S1E–H). Unlike what was seen in males, neither AEA nor 2-AG levels were correlated with macroscopic damage.

Discussion

We demonstrate that the TNBS-model of colitis in rats, consistent with other rodent models of colitis [70–73, 107–109], produces an increase of anxiety-like behavior (Fig. 2), similar to the well-established comorbidity of colitis and anxiety in humans [1–5, 22, 27]. Colitis also resulted in an increase in FAAH-mediated hydrolysis of AEA across corticolimbic structures (Fig. 3) important for the regulation of affective behavior [105]. The magnitude of reductions in AEA and increases in FAAH activity is overall correlated with macroscopic damage, suggesting that the greater the disease severity the larger the impact on FAAH and AEA. This reduction in AEA signaling was mediated by central CRF-R1 (Fig. 5), and it contributed to the development of colitis-induced anxiety, as this was reversed by central inhibition of FAAH (Fig. 4). Together these data indicate that sustained peripheral inflammation can modulate affective behavior through an attenuation of central AEA signaling, which is driven by a recruitment of stress-responsive signaling systems. As such, this would suggest that inhibition of FAAH could represent a novel therapeutic approach to managing comorbid anxiety in peripheral inflammatory diseases.

Endocannabinoid signaling is well established to regulate affective behavioral processes such as anxiety through actions localized within the amygdala, medial prefrontal cortex and hippocampus [43, 110]. The current data extend these findings to demonstrate that a sustained inflammatory state results in a loss of central AEA signaling that contributes to the development of anxiety. Previous work has suggested that AEA and FAAH may be involved in behavioral changes produced by inflammation. For example, administration of the viral mimetic poly I:C produces changes in thermoregulation, pain sensitivity and anxiety, which are reversed by administration of a FAAH inhibitor [111]. In addition, acute early life inflammatory events have been shown to reduce social behavior during adolescence, a process that is also reversible through pharmacological inhibition of FAAH [112]. The current data, however, are the first demonstration that a sustained peripheral inflammatory insult reduces AEA levels and increases FAAH activity via central CRF-R1 activity, to increase anxiety, and thereby provides a putative model by which peripheral inflammation can modulate the central regulation of affective behavior.

Recent work from our group shows that both male and female mice exhibit anxiety-like behavior in a dextran sulfate sodium model of colitis [73]. Here we show in males that anxiety-like behavior induced by TNBS colitis is mediated through an CRF-R1 suppression of AEA levels. We also demonstrate in female rats that TNBS administration leads to a reduction of AEA levels, albeit to a lesser magnitude than in the males. It is possible that in females this reduction of AEA levels also contributes to the anxiety like-behavior observed across models, as previous work has demonstrated a correlation between AEA levels and anxiety-like behavior [113]; and, the difference in magnitude of AEA changes between sexes may contribute to the sex differences in anxiety-like behavior previously observed [73].

The finding that CRF-R1 activity mediates the colitis-induced reduction in AEA content broadens previous work indicating that CRF and FAAH exhibit an intricate relationship in the regulation of affective behavior [50, 106]. Chronic exposure to glucocorticoids results in sustained elevations in central FAAH hydrolysis and this is mediated by the elevated CRF/CRF-R1 activity as this effect of glucocorticoids is blocked by continuous administration of a CRF-R1 antagonist and is replicated by genetic overexpression of forebrain Crh [50, 106]. Inflammation is well-established to increase drive on the HPA axis, likely in an auto-regulatory manner where the elevations in potent anti-inflammatory glucocorticoids act to dampen inflammation itself [35, 114, 115]. Consistent with this, our data replicate previous studies [116, 117] showing that TNBS-colitis results in chronic elevations in corticosterone secretion, which is in line with the established increase in central Crh expression in rodent models of gut inflammation [54, 57, 59, 66, 67, 69, 89]. These data would suggest colitis-induced inflammation produces sustained adrenocortical responses, which result in the upregulation of CRF levels in the brain, producing an increase in FAAH activity and a reduction in AEA signaling. Consistent with previous work [50], this effect of glucocorticoids and CRF-R1 signaling on FAAH does not appear to be mediated by transcriptional changes in gene expression.

An unexpected finding of this study was that acute central inhibition of FAAH reduced the severity of colitis. Endocannabinoids are well-established anti-inflammatory molecules [118, 119], and FAAH inhibitors have been repeatedly found to be capable of reducing multiple aspects of gut inflammation across several animal models [89–91, 96, 120, 121]. While these anti-inflammatory effects of AEA signaling in colitis are largely due to peripheral actions on colonic tissue directly or local immune cells, there is evidence that central cannabinoid type 1 receptors (CB1) contribute to reducing inflammation in colitis [122]. It is also possible that PF entered the circulation, elevating AEA levels outside of the brain to influence the damage score. That said, the magnitude of reduction of colitis damage in the current study from central FAAH inhibition was relatively minor. Regardless, these data support previous findings that central FAAH inhibition is capable of modulating colonic inflammation.

In addition to reduced AEA, we also found that colitis was associated with elevations in 2-AG throughout several corticolimbic structures (Fig. 2). Prolonged elevations in CRF signaling have been found to produce elevations in tissue 2-AG levels [106]. This effect was not as robust as the reduction in AEA, as it was largely lost following cannulation surgery, and not seen in females. Unlike the reductions in AEA, the relevance of these increases in 2-AG during colitis has yet to be elucidated. As stress-induced elevations in 2-AG signaling have been proposed to produce both anxiolytic and anxiogenic effects [43], future work is required to examine this question in more depth.

We did not investigate which receptors mediate the anxiolytic effect observed herein. Previous work with psychological stress points to a role for CB1 in this regard [43]. AEA’s anxiolytic effect seems to be due to its signaling at the CB1 receptor [43]. Furthermore, differently from AEA, the ability of 2-AG to buffer anxiety is linked to signaling at the CB1 receptor, but also the CB2 receptor [123–126]. Given our anxiolytic effect was observed with FAAH inhibition, which elevates AEA and not 2-AG, it was likely through a CB1 mechanism; however, future work will have to elucidate these specifics, especially as AEA can also act on the transient receptor potential cation channel subfamily V member 1 (TRPV1) and peroxisome proliferator-activated receptors (PPARs). More so, FAAH also metabolizes oleoylethanolamide (OEA) and palmitoylethanolamide (PEA) which have also been implicated in anxiety and inflammation [127–133].

Together, these data demonstrate that the induction of colitis results in a suppression of central AEA signaling via a CRF-R1 mediated increase in FAAH activity, which then promotes the development of anxiety. Given the similarities seen to chronic stress and glucocorticoid exposure [50, 106], this suggests that compromised central AEA signaling may be a broad mechanism favoring the development of anxiety in response to a host of psychological or physiological insults, particularly those that produce increased demand on the HPA axis. As such, these data would support the investigation of FAAH inhibitors as a treatment approach in chronic inflammatory disease states, both for the inflammatory pathology itself but also the psychiatric comorbidities. FAAH inhibitors have already been established in humans to reduce anxiety that develops during cannabis withdrawal [134], dampen the subjective and physiological responses to stress [135] and produce clinically relevant anxiolysis in social anxiety disorder [136], indicating their feasibility and potential efficacy for the management of affective disturbances in humans. In line with this, many individuals with chronic inflammatory diseases use cannabis which is associated with broad improvements in affective state and quality of life [137, 138], suggesting that cannabinoids may also have some therapeutic value in this domain. Therefore, there is potential for FAAH inhibition on both the primary outcomes of inflammatory diseases, as well as comorbid psychiatric issues and quality of life measures, serving as a dual-pronged therapeutic.

Funding and disclosures

This work was supported by grants from the Canadian Institutes of Health Research (CIHR; FDN333950-MNH; FDN148380-KAS; PJT159454-QJP, MH, KAS); Alberta Innovates Health Solutions (AIHS) CRIO Project 201200828-QJP, KAS. HAV received stipend funding from CIHR (Vanier CGS), University of Calgary (UofC; Killam Pre-doctoral Laureate), AIHS and Branch Out Neurological Foundation (BONF); MM received fellowship support from AIHS and CIHR; VC received a studentship from UofC; KT received studentships from the National Sciences and Engineering Research Council (NSERC) and AIHS; KL received a studentship from BONF; AS received salary support from the UofC Mathison Centre for Mental Health Research and Education. MNH is the recipient of a Tier II Canada Research Chair. KAS holds the Crohn’s and Colitis Canada Chair in IBD Research at the UofC. Funding agencies had no influence on the design, execution or publishing of this work. MNH is a scientific advisor for Sophren Therapeutics and Lundbeck. All other authors have no disclosures to report.

Supplementary information

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Supplemental Table 1^{(15.4KB, docx)}

Supplemental Table 2^{(25.8KB, xlsx)}

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Supplemental Figure 1^{(624.7KB, pdf)}

Acknowledgements

We acknowledge that this work was conducted on the traditional territories of the people of the Treaty 7 region in Southern Alberta, which includes the Blackfoot Confederacy (comprising the Siksika, Piikani, and Kainai First Nations), as well as the Tsuut’ina First Nation, and the Stoney Nakoda (including the Chiniki, Bearspaw, and Wesley First Nations). The City of Calgary is also home to Métis Nation of Alberta, Region III. Mass spectrometry processing was performed at the Southern Alberta Mass Spectrometry Facility. We acknowledge the work of the University of Calgary Health Sciences Animal Research Centre, particularly Krista Jensen and Brittany Munro. PF-04457845 was gifted from Pfizer, who had no influence on the design, execution or publishing of this work. Aspects of this work appear in the following doctoral thesis by HAV: “Investigating the Role of Central Endocannabinoids and Inflammation in Comorbid Anxiety-Like Behaviour and Colitis,” University of Calgary, 2020.

Author contributions

HAV, CMK, QJP, KAS, and MNH were involved in the design of the manuscript. HAV, MM, CMK, VC, KT, MQ, KL, AS, and MNH performed experiments. HAV, CMK, QJP, KAS, and MNH analyzed data. HAV prepared figures. HAV, QJP, KAS, and MNH wrote the manuscript with input from all authors.

Footnotes

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Haley A. Vecchiarelli, Email: haleyvecchiarelli@uvic.ca

Matthew N. Hill, Email: mnhill@ucalgary.ca

Supplementary information

Supplementary Information accompanies this paper at (10.1038/s41386-020-00939-7).

References

1.Marrie RA, Walld R, Bolton JM, Sareen J, Patten SB, Singer A, et al. Psychiatric comorbidity increases mortality in immune-mediated inflammatory diseases. Gen Hosp Psychiatry. 2018;53:65–72. doi: 10.1016/j.genhosppsych.2018.06.001. [DOI] [PubMed] [Google Scholar]
2.Bernstein CN, Hitchon CA, Walld R, Bolton JM, Sareen J, Walker JR, et al. Increased burden of psychiatric disorders in inflammatory bowel disease. Inflamm Bowel Dis. 2019;25:360–8. doi: 10.1093/ibd/izy235. [DOI] [PMC free article] [PubMed] [Google Scholar]
3.Moulton CD, Pavlidis P, Norton C, Norton S, Pariante C, Hayee B, et al. Depressive symptoms in inflammatory bowel disease: an extraintestinal manifestation of inflammation? Clin Exp Immunol. 2019;197:308–18. doi: 10.1111/cei.13276. [DOI] [PMC free article] [PubMed] [Google Scholar]
4.Whitehouse CE, Fisk JD, Bernstein CN, Berrigan LI, Bolton JM, Graff LA, et al. Comorbid anxiety, depression, and cognition in MS and other immune-mediated disorders. Neurology. 2019;92:e406–17. doi: 10.1212/WNL.0000000000006854. [DOI] [PMC free article] [PubMed] [Google Scholar]
5.Thomann AK, Mak JWY, Zhang JW, Wuestenberg T, Ebert MP, Sung JJY, et al. Review article: bugs, inflammation and mood-a microbiota-based approach to psychiatric symptoms in inflammatory bowel diseases. Aliment Pharm Ther. 2020;52:247–66. doi: 10.1111/apt.15787. [DOI] [PubMed] [Google Scholar]
6.Gracie DJ, Irvine AJ, Sood R, Mikocka-Walus A, Hamlin PJ, Ford AC. Effect of psychological therapy on disease activity, psychological comorbidity, and quality of life in inflammatory bowel disease: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2017;2:189–99. doi: 10.1016/S2468-1253(16)30206-0. [DOI] [PubMed] [Google Scholar]
7.Jones JL, Nguyen GC, Benchimol EI, Bernstein CN, Bitton A, Kaplan GG, et al. The impact of inflammatory bowel disease in Canada 2018: quality of life. J Can Assoc Gastroenterol. 2019;2:S42–S48.. doi: 10.1093/jcag/gwy048. [DOI] [PMC free article] [PubMed] [Google Scholar]
8.Porcelli P, Leoci C, Guerra V. A prospective study of the relationship between disease activity and psychologic distress in patients with inflammatory bowel disease. Scand J Gastroenterol. 1996;31:792–6. doi: 10.3109/00365529609010354. [DOI] [PubMed] [Google Scholar]
9.Addolorato G, Capristo E, Stefanini GF, Gasbarrini G. Inflammatory bowel disease: a study of the association between anxiety and depression, physical morbidity, and nutritional status. Scand J Gastroenterol. 1997;32:1013–21. doi: 10.3109/00365529709011218. [DOI] [PubMed] [Google Scholar]
10.Fuller-Thomson E, Sulman J. Depression and inflammatory bowel disease: findings from two nationally representative Canadian surveys. Inflamm Bowel Dis. 2006;12:697–707. doi: 10.1097/00054725-200608000-00005. [DOI] [PubMed] [Google Scholar]
11.Kovács Z, Kovács F. Depressive and anxiety symptoms, dysfunctional attitudes and social aspects in irritable bowel syndrome and inflammatory bowel disease. Int J Psychiatry Med. 2007;37:245–55. doi: 10.2190/PM.37.3.a. [DOI] [PubMed] [Google Scholar]
12.Lerebours E, Gower-Rousseau C, Merle V, Brazier F, Debeugny S, Marti R, et al. Stressful life events as a risk factor for inflammatory bowel disease onset: a population-based case-control study. Am J Gastroenterol. 2007;102:122–31. doi: 10.1111/j.1572-0241.2006.00931.x. [DOI] [PubMed] [Google Scholar]
13.Walker JR, Ediger JP, Graff LA, Greenfeld JM, Clara I, Lix L, et al. The Manitoba IBD cohort study: a population-based study of the prevalence of lifetime and 12-month anxiety and mood disorders. Am J Gastroenterol. 2008;103:1989–97. doi: 10.1111/j.1572-0241.2008.01980.x. [DOI] [PubMed] [Google Scholar]
14.Hyphantis TN, Tomenson B, Bai M, Tsianos E, Mavreas V, Creed F. Psychological distress, somatization, and defense mechanisms associated with quality of life in inflammatory bowel disease patients. Dig Dis Sci. 2010;55:724–32. doi: 10.1007/s10620-009-0762-z. [DOI] [PubMed] [Google Scholar]
15.Filipovic BR, Filipovic BF. Psychiatric comorbidity in the treatment of patients with inflammatory bowel disease. World J Gastroenterol. 2014;20:3552–63. doi: 10.3748/wjg.v20.i13.3552. [DOI] [PMC free article] [PubMed] [Google Scholar]
16.Tribbick D, Salzberg M, Ftanou M, Connell WR, Macrae F, Kamm MA, et al. Prevalence of mental health disorders in inflammatory bowel disease: an Australian outpatient cohort. Clin Exp Gastroenterol. 2015;8:197–204. doi: 10.2147/CEG.S77567. [DOI] [PMC free article] [PubMed] [Google Scholar]
17.Fuller-Thomson E, Lateef R, Sulman J. Robust association between inflammatory bowel disease and generalized anxiety disorder: findings from a nationally representative Canadian Study. Inflamm Bowel Dis. 2015;21:2341–8. doi: 10.1097/MIB.0000000000000551. [DOI] [PubMed] [Google Scholar]
18.Fiest KM, Bernstein CN, Walker JR, Graff LA, Hitchon CA, Peschken CA, et al. Systematic review of interventions for depression and anxiety in persons with inflammatory bowel disease. BMC Res Notes. 2016;9:404. doi: 10.1186/s13104-016-2204-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
19.Mikocka-Walus A, Knowles SR, Keefer L, Graff L. Controversies revisited: a systematic review of the comorbidity of depression and anxiety with inflammatory bowel diseases. Inflamm Bowel Dis. 2016;22:752–62. doi: 10.1097/MIB.0000000000000620. [DOI] [PubMed] [Google Scholar]
20.Neuendorf R, Harding A, Stello N, Hanes D, Wahbeh H. Depression and anxiety in patients with inflammatory bowel disease: a systematic review. J Psychosom Res. 2016;87:70–80. doi: 10.1016/j.jpsychores.2016.06.001. [DOI] [PubMed] [Google Scholar]
21.Byrne G, Rosenfeld G, Leung Y, Qian H, Raudzus J, Nunez C, et al. Prevalence of anxiety and depression in patients with inflammatory bowel disease. Can J Gastroenterol Hepatol. 2017;2017:6496727. doi: 10.1155/2017/6496727. [DOI] [PMC free article] [PubMed] [Google Scholar]
22.Marrie RA, Walld R, Bolton JM, Sareen J, Walker JR, Patten SB, et al. Increased incidence of psychiatric disorders in immune-mediated inflammatory disease. J Psychosom Res. 2017;101:17–23. doi: 10.1016/j.jpsychores.2017.07.015. [DOI] [PubMed] [Google Scholar]
23.Regueiro M, Greer JB, Szigethy E. Etiology and treatment of pain and psychosocial issues in patients with inflammatory bowel diseases. Gastroenterology. 2017;152:430–9.e4. doi: 10.1053/j.gastro.2016.10.036. [DOI] [PubMed] [Google Scholar]
24.Bhamre R, Sawrav S, Adarkar S, Sakaria RJ, Bhatia S. Psychiatric comorbidities in patients with inflammatory bowel disease. Indian J Gastroenterol. 2018;37:307–12. doi: 10.1007/s12664-018-0870-9. [DOI] [PubMed] [Google Scholar]
25.Navabi S, Gorrepati VS, Yadav S, Chintanaboina J, Maher S, Demuth P, et al. Influences and impact of anxiety and depression in the setting of inflammatory bowel disease. Inflamm Bowel Dis. 2018;24:2303–8. doi: 10.1093/ibd/izy143. [DOI] [PubMed] [Google Scholar]
26.Choi K, Chun J, Han K, Park S, Soh H, Kim J, et al. Risk of anxiety and depression in patients with inflammatory bowel disease: a nationwide, population-based study. J Clin Med. 2019;8:654. doi: 10.3390/jcm8050654. [DOI] [PMC free article] [PubMed] [Google Scholar]
27.Lewis K, Marrie RA, Bernstein CN, Graff LA, Patten SB, Sareen J, et al. The prevalence and risk factors of undiagnosed depression and anxiety disorders among patients with inflammatory bowel disease. Inflamm Bowel Dis. 2019;25:1674–80. doi: 10.1093/ibd/izz045. [DOI] [PubMed] [Google Scholar]
28.Narula N, Pinto-Sanchez MI, Calo NC, Ford AC, Bercik P, Reinisch W, et al. Anxiety but not depression predicts poor outcomes in inflammatory bowel disease. Inflamm Bowel Dis. 2019;25:1255–61. doi: 10.1093/ibd/izy385. [DOI] [PubMed] [Google Scholar]
29.Thakur ER, Sansgiry S, Kramer JR, Waljee AK, Gaidos JK, Feagins LA, et al. The incidence and prevalence of anxiety, depression, and post-traumatic stress disorder in a national cohort of US Veterans With Inflammatory Bowel Disease. Inflamm Bowel Dis. 2020;26:1423–8. doi: 10.1093/ibd/izz280. [DOI] [PMC free article] [PubMed] [Google Scholar]
30.Walker EA, Gelfand AN, Gelfand MD, Katon WJ. Psychiatric diagnoses, sexual and physical victimization, and disability in patients with irritable bowel syndrome or inflammatory bowel disease. Psychol Med. 1995;25:1259–67. doi: 10.1017/S0033291700033225. [DOI] [PubMed] [Google Scholar]
31.Sewitch MJ, Abrahamowicz M, Bitton A, Daly D, Wild GE, Cohen A, et al. Psychological distress, social support, and disease activity in patients with inflammatory bowel disease. Am J Gastroenterol. 2001;96:1470–9. doi: 10.1111/j.1572-0241.2001.03800.x. [DOI] [PubMed] [Google Scholar]
32.Guthrie E, Jackson J, Shaffer J, Thompson D, Tomenson B, Creed F. Psychological disorder and severity of inflammatory bowel disease predict health-related quality of life in ulcerative colitis and Crohn’s disease. Am J Gastroenterol. 2002;97:1994–9. doi: 10.1111/j.1572-0241.2002.05842.x. [DOI] [PubMed] [Google Scholar]
33.Casellas F, Arenas JI, Baudet JS, Fábregas S, García N, Gelabert J, et al. Impairment of health-related quality of life in patients with inflammatory bowel disease: a Spanish multicenter study. Inflamm Bowel Dis. 2005;11:488–96. doi: 10.1097/01.MIB.0000159661.55028.56. [DOI] [PubMed] [Google Scholar]
34.Graff LA, Walker JR, Lix L, Clara I, Rawsthorne P, Rogala L, et al. The relationship of inflammatory bowel disease type and activity to psychological functioning and quality of life. Clin Gastroenterol Hepatol. 2006;4:1491–501. doi: 10.1016/j.cgh.2006.09.027. [DOI] [PubMed] [Google Scholar]
35.Bonaz BL, Bernstein CN. Brain-gut interactions in inflammatory bowel disease. Gastroenterology. 2013;144:36–49. doi: 10.1053/j.gastro.2012.10.003. [DOI] [PubMed] [Google Scholar]
36.Mulak A, Bonaz B. Irritable bowel syndrome: a model of the brain-gut interactions. Med Sci Monit. 2004;10:RA55–62. [PubMed] [Google Scholar]
37.Reber SO. Stress and animal models of inflammatory bowel disease–an update on the role of the hypothalamo-pituitary-adrenal axis. Psychoneuroendocrinology. 2012;37:1–19. doi: 10.1016/j.psyneuen.2011.05.014. [DOI] [PubMed] [Google Scholar]
38.Sharkey KA, Wiley JW. The role of the endocannabinoid system in the brain-gut axis. Gastroenterology. 2016;151:252–66. doi: 10.1053/j.gastro.2016.04.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
39.Nestler EJ, Barrot M, DiLeone RJ, Eisch AJ, Gold SJ, Monteggia LM. Neurobiology of depression. Neuron. 2002;34:13–25. doi: 10.1016/S0896-6273(02)00653-0. [DOI] [PubMed] [Google Scholar]
40.Tafet GE, Nemeroff CB. The links between stress and depression: psychoneuroendocrinological, genetic, and environmental interactions. J Neuropsychiatry Clin Neurosci. 2016;28:77–88. doi: 10.1176/appi.neuropsych.15030053. [DOI] [PubMed] [Google Scholar]
41.Hill MN, McEwen BS. Involvement of the endocannabinoid system in the neurobehavioural effects of stress and glucocorticoids. Prog Neuropsychopharmacol Biol Psychiatry. 2010;34:791–7. doi: 10.1016/j.pnpbp.2009.11.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
42.Hill MN, Tasker JG. Endocannabinoid signaling, glucocorticoid-mediated negative feedback, and regulation of the hypothalamic-pituitary-adrenal axis. Neuroscience. 2012;204:5–16. doi: 10.1016/j.neuroscience.2011.12.030. [DOI] [PMC free article] [PubMed] [Google Scholar]
43.Morena M, Patel S, Bains JS, Hill MN. Neurobiological Interactions Between Stress and the Endocannabinoid System. Neuropsychopharmacology. 2016;41:80–102. doi: 10.1038/npp.2015.166. [DOI] [PMC free article] [PubMed] [Google Scholar]
44.Haller J, Bakos N, Szirmay M, Ledent C, Freund TF. The effects of genetic and pharmacological blockade of the CB1 cannabinoid receptor on anxiety. Eur J Neurosci. 2002;16:1395–8. doi: 10.1046/j.1460-9568.2002.02192.x. [DOI] [PubMed] [Google Scholar]
45.Haller J, Varga B, Ledent C, Freund TF. CB1 cannabinoid receptors mediate anxiolytic effects: convergent genetic and pharmacological evidence with CB1-specific agents. Behav Pharmacol. 2004;15:299–304. doi: 10.1097/01.fbp.0000135704.56422.40. [DOI] [PubMed] [Google Scholar]
46.Hill MN, Hillard CJ, McEwen BS. Alterations in corticolimbic dendritic morphology and emotional behavior in cannabinoid CB1 receptor-deficient mice parallel the effects of chronic stress. Cereb Cortex. 2011;21:2056–64. doi: 10.1093/cercor/bhq280. [DOI] [PMC free article] [PubMed] [Google Scholar]
47.Patel S, Cravatt BF, Hillard CJ. Synergistic interactions between cannabinoids and environmental stress in the activation of the central amygdala. Neuropsychopharmacology. 2005;30:497–507. doi: 10.1038/sj.npp.1300535. [DOI] [PubMed] [Google Scholar]
48.Hill MN, McLaughlin RJ, Morrish AC, Viau V, Floresco SB, Hillard CJ, et al. Suppression of amygdalar endocannabinoid signaling by stress contributes to activation of the hypothalamic-pituitary-adrenal axis. Neuropsychopharmacology. 2009;34:2733–45. doi: 10.1038/npp.2009.114. [DOI] [PMC free article] [PubMed] [Google Scholar]
49.Hill MN, Kumar SA, Filipski SB, Iverson M, Stuhr KL, Keith JM, et al. Disruption of fatty acid amide hydrolase activity prevents the effects of chronic stress on anxiety and amygdalar microstructure. Mol Psychiatry. 2013;18:1125–35. doi: 10.1038/mp.2012.90. [DOI] [PMC free article] [PubMed] [Google Scholar]
50.Gray JM, Vecchiarelli HA, Morena M, Lee TTY, Hermanson DJ, Kim AB, et al. Corticotropin-releasing hormone drives anandamide hydrolysis in the amygdala to promote anxiety. J Neurosci. 2015;35:3879–92. doi: 10.1523/JNEUROSCI.2737-14.2015. [DOI] [PMC free article] [PubMed] [Google Scholar]
51.Rubino T, Realini N, Castiglioni C, Guidali C, Viganó D, Marras E, et al. Role in anxiety behavior of the endocannabinoid system in the prefrontal cortex. Cereb Cortex. 2008;18:1292–301. doi: 10.1093/cercor/bhm161. [DOI] [PubMed] [Google Scholar]
52.Campos AC, Brant F, Miranda AS, Machado FS, Teixeira AL. Cannabidiol increases survival and promotes rescue of cognitive function in a murine model of cerebral malaria. Neuroscience. 2015;289:166–80. doi: 10.1016/j.neuroscience.2014.12.051. [DOI] [PubMed] [Google Scholar]
53.de la Tremblaye PB, Benoit SM, Schock S, Plamondon H. CRHR1 exacerbates the glial inflammatory response and alters BDNF/TrkB/pCREB signaling in a rat model of global cerebral ischemia: implications for neuroprotection and cognitive recovery. Prog Neuropsychopharmacol Biol Psychiatry. 2017;79:234–48. doi: 10.1016/j.pnpbp.2017.06.021. [DOI] [PubMed] [Google Scholar]
54.Ji G, Fu Y, Ruppert KA, Neugebauer V. Pain-related anxiety-like behavior requires CRF1 receptors in the amygdala. Mol Pain. 2007;3:13. doi: 10.1186/1744-8069-3-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
55.Fu Y, Neugebauer V. Differential mechanisms of CRF1 and CRF2 receptor functions in the amygdala in pain-related synaptic facilitation and behavior. J Neurosci. 2008;28:3861–76. doi: 10.1523/JNEUROSCI.0227-08.2008. [DOI] [PMC free article] [PubMed] [Google Scholar]
56.O’Malley D, Quigley EMM, Dinan TG, Cryan JF. Do interactions between stress and immune responses lead to symptom exacerbations in irritable bowel syndrome? Brain Behav Immun. 2011;25:1333–41. doi: 10.1016/j.bbi.2011.04.009. [DOI] [PubMed] [Google Scholar]
57.Taché Y. Corticotrophin-releasing factor 1 activation in the central amygdale and visceral hyperalgesia. Neurogastroenterol Motil. 2015;27:1–6. doi: 10.1111/nmo.12495. [DOI] [PMC free article] [PubMed] [Google Scholar]
58.Schäfer M, Mousa SA, Stein C. Corticotropin-releasing factor in antinociception and inflammation. Eur J Pharmacol. 1997;323:1–10. doi: 10.1016/S0014-2999(97)00057-5. [DOI] [PubMed] [Google Scholar]
59.Bravo JA, Dinan TG, Cryan JF. Alterations in the central CRF system of two different rat models of comorbid depression and functional gastrointestinal disorders. Int J Neuropsychopharmacol. 2011;14:666–83. doi: 10.1017/S1461145710000994. [DOI] [PubMed] [Google Scholar]
60.Hubbard CS, Labus JS, Bueller J, Stains J, Suyenobu B, Dukes GE, et al. Corticotropin-releasing factor receptor 1 antagonist alters regional activation and effective connectivity in an emotional-arousal circuit during expectation of abdominal pain. J Neurosci. 2011;31:12491–500. doi: 10.1523/JNEUROSCI.1860-11.2011. [DOI] [PMC free article] [PubMed] [Google Scholar]
61.Labus JS, Hubbard CS, Bueller J, Ebrat B, Tillisch K, Chen M, et al. Impaired emotional learning and involvement of the corticotropin-releasing factor signaling system in patients with irritable bowel syndrome. Gastroenterology. 2013;145:1253–61.e1-3. doi: 10.1053/j.gastro.2013.08.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
62.Neurath M, Fuss I, Strober W. TNBS-colitis. Int Rev Immunol. 2000;19:51–62. doi: 10.3109/08830180009048389. [DOI] [PubMed] [Google Scholar]
63.Chassaing B, Aitken JD, Malleshappa M, Vijay-Kumar M. Dextran sulfate sodium (DSS)-induced colitis in mice. Curr Protoc Immunol. 2014;104:15.25.1–15.25.14. doi: 10.1002/0471142735.im1525s104. [DOI] [PMC free article] [PubMed] [Google Scholar]
64.Kiesler P, Fuss IJ, Strober W. Experimental models of inflammatory bowel diseases. Cell Mol Gastroenterol Hepatol. 2015;1:154–70. doi: 10.1016/j.jcmgh.2015.01.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
65.Antoniou E, Margonis GA, Angelou A, Pikouli A, Argiri P, Karavokyros I, et al. The TNBS-induced colitis animal model: An overview. Ann Med Surg. 2016;11:9–15. doi: 10.1016/j.amsu.2016.07.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
66.Kresse AE, Million M, Saperas E, Taché Y. Colitis induces CRF expression in hypothalamic magnocellular neurons and blunts CRF gene response to stress in rats. Am J Physiol Gastrointest Liver Physiol. 2001;281:G1203–1213. doi: 10.1152/ajpgi.2001.281.5.G1203. [DOI] [PubMed] [Google Scholar]
67.Kojima K, Naruse Y, Iijima N, Wakabayashi N, Mitsufuji S, Ibata Y, et al. HPA-axis responses during experimental colitis in the rat. Am J Physiol Regul Integr Comp Physiol. 2002;282:R1348–1355. doi: 10.1152/ajpregu.00260.2001. [DOI] [PubMed] [Google Scholar]
68.Porcher C, Sinniger V, Juhem A, Mouchet P, Bonaz B. Neuronal activity and CRF receptor gene transcription in the brains of rats with colitis. Am J Physiol Gastrointest Liver Physiol. 2004;287:G803–814. doi: 10.1152/ajpgi.00135.2004. [DOI] [PubMed] [Google Scholar]
69.Greenwood-Van Meerveld B, Johnson AC, Schulkin J, Myers DA. Long-term expression of corticotropin-releasing factor (CRF) in the paraventricular nucleus of the hypothalamus in response to an acute colonic inflammation. Brain Res. 2006;1071:91–96. doi: 10.1016/j.brainres.2005.11.071. [DOI] [PubMed] [Google Scholar]
70.Lyte M, Li W, Opitz N, Gaykema RPA, Goehler LE. Induction of anxiety-like behavior in mice during the initial stages of infection with the agent of murine colonic hyperplasia citrobacter rodentium. Physiol Behav. 2006;89:350–7. doi: 10.1016/j.physbeh.2006.06.019. [DOI] [PubMed] [Google Scholar]
71.Bercik P, Verdu EF, Foster JA, Macri J, Potter M, Huang X, et al. Chronic gastrointestinal inflammation induces anxiety-like behavior and alters central nervous system biochemistry in mice. Gastroenterology. 2010;139:2102–12.e1. doi: 10.1053/j.gastro.2010.06.063. [DOI] [PubMed] [Google Scholar]
72.Chen J, Winston JH, Fu Y, Guptarak J, Jensen KL, Shi X-Z, et al. Genesis of anxiety, depression, and ongoing abdominal discomfort in ulcerative colitis-like colon inflammation. Am J Physiol Regul Integr Comp Physiol. 2015;308:R18–27. doi: 10.1152/ajpregu.00298.2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
73.Nyuyki KD, Cluny NL, Swain MG, Sharkey KA, Pittman QJ. Altered brain excitability and increased anxiety in mice with experimental colitis: consideration of hyperalgesia and sex differences. Front Behav Neurosci. 2018;12:58. doi: 10.3389/fnbeh.2018.00058. [DOI] [PMC free article] [PubMed] [Google Scholar]
74.McCafferty DM, Sharkey KA, Wallace JL. Beneficial effects of local or systemic lidocaine in experimental colitis. Am J Physiol. 1994;266:G560–567. doi: 10.1152/ajpgi.1994.266.4.G560. [DOI] [PubMed] [Google Scholar]
75.Natah SS, Mouihate A, Pittman QJ, Sharkey KA. Disruption of the blood-brain barrier during TNBS colitis. Neurogastroenterol Motil. 2005;17:433–46. doi: 10.1111/j.1365-2982.2005.00654.x. [DOI] [PubMed] [Google Scholar]
76.Spencer SJ, Hyland NP, Sharkey KA, Pittman QJ. Neonatal immune challenge exacerbates experimental colitis in adult rats: potential role for TNF-alpha. Am J Physiol Regul Integr Comp Physiol. 2007;292:R308–315. doi: 10.1152/ajpregu.00398.2006. [DOI] [PubMed] [Google Scholar]
77.Riazi K, Galic MA, Kuzmiski JB, Ho W, Sharkey KA, Pittman QJ. Microglial activation and TNFalpha production mediate altered CNS excitability following peripheral inflammation. Proc Natl Acad Sci USA. 2008;105:17151–6. doi: 10.1073/pnas.0806682105. [DOI] [PMC free article] [PubMed] [Google Scholar]
78.da Silva MS, Sánchez-Fidalgo S, Talero E, Cárdeno A, da Silva MA, Villegas W, et al. Anti-inflammatory intestinal activity of Abarema cochliacarpos (Gomes) Barneby & Grimes in TNBS colitis model. J Ethnopharmacol. 2010;128:467–75. doi: 10.1016/j.jep.2010.01.024. [DOI] [PubMed] [Google Scholar]
79.Ikeda M, Takeshima F, Isomoto H, Shikuwa S, Mizuta Y, Ozono Y, et al. Simvastatin attenuates trinitrobenzene sulfonic acid-induced colitis, but not oxazalone-induced colitis. Dig Dis Sci. 2008;53:1869–75. doi: 10.1007/s10620-007-0102-0. [DOI] [PubMed] [Google Scholar]
80.Takagi T, Naito Y, Mizushima K, Akagiri S, Suzuki T, Hirata I, et al. Inhalation of carbon monoxide ameliorates TNBS-induced colitis in mice through the inhibition of TNF-α expression. Dig Dis Sci. 2010;55:2797–804. doi: 10.1007/s10620-009-1112-x. [DOI] [PubMed] [Google Scholar]
81.Cluny NL, Keenan CM, Duncan M, Fox A, Lutz B, Sharkey KA. Naphthalen-1-yl-(4-pentyloxynaphthalen-1-yl)methanone (SAB378), a peripherally restricted cannabinoid CB1/CB2 receptor agonist, inhibits gastrointestinal motility but has no effect on experimental colitis in mice. J Pharm Exp Ther. 2010;334:973–80. doi: 10.1124/jpet.110.169946. [DOI] [PubMed] [Google Scholar]
82.Morena M, Aukema RJ, Leitl KD, Rashid AJ, Vecchiarelli HA, Josselyn SA, et al. Upregulation of anandamide hydrolysis in the basolateral complex of amygdala reduces fear memory expression and indices of stress and anxiety. J Neurosci. 2019;39:1275–92. doi: 10.1523/JNEUROSCI.2251-18.2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
83.Vecchiarelli HA, Gandhi CP, Gray JM, Morena M, Hassan KI, Hill MN. Divergent responses of inflammatory mediators within the amygdala and medial prefrontal cortex to acute psychological stress. Brain Behav Immun. 2016;51:70–91. doi: 10.1016/j.bbi.2015.07.026. [DOI] [PubMed] [Google Scholar]
84.Vecchiarelli HA, Gandhi CP, Hill MN. Acute psychological stress modulates the expression of enzymes involved in the kynurenine pathway throughout corticolimbic circuits in adult male rats. Neural Plast. 2016;2016:7215684. doi: 10.1155/2016/7215684. [DOI] [PMC free article] [PubMed] [Google Scholar]
85.Hill MN, Karatsoreos IN, Hillard CJ, McEwen BS. Rapid elevations in limbic endocannabinoid content by glucocorticoid hormones in vivo. Psychoneuroendocrinology. 2010;35:1333–8. doi: 10.1016/j.psyneuen.2010.03.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
86.Qi M, Morena M, Vecchiarelli HA, Hill MN, Schriemer DC. A robust capillary liquid chromatography/tandem mass spectrometry method for quantitation of neuromodulatory endocannabinoids. Rapid Commun Mass Spectrom. 2015;29:1889–97. doi: 10.1002/rcm.7277. [DOI] [PubMed] [Google Scholar]
87.Atsak P, Morena M, Schoenmaker C, Tabak E, Oomen CA, Jamil S, et al. Glucocorticoid-endocannabinoid uncoupling mediates fear suppression deficits after early - Life stress. Psychoneuroendocrinology. 2018;91:41–49. doi: 10.1016/j.psyneuen.2018.02.021. [DOI] [PubMed] [Google Scholar]
88.Berger AL, Henricks AM, Lugo JM, Wright HR, Warrick CR, Sticht MA, et al. The lateral habenula directs coping styles under conditions of stress via recruitment of the endocannabinoid system. Biol Psychiatry. 2018;84:611–23. doi: 10.1016/j.biopsych.2018.04.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
89.Massa F, Marsicano G, Hermann H, Cannich A, Monory K, Cravatt BF, et al. The endogenous cannabinoid system protects against colonic inflammation. J Clin Invest. 2004;113:1202–9. doi: 10.1172/JCI200419465. [DOI] [PMC free article] [PubMed] [Google Scholar]
90.Alhouayek M, Lambert DM, Delzenne NM, Cani PD, Muccioli GG. Increasing endogenous 2-arachidonoylglycerol levels counteracts colitis and related systemic inflammation. FASEB J. 2011;25:2711–21. doi: 10.1096/fj.10-176602. [DOI] [PubMed] [Google Scholar]
91.Sałaga M, Mokrowiecka A, Zakrzewski PK, Cygankiewicz A, Leishman E, Sobczak M, et al. Experimental colitis in mice is attenuated by changes in the levels of endocannabinoid metabolites induced by selective inhibition of fatty acid amide hydrolase (FAAH) J Crohns Colitis. 2014;8:998–1009. doi: 10.1016/j.crohns.2014.01.025. [DOI] [PMC free article] [PubMed] [Google Scholar]
92.Sasso O, Migliore M, Habrant D, Armirotti A, Albani C, Summa M, et al. Multitarget fatty acid amide hydrolase/cyclooxygenase blockade suppresses intestinal inflammation and protects against nonsteroidal anti-inflammatory drug-dependent gastrointestinal damage. FASEB J. 2015;29:2616–27. doi: 10.1096/fj.15-270637. [DOI] [PMC free article] [PubMed] [Google Scholar]
93.Couch DG, Maudslay H, Doleman B, Lund JN, O’Sullivan SE. The use of cannabinoids in colitis: a systematic review and meta-analysis. Inflamm Bowel Dis. 2018;24:680–97. doi: 10.1093/ibd/izy014. [DOI] [PubMed] [Google Scholar]
94.Leinwand KL, Jones AA, Huang RH, Jedlicka P, Kao DJ, de Zoeten EF, et al. Cannabinoid receptor-2 ameliorates inflammation in murine model of Crohn’s Disease. J Crohns Colitis. 2017;11:1369–80. doi: 10.1093/ecco-jcc/jjx096. [DOI] [PMC free article] [PubMed] [Google Scholar]
95.Leinwand KL, Gerich ME, Hoffenberg EJ, Collins CB. Manipulation of the endocannabinoid system in colitis: a comprehensive review. Inflamm Bowel Dis. 2017;23:192–9. doi: 10.1097/MIB.0000000000001004. [DOI] [PMC free article] [PubMed] [Google Scholar]
96.Shamran H, Singh NP, Zumbrun EE, Murphy A, Taub DD, Mishra MK, et al. Fatty acid amide hydrolase (FAAH) blockade ameliorates experimental colitis by altering microRNA expression and suppressing inflammation. Brain Behav Immun. 2017;59:10–20. doi: 10.1016/j.bbi.2016.06.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
97.Zhao X, Liang P, Liu J, Jiang H, Fan X, Chen G, et al. Elevation of arachidonoylethanolamide levels by activation of the endocannabinoid system protects against colitis and ameliorates remote organ lesions in mice. Exp Ther Med. 2017;14:5664–70.. doi: 10.3892/etm.2017.5222. [DOI] [PMC free article] [PubMed] [Google Scholar]
98.Ahn K, Smith SE, Liimatta MB, Beidler D, Sadagopan N, Dudley DT, et al. Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain. J Pharm Exp Ther. 2011;338:114–24. doi: 10.1124/jpet.111.180257. [DOI] [PMC free article] [PubMed] [Google Scholar]
99.Johnson DS, Stiff C, Lazerwith SE, Kesten SR, Fay LK, Morris M, et al. Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor. ACS Med Chem Lett. 2011;2:91–96. doi: 10.1021/ml100190t. [DOI] [PMC free article] [PubMed] [Google Scholar]
100.Sticht MA, Lau DJ, Keenan CM, Cavin J-B, Morena M, Vemuri VK, et al. Endocannabinoid regulation of homeostatic feeding and stress-induced alterations in food intake in male rats. Br J Pharmacol. 2019;176:1524–40. doi: 10.1111/bph.14453. [DOI] [PMC free article] [PubMed] [Google Scholar]
101.DeVos SL, Miller TM. Direct intraventricular delivery of drugs to the rodent central nervous system. J Vis Exp. 2013;e50326. [DOI] [PMC free article] [PubMed]
102.Acharjee S, Verbeek M, Gomez CD, Bisht K, Lee B, Benoit L, et al. Reduced microglial activity and enhanced glutamate transmission in the basolateral amygdala in early CNS autoimmunity. J Neurosci. 2018;38:9019–33. doi: 10.1523/JNEUROSCI.0398-18.2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
103.Toriya M, Maekawa F, Maejima Y, Onaka T, Fujiwara K, Nakagawa T, et al. Long-term infusion of brain-derived neurotrophic factor reduces food intake and body weight via a corticotrophin-releasing hormone pathway in the paraventricular nucleus of the hypothalamus. J Neuroendocrinol. 2010;22:987–95. doi: 10.1111/j.1365-2826.2010.02039.x. [DOI] [PubMed] [Google Scholar]
104.Motulsky HJ, Brown RE. Detecting outliers when fitting data with nonlinear regression - a new method based on robust nonlinear regression and the false discovery rate. BMC Bioinforma. 2006;7:123. doi: 10.1186/1471-2105-7-123. [DOI] [PMC free article] [PubMed] [Google Scholar]
105.Calhoon GG, Tye KM. Resolving the neural circuits of anxiety. Nat Neurosci. 2015;18:1394–404. doi: 10.1038/nn.4101. [DOI] [PMC free article] [PubMed] [Google Scholar]
106.Gray JM, Wilson CD, Lee TTY, Pittman QJ, Deussing JM, Hillard CJ, et al. Sustained glucocorticoid exposure recruits cortico-limbic CRH signaling to modulate endocannabinoid function. Psychoneuroendocrinology. 2016;66:151–8. doi: 10.1016/j.psyneuen.2016.01.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
107.Cetinel S, Hancioğlu S, Sener E, Uner C, Kiliç M, Sener G, et al. Oxytocin treatment alleviates stress-aggravated colitis by a receptor-dependent mechanism. Regul Pept. 2010;160:146–52. doi: 10.1016/j.regpep.2009.11.011. [DOI] [PubMed] [Google Scholar]
108.Gadotti VM, Zamponi GW. Anxiolytic effects of the flavonoid luteolin in a mouse model of acute colitis. Mol Brain. 2019;12:114. doi: 10.1186/s13041-019-0539-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
109.Matisz CE, Vicentini FA, Hirota SA, Sharkey KA, Gruber AJ. Behavioral adaptations in a relapsing mouse model of colitis. Physiol Behav. 2020;216:112802. doi: 10.1016/j.physbeh.2020.112802. [DOI] [PubMed] [Google Scholar]
110.Patel S, Hill MN, Cheer JF, Wotjak CT, Holmes A. The endocannabinoid system as a target for novel anxiolytic drugs. Neurosci Biobehav Rev. 2017;76:56–66. doi: 10.1016/j.neubiorev.2016.12.033. [DOI] [PMC free article] [PubMed] [Google Scholar]
111.Flannery LE, Kerr DM, Finn DP, Roche M. FAAH inhibition attenuates TLR3-mediated hyperthermia, nociceptive- and anxiety-like behaviour in female rats. Behav Brain Res. 2018;353:11–20. doi: 10.1016/j.bbr.2018.06.030. [DOI] [PubMed] [Google Scholar]
112.Doenni VM, Gray JM, Song CM, Patel S, Hill MN, Pittman QJ. Deficient adolescent social behavior following early-life inflammation is ameliorated by augmentation of anandamide signaling. Brain Behav Immun. 2016;58:237–47. doi: 10.1016/j.bbi.2016.07.152. [DOI] [PMC free article] [PubMed] [Google Scholar]
113.Bedse G, Bluett RJ, Patrick TA, Romness NK, Gaulden AD, Kingsley PJ, et al. Therapeutic endocannabinoid augmentation for mood and anxiety disorders: comparative profiling of FAAH, MAGL and dual inhibitors. Transl Psychiatry. 2018;8:92. doi: 10.1038/s41398-018-0141-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
114.Dantzer R, Konsman JP, Bluthé RM, Kelley KW. Neural and humoral pathways of communication from the immune system to the brain: parallel or convergent? Auton Neurosci. 2000;85:60–65. doi: 10.1016/S1566-0702(00)00220-4. [DOI] [PubMed] [Google Scholar]
115.Taché Y, Bonaz B. Corticotropin-releasing factor receptors and stress-related alterations of gut motor function. J Clin Invest. 2007;117:33–40. doi: 10.1172/JCI30085. [DOI] [PMC free article] [PubMed] [Google Scholar]
116.Franchimont D, Bouma G, Galon J, Wolkersdörfer GW, Haidan A, Chrousos GP, et al. Adrenal cortical activation in murine colitis. Gastroenterology. 2000;119:1560–8. doi: 10.1053/gast.2000.20235. [DOI] [PubMed] [Google Scholar]
117.Deiteren A, Vermeulen W, Moreels TG, Pelckmans PA, De Man JG, De Winter BY. The effect of chemically induced colitis, psychological stress and their combination on visceral pain in female Wistar rats. Stress. 2014;17:431–44. doi: 10.3109/10253890.2014.951034. [DOI] [PubMed] [Google Scholar]
118.Parolaro D. Presence and functional regulation of cannabinoid receptors in immune cells. Life Sci. 1999;65:637–44. doi: 10.1016/S0024-3205(99)00286-6. [DOI] [PubMed] [Google Scholar]
119.Nagarkatti P, Pandey R, Rieder SA, Hegde VL, Nagarkatti M. Cannabinoids as novel anti-inflammatory drugs. Future Med Chem. 2009;1:1333–49. doi: 10.4155/fmc.09.93. [DOI] [PMC free article] [PubMed] [Google Scholar]
120.D’Argenio G, Valenti M, Scaglione G, Cosenza V, Sorrentini I, Di Marzo V. Up-regulation of anandamide levels as an endogenous mechanism and a pharmacological strategy to limit colon inflammation. FASEB J. 2006;20:568–70. doi: 10.1096/fj.05-4943fje. [DOI] [PubMed] [Google Scholar]
121.Storr MA, Keenan CM, Emmerdinger D, Zhang H, Yüce B, Sibaev A, et al. Targeting endocannabinoid degradation protects against experimental colitis in mice: involvement of CB1 and CB2 receptors. J Mol Med. 2008;86:925–36. doi: 10.1007/s00109-008-0359-6. [DOI] [PubMed] [Google Scholar]
122.Fichna J, Bawa M, Thakur GA, Tichkule R, Makriyannis A, McCafferty D-M, et al. Cannabinoids alleviate experimentally induced intestinal inflammation by acting at central and peripheral receptors. PLoS One. 2014;9:e109115. doi: 10.1371/journal.pone.0109115. [DOI] [PMC free article] [PubMed] [Google Scholar]
123.Busquets-Garcia A, Puighermanal E, Pastor A, de la Torre R, Maldonado R, Ozaita A. Differential role of anandamide and 2-arachidonoylglycerol in memory and anxiety-like responses. Biol Psychiatry. 2011;70:479–86. doi: 10.1016/j.biopsych.2011.04.022. [DOI] [PubMed] [Google Scholar]
124.Kinsey SG, O’Neal ST, Long JZ, Cravatt BF, Lichtman AH. Inhibition of endocannabinoid catabolic enzymes elicits anxiolytic-like effects in the marble burying assay. Pharm Biochem Behav. 2011;98:21–27. doi: 10.1016/j.pbb.2010.12.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
125.Sciolino NR, Zhou W, Hohmann AG. Enhancement of endocannabinoid signaling with JZL184, an inhibitor of the 2-arachidonoylglycerol hydrolyzing enzyme monoacylglycerol lipase, produces anxiolytic effects under conditions of high environmental aversiveness in rats. Pharm Res. 2011;64:226–34. doi: 10.1016/j.phrs.2011.04.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
126.Sumislawski JJ, Ramikie TS, Patel S. Reversible gating of endocannabinoid plasticity in the amygdala by chronic stress: a potential role for monoacylglycerol lipase inhibition in the prevention of stress-induced behavioral adaptation. Neuropsychopharmacology. 2011;36:2750–61. doi: 10.1038/npp.2011.166. [DOI] [PMC free article] [PubMed] [Google Scholar]
127.Hauer D, Schelling G, Gola H, Campolongo P, Morath J, Roozendaal B, et al. Plasma concentrations of endocannabinoids and related primary fatty acid amides in patients with post-traumatic stress disorder. PLoS One. 2013;8:e62741. doi: 10.1371/journal.pone.0062741. [DOI] [PMC free article] [PubMed] [Google Scholar]
128.Domi E, Uhrig S, Soverchia L, Spanagel R, Hansson AC, Barbier E, et al. Genetic deletion of neuronal PPARγ enhances the emotional response to acute stress and exacerbates anxiety: an effect reversed by rescue of amygdala PPARγ function. J Neurosci. 2016;36:12611–23. doi: 10.1523/JNEUROSCI.4127-15.2016. [DOI] [PMC free article] [PubMed] [Google Scholar]
129.Mirza R, Sharma B. Selective modulator of peroxisome proliferator-activated receptor-α protects propionic acid induced autism-like phenotypes in rats. Life Sci. 2018;214:106–17. doi: 10.1016/j.lfs.2018.10.045. [DOI] [PubMed] [Google Scholar]
130.Russo R, Cristiano C, Avagliano C, De Caro C, La Rana G, Raso GM, et al. Gut-brain axis: role of lipids in the regulation of inflammation, pain and CNS diseases. Curr Med Chem. 2018;25:3930–52. doi: 10.2174/0929867324666170216113756. [DOI] [PubMed] [Google Scholar]
131.De Gregorio D, Manchia M, Carpiniello B, Valtorta F, Nobile M, Gobbi G, et al. Role of palmitoylethanolamide (PEA) in depression: Translational evidence: Special Section on ‘Translational and Neuroscience Studies in Affective Disorders’. Section Editor, Maria Nobile MD, PhD. This Section of JAD focuses on the relevance of translational and neuroscience studies in providing a better understanding of the neural basis of affective disorders. The main aim is to briefly summaries relevant research findings in clinical neuroscience with particular regards to specific innovative topics in mood and anxiety disorders. J Affect Disord. 2019;255:S0165-0327(18)31599-4. doi: 10.1016/j.jad.2018.10.117. [DOI] [PubMed] [Google Scholar]
132.Zhao Q, Wang Q, Wang J, Tang M, Huang S, Peng K, et al. Maternal immune activation-induced PPARγ-dependent dysfunction of microglia associated with neurogenic impairment and aberrant postnatal behaviors in offspring. Neurobiol Dis. 2019;125:1–13. doi: 10.1016/j.nbd.2019.01.005. [DOI] [PubMed] [Google Scholar]
133.Christofides A, Konstantinidou E, Jani C, Boussiotis VA. The role of peroxisome proliferator-activated receptors (PPAR) in immune responses. Metabolism. 2021;114:154338. doi: 10.1016/j.metabol.2020.154338. [DOI] [PMC free article] [PubMed] [Google Scholar]
134.D’Souza DC, Cortes-Briones J, Creatura G, Bluez G, Thurnauer H, Deaso E, et al. Efficacy and safety of a fatty acid amide hydrolase inhibitor (PF-04457845) in the treatment of cannabis withdrawal and dependence in men: a double-blind, placebo-controlled, parallel group, phase 2a single-site randomised controlled trial. Lancet Psychiatry. 2019;6:35–45. doi: 10.1016/S2215-0366(18)30427-9. [DOI] [PubMed] [Google Scholar]
135.Asratian A, Lindé J, Morena M, Haataja R, Hammar V. Elevated Anandamide, Enhanced Recall of Fear Extinction, and Attenuated Stress Responses Following Inhibition of Fatty Acid Amide Hydrolase: A Randomized, Controlled Experimental Medicine Trial. Biol Psychiatry. 2020;87:538–47. doi: 10.1016/j.biopsych.2019.07.034. [DOI] [PubMed] [Google Scholar]
136.Schmidt ME, Liebowitz MR, Stein MB, Grunfeld J, Van Hove I, Simmons WK, et al. The effects of inhibition of fatty acid amide hydrolase (FAAH) by JNJ-42165279 in social anxiety disorder: a double-blind, randomized, placebo-controlled proof-of-concept study. Neuropsychopharmacology. 2020. 10.1038/s41386-020-00888-1. [DOI] [PMC free article] [PubMed]
137.Fitzgibbon M, Finn DP, Roche M. High times for painful blues: the endocannabinoid system in pain-depression comorbidity. Int J Neuropsychopharmacol. 2015;19:pyv095. doi: 10.1093/ijnp/pyv095. [DOI] [PMC free article] [PubMed] [Google Scholar]
138.Doeve BH, van de Meeberg MM, van Schaik FDM, Fidder HH A systematic review with meta-analysis of the efficacy of cannabis and cannabinoids for inflammatory bowel disease: what can we learn from randomized and nonrandomized studies? J Clin Gastroenterol. 2020. 10.1097/MCG.0000000000001393. [DOI] [PubMed]

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[CR1] 1.Marrie RA, Walld R, Bolton JM, Sareen J, Patten SB, Singer A, et al. Psychiatric comorbidity increases mortality in immune-mediated inflammatory diseases. Gen Hosp Psychiatry. 2018;53:65–72. doi: 10.1016/j.genhosppsych.2018.06.001. [DOI] [PubMed] [Google Scholar]

[CR2] 2.Bernstein CN, Hitchon CA, Walld R, Bolton JM, Sareen J, Walker JR, et al. Increased burden of psychiatric disorders in inflammatory bowel disease. Inflamm Bowel Dis. 2019;25:360–8. doi: 10.1093/ibd/izy235. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR3] 3.Moulton CD, Pavlidis P, Norton C, Norton S, Pariante C, Hayee B, et al. Depressive symptoms in inflammatory bowel disease: an extraintestinal manifestation of inflammation? Clin Exp Immunol. 2019;197:308–18. doi: 10.1111/cei.13276. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR4] 4.Whitehouse CE, Fisk JD, Bernstein CN, Berrigan LI, Bolton JM, Graff LA, et al. Comorbid anxiety, depression, and cognition in MS and other immune-mediated disorders. Neurology. 2019;92:e406–17. doi: 10.1212/WNL.0000000000006854. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR5] 5.Thomann AK, Mak JWY, Zhang JW, Wuestenberg T, Ebert MP, Sung JJY, et al. Review article: bugs, inflammation and mood-a microbiota-based approach to psychiatric symptoms in inflammatory bowel diseases. Aliment Pharm Ther. 2020;52:247–66. doi: 10.1111/apt.15787. [DOI] [PubMed] [Google Scholar]

[CR6] 6.Gracie DJ, Irvine AJ, Sood R, Mikocka-Walus A, Hamlin PJ, Ford AC. Effect of psychological therapy on disease activity, psychological comorbidity, and quality of life in inflammatory bowel disease: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2017;2:189–99. doi: 10.1016/S2468-1253(16)30206-0. [DOI] [PubMed] [Google Scholar]

[CR7] 7.Jones JL, Nguyen GC, Benchimol EI, Bernstein CN, Bitton A, Kaplan GG, et al. The impact of inflammatory bowel disease in Canada 2018: quality of life. J Can Assoc Gastroenterol. 2019;2:S42–S48.. doi: 10.1093/jcag/gwy048. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR8] 8.Porcelli P, Leoci C, Guerra V. A prospective study of the relationship between disease activity and psychologic distress in patients with inflammatory bowel disease. Scand J Gastroenterol. 1996;31:792–6. doi: 10.3109/00365529609010354. [DOI] [PubMed] [Google Scholar]

[CR9] 9.Addolorato G, Capristo E, Stefanini GF, Gasbarrini G. Inflammatory bowel disease: a study of the association between anxiety and depression, physical morbidity, and nutritional status. Scand J Gastroenterol. 1997;32:1013–21. doi: 10.3109/00365529709011218. [DOI] [PubMed] [Google Scholar]

[CR10] 10.Fuller-Thomson E, Sulman J. Depression and inflammatory bowel disease: findings from two nationally representative Canadian surveys. Inflamm Bowel Dis. 2006;12:697–707. doi: 10.1097/00054725-200608000-00005. [DOI] [PubMed] [Google Scholar]

[CR11] 11.Kovács Z, Kovács F. Depressive and anxiety symptoms, dysfunctional attitudes and social aspects in irritable bowel syndrome and inflammatory bowel disease. Int J Psychiatry Med. 2007;37:245–55. doi: 10.2190/PM.37.3.a. [DOI] [PubMed] [Google Scholar]

[CR12] 12.Lerebours E, Gower-Rousseau C, Merle V, Brazier F, Debeugny S, Marti R, et al. Stressful life events as a risk factor for inflammatory bowel disease onset: a population-based case-control study. Am J Gastroenterol. 2007;102:122–31. doi: 10.1111/j.1572-0241.2006.00931.x. [DOI] [PubMed] [Google Scholar]

[CR13] 13.Walker JR, Ediger JP, Graff LA, Greenfeld JM, Clara I, Lix L, et al. The Manitoba IBD cohort study: a population-based study of the prevalence of lifetime and 12-month anxiety and mood disorders. Am J Gastroenterol. 2008;103:1989–97. doi: 10.1111/j.1572-0241.2008.01980.x. [DOI] [PubMed] [Google Scholar]

[CR14] 14.Hyphantis TN, Tomenson B, Bai M, Tsianos E, Mavreas V, Creed F. Psychological distress, somatization, and defense mechanisms associated with quality of life in inflammatory bowel disease patients. Dig Dis Sci. 2010;55:724–32. doi: 10.1007/s10620-009-0762-z. [DOI] [PubMed] [Google Scholar]

[CR15] 15.Filipovic BR, Filipovic BF. Psychiatric comorbidity in the treatment of patients with inflammatory bowel disease. World J Gastroenterol. 2014;20:3552–63. doi: 10.3748/wjg.v20.i13.3552. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR16] 16.Tribbick D, Salzberg M, Ftanou M, Connell WR, Macrae F, Kamm MA, et al. Prevalence of mental health disorders in inflammatory bowel disease: an Australian outpatient cohort. Clin Exp Gastroenterol. 2015;8:197–204. doi: 10.2147/CEG.S77567. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR17] 17.Fuller-Thomson E, Lateef R, Sulman J. Robust association between inflammatory bowel disease and generalized anxiety disorder: findings from a nationally representative Canadian Study. Inflamm Bowel Dis. 2015;21:2341–8. doi: 10.1097/MIB.0000000000000551. [DOI] [PubMed] [Google Scholar]

[CR18] 18.Fiest KM, Bernstein CN, Walker JR, Graff LA, Hitchon CA, Peschken CA, et al. Systematic review of interventions for depression and anxiety in persons with inflammatory bowel disease. BMC Res Notes. 2016;9:404. doi: 10.1186/s13104-016-2204-2. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR19] 19.Mikocka-Walus A, Knowles SR, Keefer L, Graff L. Controversies revisited: a systematic review of the comorbidity of depression and anxiety with inflammatory bowel diseases. Inflamm Bowel Dis. 2016;22:752–62. doi: 10.1097/MIB.0000000000000620. [DOI] [PubMed] [Google Scholar]

[CR20] 20.Neuendorf R, Harding A, Stello N, Hanes D, Wahbeh H. Depression and anxiety in patients with inflammatory bowel disease: a systematic review. J Psychosom Res. 2016;87:70–80. doi: 10.1016/j.jpsychores.2016.06.001. [DOI] [PubMed] [Google Scholar]

[CR21] 21.Byrne G, Rosenfeld G, Leung Y, Qian H, Raudzus J, Nunez C, et al. Prevalence of anxiety and depression in patients with inflammatory bowel disease. Can J Gastroenterol Hepatol. 2017;2017:6496727. doi: 10.1155/2017/6496727. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR22] 22.Marrie RA, Walld R, Bolton JM, Sareen J, Walker JR, Patten SB, et al. Increased incidence of psychiatric disorders in immune-mediated inflammatory disease. J Psychosom Res. 2017;101:17–23. doi: 10.1016/j.jpsychores.2017.07.015. [DOI] [PubMed] [Google Scholar]

[CR23] 23.Regueiro M, Greer JB, Szigethy E. Etiology and treatment of pain and psychosocial issues in patients with inflammatory bowel diseases. Gastroenterology. 2017;152:430–9.e4. doi: 10.1053/j.gastro.2016.10.036. [DOI] [PubMed] [Google Scholar]

[CR24] 24.Bhamre R, Sawrav S, Adarkar S, Sakaria RJ, Bhatia S. Psychiatric comorbidities in patients with inflammatory bowel disease. Indian J Gastroenterol. 2018;37:307–12. doi: 10.1007/s12664-018-0870-9. [DOI] [PubMed] [Google Scholar]

[CR25] 25.Navabi S, Gorrepati VS, Yadav S, Chintanaboina J, Maher S, Demuth P, et al. Influences and impact of anxiety and depression in the setting of inflammatory bowel disease. Inflamm Bowel Dis. 2018;24:2303–8. doi: 10.1093/ibd/izy143. [DOI] [PubMed] [Google Scholar]

[CR26] 26.Choi K, Chun J, Han K, Park S, Soh H, Kim J, et al. Risk of anxiety and depression in patients with inflammatory bowel disease: a nationwide, population-based study. J Clin Med. 2019;8:654. doi: 10.3390/jcm8050654. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR27] 27.Lewis K, Marrie RA, Bernstein CN, Graff LA, Patten SB, Sareen J, et al. The prevalence and risk factors of undiagnosed depression and anxiety disorders among patients with inflammatory bowel disease. Inflamm Bowel Dis. 2019;25:1674–80. doi: 10.1093/ibd/izz045. [DOI] [PubMed] [Google Scholar]

[CR28] 28.Narula N, Pinto-Sanchez MI, Calo NC, Ford AC, Bercik P, Reinisch W, et al. Anxiety but not depression predicts poor outcomes in inflammatory bowel disease. Inflamm Bowel Dis. 2019;25:1255–61. doi: 10.1093/ibd/izy385. [DOI] [PubMed] [Google Scholar]

[CR29] 29.Thakur ER, Sansgiry S, Kramer JR, Waljee AK, Gaidos JK, Feagins LA, et al. The incidence and prevalence of anxiety, depression, and post-traumatic stress disorder in a national cohort of US Veterans With Inflammatory Bowel Disease. Inflamm Bowel Dis. 2020;26:1423–8. doi: 10.1093/ibd/izz280. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR30] 30.Walker EA, Gelfand AN, Gelfand MD, Katon WJ. Psychiatric diagnoses, sexual and physical victimization, and disability in patients with irritable bowel syndrome or inflammatory bowel disease. Psychol Med. 1995;25:1259–67. doi: 10.1017/S0033291700033225. [DOI] [PubMed] [Google Scholar]

[CR31] 31.Sewitch MJ, Abrahamowicz M, Bitton A, Daly D, Wild GE, Cohen A, et al. Psychological distress, social support, and disease activity in patients with inflammatory bowel disease. Am J Gastroenterol. 2001;96:1470–9. doi: 10.1111/j.1572-0241.2001.03800.x. [DOI] [PubMed] [Google Scholar]

[CR32] 32.Guthrie E, Jackson J, Shaffer J, Thompson D, Tomenson B, Creed F. Psychological disorder and severity of inflammatory bowel disease predict health-related quality of life in ulcerative colitis and Crohn’s disease. Am J Gastroenterol. 2002;97:1994–9. doi: 10.1111/j.1572-0241.2002.05842.x. [DOI] [PubMed] [Google Scholar]

[CR33] 33.Casellas F, Arenas JI, Baudet JS, Fábregas S, García N, Gelabert J, et al. Impairment of health-related quality of life in patients with inflammatory bowel disease: a Spanish multicenter study. Inflamm Bowel Dis. 2005;11:488–96. doi: 10.1097/01.MIB.0000159661.55028.56. [DOI] [PubMed] [Google Scholar]

[CR34] 34.Graff LA, Walker JR, Lix L, Clara I, Rawsthorne P, Rogala L, et al. The relationship of inflammatory bowel disease type and activity to psychological functioning and quality of life. Clin Gastroenterol Hepatol. 2006;4:1491–501. doi: 10.1016/j.cgh.2006.09.027. [DOI] [PubMed] [Google Scholar]

[CR35] 35.Bonaz BL, Bernstein CN. Brain-gut interactions in inflammatory bowel disease. Gastroenterology. 2013;144:36–49. doi: 10.1053/j.gastro.2012.10.003. [DOI] [PubMed] [Google Scholar]

[CR36] 36.Mulak A, Bonaz B. Irritable bowel syndrome: a model of the brain-gut interactions. Med Sci Monit. 2004;10:RA55–62. [PubMed] [Google Scholar]

[CR37] 37.Reber SO. Stress and animal models of inflammatory bowel disease–an update on the role of the hypothalamo-pituitary-adrenal axis. Psychoneuroendocrinology. 2012;37:1–19. doi: 10.1016/j.psyneuen.2011.05.014. [DOI] [PubMed] [Google Scholar]

[CR38] 38.Sharkey KA, Wiley JW. The role of the endocannabinoid system in the brain-gut axis. Gastroenterology. 2016;151:252–66. doi: 10.1053/j.gastro.2016.04.015. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR39] 39.Nestler EJ, Barrot M, DiLeone RJ, Eisch AJ, Gold SJ, Monteggia LM. Neurobiology of depression. Neuron. 2002;34:13–25. doi: 10.1016/S0896-6273(02)00653-0. [DOI] [PubMed] [Google Scholar]

[CR40] 40.Tafet GE, Nemeroff CB. The links between stress and depression: psychoneuroendocrinological, genetic, and environmental interactions. J Neuropsychiatry Clin Neurosci. 2016;28:77–88. doi: 10.1176/appi.neuropsych.15030053. [DOI] [PubMed] [Google Scholar]

[CR41] 41.Hill MN, McEwen BS. Involvement of the endocannabinoid system in the neurobehavioural effects of stress and glucocorticoids. Prog Neuropsychopharmacol Biol Psychiatry. 2010;34:791–7. doi: 10.1016/j.pnpbp.2009.11.001. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR42] 42.Hill MN, Tasker JG. Endocannabinoid signaling, glucocorticoid-mediated negative feedback, and regulation of the hypothalamic-pituitary-adrenal axis. Neuroscience. 2012;204:5–16. doi: 10.1016/j.neuroscience.2011.12.030. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR43] 43.Morena M, Patel S, Bains JS, Hill MN. Neurobiological Interactions Between Stress and the Endocannabinoid System. Neuropsychopharmacology. 2016;41:80–102. doi: 10.1038/npp.2015.166. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR44] 44.Haller J, Bakos N, Szirmay M, Ledent C, Freund TF. The effects of genetic and pharmacological blockade of the CB1 cannabinoid receptor on anxiety. Eur J Neurosci. 2002;16:1395–8. doi: 10.1046/j.1460-9568.2002.02192.x. [DOI] [PubMed] [Google Scholar]

[CR45] 45.Haller J, Varga B, Ledent C, Freund TF. CB1 cannabinoid receptors mediate anxiolytic effects: convergent genetic and pharmacological evidence with CB1-specific agents. Behav Pharmacol. 2004;15:299–304. doi: 10.1097/01.fbp.0000135704.56422.40. [DOI] [PubMed] [Google Scholar]

[CR46] 46.Hill MN, Hillard CJ, McEwen BS. Alterations in corticolimbic dendritic morphology and emotional behavior in cannabinoid CB1 receptor-deficient mice parallel the effects of chronic stress. Cereb Cortex. 2011;21:2056–64. doi: 10.1093/cercor/bhq280. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR47] 47.Patel S, Cravatt BF, Hillard CJ. Synergistic interactions between cannabinoids and environmental stress in the activation of the central amygdala. Neuropsychopharmacology. 2005;30:497–507. doi: 10.1038/sj.npp.1300535. [DOI] [PubMed] [Google Scholar]

[CR48] 48.Hill MN, McLaughlin RJ, Morrish AC, Viau V, Floresco SB, Hillard CJ, et al. Suppression of amygdalar endocannabinoid signaling by stress contributes to activation of the hypothalamic-pituitary-adrenal axis. Neuropsychopharmacology. 2009;34:2733–45. doi: 10.1038/npp.2009.114. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR49] 49.Hill MN, Kumar SA, Filipski SB, Iverson M, Stuhr KL, Keith JM, et al. Disruption of fatty acid amide hydrolase activity prevents the effects of chronic stress on anxiety and amygdalar microstructure. Mol Psychiatry. 2013;18:1125–35. doi: 10.1038/mp.2012.90. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR50] 50.Gray JM, Vecchiarelli HA, Morena M, Lee TTY, Hermanson DJ, Kim AB, et al. Corticotropin-releasing hormone drives anandamide hydrolysis in the amygdala to promote anxiety. J Neurosci. 2015;35:3879–92. doi: 10.1523/JNEUROSCI.2737-14.2015. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR51] 51.Rubino T, Realini N, Castiglioni C, Guidali C, Viganó D, Marras E, et al. Role in anxiety behavior of the endocannabinoid system in the prefrontal cortex. Cereb Cortex. 2008;18:1292–301. doi: 10.1093/cercor/bhm161. [DOI] [PubMed] [Google Scholar]

[CR52] 52.Campos AC, Brant F, Miranda AS, Machado FS, Teixeira AL. Cannabidiol increases survival and promotes rescue of cognitive function in a murine model of cerebral malaria. Neuroscience. 2015;289:166–80. doi: 10.1016/j.neuroscience.2014.12.051. [DOI] [PubMed] [Google Scholar]

[CR53] 53.de la Tremblaye PB, Benoit SM, Schock S, Plamondon H. CRHR1 exacerbates the glial inflammatory response and alters BDNF/TrkB/pCREB signaling in a rat model of global cerebral ischemia: implications for neuroprotection and cognitive recovery. Prog Neuropsychopharmacol Biol Psychiatry. 2017;79:234–48. doi: 10.1016/j.pnpbp.2017.06.021. [DOI] [PubMed] [Google Scholar]

[CR54] 54.Ji G, Fu Y, Ruppert KA, Neugebauer V. Pain-related anxiety-like behavior requires CRF1 receptors in the amygdala. Mol Pain. 2007;3:13. doi: 10.1186/1744-8069-3-13. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR55] 55.Fu Y, Neugebauer V. Differential mechanisms of CRF1 and CRF2 receptor functions in the amygdala in pain-related synaptic facilitation and behavior. J Neurosci. 2008;28:3861–76. doi: 10.1523/JNEUROSCI.0227-08.2008. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR56] 56.O’Malley D, Quigley EMM, Dinan TG, Cryan JF. Do interactions between stress and immune responses lead to symptom exacerbations in irritable bowel syndrome? Brain Behav Immun. 2011;25:1333–41. doi: 10.1016/j.bbi.2011.04.009. [DOI] [PubMed] [Google Scholar]

[CR57] 57.Taché Y. Corticotrophin-releasing factor 1 activation in the central amygdale and visceral hyperalgesia. Neurogastroenterol Motil. 2015;27:1–6. doi: 10.1111/nmo.12495. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR58] 58.Schäfer M, Mousa SA, Stein C. Corticotropin-releasing factor in antinociception and inflammation. Eur J Pharmacol. 1997;323:1–10. doi: 10.1016/S0014-2999(97)00057-5. [DOI] [PubMed] [Google Scholar]

[CR59] 59.Bravo JA, Dinan TG, Cryan JF. Alterations in the central CRF system of two different rat models of comorbid depression and functional gastrointestinal disorders. Int J Neuropsychopharmacol. 2011;14:666–83. doi: 10.1017/S1461145710000994. [DOI] [PubMed] [Google Scholar]

[CR60] 60.Hubbard CS, Labus JS, Bueller J, Stains J, Suyenobu B, Dukes GE, et al. Corticotropin-releasing factor receptor 1 antagonist alters regional activation and effective connectivity in an emotional-arousal circuit during expectation of abdominal pain. J Neurosci. 2011;31:12491–500. doi: 10.1523/JNEUROSCI.1860-11.2011. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR61] 61.Labus JS, Hubbard CS, Bueller J, Ebrat B, Tillisch K, Chen M, et al. Impaired emotional learning and involvement of the corticotropin-releasing factor signaling system in patients with irritable bowel syndrome. Gastroenterology. 2013;145:1253–61.e1-3. doi: 10.1053/j.gastro.2013.08.016. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR62] 62.Neurath M, Fuss I, Strober W. TNBS-colitis. Int Rev Immunol. 2000;19:51–62. doi: 10.3109/08830180009048389. [DOI] [PubMed] [Google Scholar]

[CR63] 63.Chassaing B, Aitken JD, Malleshappa M, Vijay-Kumar M. Dextran sulfate sodium (DSS)-induced colitis in mice. Curr Protoc Immunol. 2014;104:15.25.1–15.25.14. doi: 10.1002/0471142735.im1525s104. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR64] 64.Kiesler P, Fuss IJ, Strober W. Experimental models of inflammatory bowel diseases. Cell Mol Gastroenterol Hepatol. 2015;1:154–70. doi: 10.1016/j.jcmgh.2015.01.006. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR65] 65.Antoniou E, Margonis GA, Angelou A, Pikouli A, Argiri P, Karavokyros I, et al. The TNBS-induced colitis animal model: An overview. Ann Med Surg. 2016;11:9–15. doi: 10.1016/j.amsu.2016.07.019. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR66] 66.Kresse AE, Million M, Saperas E, Taché Y. Colitis induces CRF expression in hypothalamic magnocellular neurons and blunts CRF gene response to stress in rats. Am J Physiol Gastrointest Liver Physiol. 2001;281:G1203–1213. doi: 10.1152/ajpgi.2001.281.5.G1203. [DOI] [PubMed] [Google Scholar]

[CR67] 67.Kojima K, Naruse Y, Iijima N, Wakabayashi N, Mitsufuji S, Ibata Y, et al. HPA-axis responses during experimental colitis in the rat. Am J Physiol Regul Integr Comp Physiol. 2002;282:R1348–1355. doi: 10.1152/ajpregu.00260.2001. [DOI] [PubMed] [Google Scholar]

[CR68] 68.Porcher C, Sinniger V, Juhem A, Mouchet P, Bonaz B. Neuronal activity and CRF receptor gene transcription in the brains of rats with colitis. Am J Physiol Gastrointest Liver Physiol. 2004;287:G803–814. doi: 10.1152/ajpgi.00135.2004. [DOI] [PubMed] [Google Scholar]

[CR69] 69.Greenwood-Van Meerveld B, Johnson AC, Schulkin J, Myers DA. Long-term expression of corticotropin-releasing factor (CRF) in the paraventricular nucleus of the hypothalamus in response to an acute colonic inflammation. Brain Res. 2006;1071:91–96. doi: 10.1016/j.brainres.2005.11.071. [DOI] [PubMed] [Google Scholar]

[CR70] 70.Lyte M, Li W, Opitz N, Gaykema RPA, Goehler LE. Induction of anxiety-like behavior in mice during the initial stages of infection with the agent of murine colonic hyperplasia citrobacter rodentium. Physiol Behav. 2006;89:350–7. doi: 10.1016/j.physbeh.2006.06.019. [DOI] [PubMed] [Google Scholar]

[CR71] 71.Bercik P, Verdu EF, Foster JA, Macri J, Potter M, Huang X, et al. Chronic gastrointestinal inflammation induces anxiety-like behavior and alters central nervous system biochemistry in mice. Gastroenterology. 2010;139:2102–12.e1. doi: 10.1053/j.gastro.2010.06.063. [DOI] [PubMed] [Google Scholar]

[CR72] 72.Chen J, Winston JH, Fu Y, Guptarak J, Jensen KL, Shi X-Z, et al. Genesis of anxiety, depression, and ongoing abdominal discomfort in ulcerative colitis-like colon inflammation. Am J Physiol Regul Integr Comp Physiol. 2015;308:R18–27. doi: 10.1152/ajpregu.00298.2014. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR73] 73.Nyuyki KD, Cluny NL, Swain MG, Sharkey KA, Pittman QJ. Altered brain excitability and increased anxiety in mice with experimental colitis: consideration of hyperalgesia and sex differences. Front Behav Neurosci. 2018;12:58. doi: 10.3389/fnbeh.2018.00058. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR74] 74.McCafferty DM, Sharkey KA, Wallace JL. Beneficial effects of local or systemic lidocaine in experimental colitis. Am J Physiol. 1994;266:G560–567. doi: 10.1152/ajpgi.1994.266.4.G560. [DOI] [PubMed] [Google Scholar]

[CR75] 75.Natah SS, Mouihate A, Pittman QJ, Sharkey KA. Disruption of the blood-brain barrier during TNBS colitis. Neurogastroenterol Motil. 2005;17:433–46. doi: 10.1111/j.1365-2982.2005.00654.x. [DOI] [PubMed] [Google Scholar]

[CR76] 76.Spencer SJ, Hyland NP, Sharkey KA, Pittman QJ. Neonatal immune challenge exacerbates experimental colitis in adult rats: potential role for TNF-alpha. Am J Physiol Regul Integr Comp Physiol. 2007;292:R308–315. doi: 10.1152/ajpregu.00398.2006. [DOI] [PubMed] [Google Scholar]

[CR77] 77.Riazi K, Galic MA, Kuzmiski JB, Ho W, Sharkey KA, Pittman QJ. Microglial activation and TNFalpha production mediate altered CNS excitability following peripheral inflammation. Proc Natl Acad Sci USA. 2008;105:17151–6. doi: 10.1073/pnas.0806682105. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR78] 78.da Silva MS, Sánchez-Fidalgo S, Talero E, Cárdeno A, da Silva MA, Villegas W, et al. Anti-inflammatory intestinal activity of Abarema cochliacarpos (Gomes) Barneby & Grimes in TNBS colitis model. J Ethnopharmacol. 2010;128:467–75. doi: 10.1016/j.jep.2010.01.024. [DOI] [PubMed] [Google Scholar]

[CR79] 79.Ikeda M, Takeshima F, Isomoto H, Shikuwa S, Mizuta Y, Ozono Y, et al. Simvastatin attenuates trinitrobenzene sulfonic acid-induced colitis, but not oxazalone-induced colitis. Dig Dis Sci. 2008;53:1869–75. doi: 10.1007/s10620-007-0102-0. [DOI] [PubMed] [Google Scholar]

[CR80] 80.Takagi T, Naito Y, Mizushima K, Akagiri S, Suzuki T, Hirata I, et al. Inhalation of carbon monoxide ameliorates TNBS-induced colitis in mice through the inhibition of TNF-α expression. Dig Dis Sci. 2010;55:2797–804. doi: 10.1007/s10620-009-1112-x. [DOI] [PubMed] [Google Scholar]

[CR81] 81.Cluny NL, Keenan CM, Duncan M, Fox A, Lutz B, Sharkey KA. Naphthalen-1-yl-(4-pentyloxynaphthalen-1-yl)methanone (SAB378), a peripherally restricted cannabinoid CB1/CB2 receptor agonist, inhibits gastrointestinal motility but has no effect on experimental colitis in mice. J Pharm Exp Ther. 2010;334:973–80. doi: 10.1124/jpet.110.169946. [DOI] [PubMed] [Google Scholar]

[CR82] 82.Morena M, Aukema RJ, Leitl KD, Rashid AJ, Vecchiarelli HA, Josselyn SA, et al. Upregulation of anandamide hydrolysis in the basolateral complex of amygdala reduces fear memory expression and indices of stress and anxiety. J Neurosci. 2019;39:1275–92. doi: 10.1523/JNEUROSCI.2251-18.2018. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR83] 83.Vecchiarelli HA, Gandhi CP, Gray JM, Morena M, Hassan KI, Hill MN. Divergent responses of inflammatory mediators within the amygdala and medial prefrontal cortex to acute psychological stress. Brain Behav Immun. 2016;51:70–91. doi: 10.1016/j.bbi.2015.07.026. [DOI] [PubMed] [Google Scholar]

[CR84] 84.Vecchiarelli HA, Gandhi CP, Hill MN. Acute psychological stress modulates the expression of enzymes involved in the kynurenine pathway throughout corticolimbic circuits in adult male rats. Neural Plast. 2016;2016:7215684. doi: 10.1155/2016/7215684. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR85] 85.Hill MN, Karatsoreos IN, Hillard CJ, McEwen BS. Rapid elevations in limbic endocannabinoid content by glucocorticoid hormones in vivo. Psychoneuroendocrinology. 2010;35:1333–8. doi: 10.1016/j.psyneuen.2010.03.005. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR86] 86.Qi M, Morena M, Vecchiarelli HA, Hill MN, Schriemer DC. A robust capillary liquid chromatography/tandem mass spectrometry method for quantitation of neuromodulatory endocannabinoids. Rapid Commun Mass Spectrom. 2015;29:1889–97. doi: 10.1002/rcm.7277. [DOI] [PubMed] [Google Scholar]

[CR87] 87.Atsak P, Morena M, Schoenmaker C, Tabak E, Oomen CA, Jamil S, et al. Glucocorticoid-endocannabinoid uncoupling mediates fear suppression deficits after early - Life stress. Psychoneuroendocrinology. 2018;91:41–49. doi: 10.1016/j.psyneuen.2018.02.021. [DOI] [PubMed] [Google Scholar]

[CR88] 88.Berger AL, Henricks AM, Lugo JM, Wright HR, Warrick CR, Sticht MA, et al. The lateral habenula directs coping styles under conditions of stress via recruitment of the endocannabinoid system. Biol Psychiatry. 2018;84:611–23. doi: 10.1016/j.biopsych.2018.04.018. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR89] 89.Massa F, Marsicano G, Hermann H, Cannich A, Monory K, Cravatt BF, et al. The endogenous cannabinoid system protects against colonic inflammation. J Clin Invest. 2004;113:1202–9. doi: 10.1172/JCI200419465. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR90] 90.Alhouayek M, Lambert DM, Delzenne NM, Cani PD, Muccioli GG. Increasing endogenous 2-arachidonoylglycerol levels counteracts colitis and related systemic inflammation. FASEB J. 2011;25:2711–21. doi: 10.1096/fj.10-176602. [DOI] [PubMed] [Google Scholar]

[CR91] 91.Sałaga M, Mokrowiecka A, Zakrzewski PK, Cygankiewicz A, Leishman E, Sobczak M, et al. Experimental colitis in mice is attenuated by changes in the levels of endocannabinoid metabolites induced by selective inhibition of fatty acid amide hydrolase (FAAH) J Crohns Colitis. 2014;8:998–1009. doi: 10.1016/j.crohns.2014.01.025. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR92] 92.Sasso O, Migliore M, Habrant D, Armirotti A, Albani C, Summa M, et al. Multitarget fatty acid amide hydrolase/cyclooxygenase blockade suppresses intestinal inflammation and protects against nonsteroidal anti-inflammatory drug-dependent gastrointestinal damage. FASEB J. 2015;29:2616–27. doi: 10.1096/fj.15-270637. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR93] 93.Couch DG, Maudslay H, Doleman B, Lund JN, O’Sullivan SE. The use of cannabinoids in colitis: a systematic review and meta-analysis. Inflamm Bowel Dis. 2018;24:680–97. doi: 10.1093/ibd/izy014. [DOI] [PubMed] [Google Scholar]

[CR94] 94.Leinwand KL, Jones AA, Huang RH, Jedlicka P, Kao DJ, de Zoeten EF, et al. Cannabinoid receptor-2 ameliorates inflammation in murine model of Crohn’s Disease. J Crohns Colitis. 2017;11:1369–80. doi: 10.1093/ecco-jcc/jjx096. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR95] 95.Leinwand KL, Gerich ME, Hoffenberg EJ, Collins CB. Manipulation of the endocannabinoid system in colitis: a comprehensive review. Inflamm Bowel Dis. 2017;23:192–9. doi: 10.1097/MIB.0000000000001004. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR96] 96.Shamran H, Singh NP, Zumbrun EE, Murphy A, Taub DD, Mishra MK, et al. Fatty acid amide hydrolase (FAAH) blockade ameliorates experimental colitis by altering microRNA expression and suppressing inflammation. Brain Behav Immun. 2017;59:10–20. doi: 10.1016/j.bbi.2016.06.008. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR97] 97.Zhao X, Liang P, Liu J, Jiang H, Fan X, Chen G, et al. Elevation of arachidonoylethanolamide levels by activation of the endocannabinoid system protects against colitis and ameliorates remote organ lesions in mice. Exp Ther Med. 2017;14:5664–70.. doi: 10.3892/etm.2017.5222. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR98] 98.Ahn K, Smith SE, Liimatta MB, Beidler D, Sadagopan N, Dudley DT, et al. Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain. J Pharm Exp Ther. 2011;338:114–24. doi: 10.1124/jpet.111.180257. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR99] 99.Johnson DS, Stiff C, Lazerwith SE, Kesten SR, Fay LK, Morris M, et al. Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor. ACS Med Chem Lett. 2011;2:91–96. doi: 10.1021/ml100190t. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR100] 100.Sticht MA, Lau DJ, Keenan CM, Cavin J-B, Morena M, Vemuri VK, et al. Endocannabinoid regulation of homeostatic feeding and stress-induced alterations in food intake in male rats. Br J Pharmacol. 2019;176:1524–40. doi: 10.1111/bph.14453. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR101] 101.DeVos SL, Miller TM. Direct intraventricular delivery of drugs to the rodent central nervous system. J Vis Exp. 2013;e50326. [DOI] [PMC free article] [PubMed]

[CR102] 102.Acharjee S, Verbeek M, Gomez CD, Bisht K, Lee B, Benoit L, et al. Reduced microglial activity and enhanced glutamate transmission in the basolateral amygdala in early CNS autoimmunity. J Neurosci. 2018;38:9019–33. doi: 10.1523/JNEUROSCI.0398-18.2018. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR103] 103.Toriya M, Maekawa F, Maejima Y, Onaka T, Fujiwara K, Nakagawa T, et al. Long-term infusion of brain-derived neurotrophic factor reduces food intake and body weight via a corticotrophin-releasing hormone pathway in the paraventricular nucleus of the hypothalamus. J Neuroendocrinol. 2010;22:987–95. doi: 10.1111/j.1365-2826.2010.02039.x. [DOI] [PubMed] [Google Scholar]

[CR104] 104.Motulsky HJ, Brown RE. Detecting outliers when fitting data with nonlinear regression - a new method based on robust nonlinear regression and the false discovery rate. BMC Bioinforma. 2006;7:123. doi: 10.1186/1471-2105-7-123. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR105] 105.Calhoon GG, Tye KM. Resolving the neural circuits of anxiety. Nat Neurosci. 2015;18:1394–404. doi: 10.1038/nn.4101. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR106] 106.Gray JM, Wilson CD, Lee TTY, Pittman QJ, Deussing JM, Hillard CJ, et al. Sustained glucocorticoid exposure recruits cortico-limbic CRH signaling to modulate endocannabinoid function. Psychoneuroendocrinology. 2016;66:151–8. doi: 10.1016/j.psyneuen.2016.01.004. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR107] 107.Cetinel S, Hancioğlu S, Sener E, Uner C, Kiliç M, Sener G, et al. Oxytocin treatment alleviates stress-aggravated colitis by a receptor-dependent mechanism. Regul Pept. 2010;160:146–52. doi: 10.1016/j.regpep.2009.11.011. [DOI] [PubMed] [Google Scholar]

[CR108] 108.Gadotti VM, Zamponi GW. Anxiolytic effects of the flavonoid luteolin in a mouse model of acute colitis. Mol Brain. 2019;12:114. doi: 10.1186/s13041-019-0539-z. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR109] 109.Matisz CE, Vicentini FA, Hirota SA, Sharkey KA, Gruber AJ. Behavioral adaptations in a relapsing mouse model of colitis. Physiol Behav. 2020;216:112802. doi: 10.1016/j.physbeh.2020.112802. [DOI] [PubMed] [Google Scholar]

[CR110] 110.Patel S, Hill MN, Cheer JF, Wotjak CT, Holmes A. The endocannabinoid system as a target for novel anxiolytic drugs. Neurosci Biobehav Rev. 2017;76:56–66. doi: 10.1016/j.neubiorev.2016.12.033. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR111] 111.Flannery LE, Kerr DM, Finn DP, Roche M. FAAH inhibition attenuates TLR3-mediated hyperthermia, nociceptive- and anxiety-like behaviour in female rats. Behav Brain Res. 2018;353:11–20. doi: 10.1016/j.bbr.2018.06.030. [DOI] [PubMed] [Google Scholar]

[CR112] 112.Doenni VM, Gray JM, Song CM, Patel S, Hill MN, Pittman QJ. Deficient adolescent social behavior following early-life inflammation is ameliorated by augmentation of anandamide signaling. Brain Behav Immun. 2016;58:237–47. doi: 10.1016/j.bbi.2016.07.152. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR113] 113.Bedse G, Bluett RJ, Patrick TA, Romness NK, Gaulden AD, Kingsley PJ, et al. Therapeutic endocannabinoid augmentation for mood and anxiety disorders: comparative profiling of FAAH, MAGL and dual inhibitors. Transl Psychiatry. 2018;8:92. doi: 10.1038/s41398-018-0141-7. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR114] 114.Dantzer R, Konsman JP, Bluthé RM, Kelley KW. Neural and humoral pathways of communication from the immune system to the brain: parallel or convergent? Auton Neurosci. 2000;85:60–65. doi: 10.1016/S1566-0702(00)00220-4. [DOI] [PubMed] [Google Scholar]

[CR115] 115.Taché Y, Bonaz B. Corticotropin-releasing factor receptors and stress-related alterations of gut motor function. J Clin Invest. 2007;117:33–40. doi: 10.1172/JCI30085. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR116] 116.Franchimont D, Bouma G, Galon J, Wolkersdörfer GW, Haidan A, Chrousos GP, et al. Adrenal cortical activation in murine colitis. Gastroenterology. 2000;119:1560–8. doi: 10.1053/gast.2000.20235. [DOI] [PubMed] [Google Scholar]

[CR117] 117.Deiteren A, Vermeulen W, Moreels TG, Pelckmans PA, De Man JG, De Winter BY. The effect of chemically induced colitis, psychological stress and their combination on visceral pain in female Wistar rats. Stress. 2014;17:431–44. doi: 10.3109/10253890.2014.951034. [DOI] [PubMed] [Google Scholar]

[CR118] 118.Parolaro D. Presence and functional regulation of cannabinoid receptors in immune cells. Life Sci. 1999;65:637–44. doi: 10.1016/S0024-3205(99)00286-6. [DOI] [PubMed] [Google Scholar]

[CR119] 119.Nagarkatti P, Pandey R, Rieder SA, Hegde VL, Nagarkatti M. Cannabinoids as novel anti-inflammatory drugs. Future Med Chem. 2009;1:1333–49. doi: 10.4155/fmc.09.93. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR120] 120.D’Argenio G, Valenti M, Scaglione G, Cosenza V, Sorrentini I, Di Marzo V. Up-regulation of anandamide levels as an endogenous mechanism and a pharmacological strategy to limit colon inflammation. FASEB J. 2006;20:568–70. doi: 10.1096/fj.05-4943fje. [DOI] [PubMed] [Google Scholar]

[CR121] 121.Storr MA, Keenan CM, Emmerdinger D, Zhang H, Yüce B, Sibaev A, et al. Targeting endocannabinoid degradation protects against experimental colitis in mice: involvement of CB1 and CB2 receptors. J Mol Med. 2008;86:925–36. doi: 10.1007/s00109-008-0359-6. [DOI] [PubMed] [Google Scholar]

[CR122] 122.Fichna J, Bawa M, Thakur GA, Tichkule R, Makriyannis A, McCafferty D-M, et al. Cannabinoids alleviate experimentally induced intestinal inflammation by acting at central and peripheral receptors. PLoS One. 2014;9:e109115. doi: 10.1371/journal.pone.0109115. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR123] 123.Busquets-Garcia A, Puighermanal E, Pastor A, de la Torre R, Maldonado R, Ozaita A. Differential role of anandamide and 2-arachidonoylglycerol in memory and anxiety-like responses. Biol Psychiatry. 2011;70:479–86. doi: 10.1016/j.biopsych.2011.04.022. [DOI] [PubMed] [Google Scholar]

[CR124] 124.Kinsey SG, O’Neal ST, Long JZ, Cravatt BF, Lichtman AH. Inhibition of endocannabinoid catabolic enzymes elicits anxiolytic-like effects in the marble burying assay. Pharm Biochem Behav. 2011;98:21–27. doi: 10.1016/j.pbb.2010.12.002. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR125] 125.Sciolino NR, Zhou W, Hohmann AG. Enhancement of endocannabinoid signaling with JZL184, an inhibitor of the 2-arachidonoylglycerol hydrolyzing enzyme monoacylglycerol lipase, produces anxiolytic effects under conditions of high environmental aversiveness in rats. Pharm Res. 2011;64:226–34. doi: 10.1016/j.phrs.2011.04.010. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR126] 126.Sumislawski JJ, Ramikie TS, Patel S. Reversible gating of endocannabinoid plasticity in the amygdala by chronic stress: a potential role for monoacylglycerol lipase inhibition in the prevention of stress-induced behavioral adaptation. Neuropsychopharmacology. 2011;36:2750–61. doi: 10.1038/npp.2011.166. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR127] 127.Hauer D, Schelling G, Gola H, Campolongo P, Morath J, Roozendaal B, et al. Plasma concentrations of endocannabinoids and related primary fatty acid amides in patients with post-traumatic stress disorder. PLoS One. 2013;8:e62741. doi: 10.1371/journal.pone.0062741. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR128] 128.Domi E, Uhrig S, Soverchia L, Spanagel R, Hansson AC, Barbier E, et al. Genetic deletion of neuronal PPARγ enhances the emotional response to acute stress and exacerbates anxiety: an effect reversed by rescue of amygdala PPARγ function. J Neurosci. 2016;36:12611–23. doi: 10.1523/JNEUROSCI.4127-15.2016. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR129] 129.Mirza R, Sharma B. Selective modulator of peroxisome proliferator-activated receptor-α protects propionic acid induced autism-like phenotypes in rats. Life Sci. 2018;214:106–17. doi: 10.1016/j.lfs.2018.10.045. [DOI] [PubMed] [Google Scholar]

[CR130] 130.Russo R, Cristiano C, Avagliano C, De Caro C, La Rana G, Raso GM, et al. Gut-brain axis: role of lipids in the regulation of inflammation, pain and CNS diseases. Curr Med Chem. 2018;25:3930–52. doi: 10.2174/0929867324666170216113756. [DOI] [PubMed] [Google Scholar]

[CR131] 131.De Gregorio D, Manchia M, Carpiniello B, Valtorta F, Nobile M, Gobbi G, et al. Role of palmitoylethanolamide (PEA) in depression: Translational evidence: Special Section on ‘Translational and Neuroscience Studies in Affective Disorders’. Section Editor, Maria Nobile MD, PhD. This Section of JAD focuses on the relevance of translational and neuroscience studies in providing a better understanding of the neural basis of affective disorders. The main aim is to briefly summaries relevant research findings in clinical neuroscience with particular regards to specific innovative topics in mood and anxiety disorders. J Affect Disord. 2019;255:S0165-0327(18)31599-4. doi: 10.1016/j.jad.2018.10.117. [DOI] [PubMed] [Google Scholar]

[CR132] 132.Zhao Q, Wang Q, Wang J, Tang M, Huang S, Peng K, et al. Maternal immune activation-induced PPARγ-dependent dysfunction of microglia associated with neurogenic impairment and aberrant postnatal behaviors in offspring. Neurobiol Dis. 2019;125:1–13. doi: 10.1016/j.nbd.2019.01.005. [DOI] [PubMed] [Google Scholar]

[CR133] 133.Christofides A, Konstantinidou E, Jani C, Boussiotis VA. The role of peroxisome proliferator-activated receptors (PPAR) in immune responses. Metabolism. 2021;114:154338. doi: 10.1016/j.metabol.2020.154338. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR134] 134.D’Souza DC, Cortes-Briones J, Creatura G, Bluez G, Thurnauer H, Deaso E, et al. Efficacy and safety of a fatty acid amide hydrolase inhibitor (PF-04457845) in the treatment of cannabis withdrawal and dependence in men: a double-blind, placebo-controlled, parallel group, phase 2a single-site randomised controlled trial. Lancet Psychiatry. 2019;6:35–45. doi: 10.1016/S2215-0366(18)30427-9. [DOI] [PubMed] [Google Scholar]

[CR135] 135.Asratian A, Lindé J, Morena M, Haataja R, Hammar V. Elevated Anandamide, Enhanced Recall of Fear Extinction, and Attenuated Stress Responses Following Inhibition of Fatty Acid Amide Hydrolase: A Randomized, Controlled Experimental Medicine Trial. Biol Psychiatry. 2020;87:538–47. doi: 10.1016/j.biopsych.2019.07.034. [DOI] [PubMed] [Google Scholar]

[CR136] 136.Schmidt ME, Liebowitz MR, Stein MB, Grunfeld J, Van Hove I, Simmons WK, et al. The effects of inhibition of fatty acid amide hydrolase (FAAH) by JNJ-42165279 in social anxiety disorder: a double-blind, randomized, placebo-controlled proof-of-concept study. Neuropsychopharmacology. 2020. 10.1038/s41386-020-00888-1. [DOI] [PMC free article] [PubMed]

[CR137] 137.Fitzgibbon M, Finn DP, Roche M. High times for painful blues: the endocannabinoid system in pain-depression comorbidity. Int J Neuropsychopharmacol. 2015;19:pyv095. doi: 10.1093/ijnp/pyv095. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR138] 138.Doeve BH, van de Meeberg MM, van Schaik FDM, Fidder HH A systematic review with meta-analysis of the efficacy of cannabis and cannabinoids for inflammatory bowel disease: what can we learn from randomized and nonrandomized studies? J Clin Gastroenterol. 2020. 10.1097/MCG.0000000000001393. [DOI] [PubMed]

PERMALINK

Comorbid anxiety-like behavior in a rat model of colitis is mediated by an upregulation of corticolimbic fatty acid amide hydrolase

Haley A Vecchiarelli

Maria Morena

Catherine M Keenan

Vincent Chiang

Kaitlyn Tan

Min Qiao

Kira Leitl

Alessia Santori

Quentin J Pittman

Keith A Sharkey

Matthew N Hill

Abstract

Introduction

Methods and materials

Animals

Colitis induction and assessment

Behavioral measures

Locomotor activity

Elevated plus maze (EPM)

Biochemical and molecular measures

Corticosterone enzyme-linked immunosorbent assay (ELISA)

Endocannabinoid measurements

Enzyme activity assays

Gene expression analysis

Pharmacological intervention - behavioral studies

Pharmacological intervention - biochemical studies

Statistical analyses

Results

Colitis induction produced behavioral indices of increased anxiety-like behavior

Fig. 1. TNBS-induced colitis phenotype.

Fig. 2. TNBS-induced colitis leads to anxiety-like behavior in the EPM at Day 7 post-administration.

TNBS-induced colitis altered central endocannabinoid levels

Fig. 3. Colitis altered central endocannabinoid levels.

Central FAAH inhibition reversed colitis-induced anxiety-like behavior

Fig. 4. Central FAAH inhibition reversed colitis-induced anxiety-like behavior.

Central CRF-R1 signaling regulates colitis-induced alterations in AEA

Fig. 5. Colitis-induced reductions in AEA levels were mediated by CRF-R1.

TNBS-colitis also reduced central AEA levels in female rats

Discussion

Funding and disclosures

Supplementary information

Acknowledgements

Author contributions

Footnotes

Contributor Information

Supplementary information

References

Associated Data

Supplementary Materials

ACTIONS

PERMALINK

RESOURCES

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