Skip to main content
PMC home page
Experimental and Therapeutic Medicine logoLink to Experimental and Therapeutic Medicine
. 2020 Apr 23;20(1):671–677. doi: 10.3892/etm.2020.8680

Hydrogen sulfide alleviates cognitive deficiency and hepatic dysfunction in a mouse model of acute liver failure

Da-Sen Yuan 1,*, Yue-Qi Huang 1,*, Yuan-Ji Fu 1,*, Juan Xie 1, Yuan-Lu Huang 1, Shi-Shan Zhou 1, Pei-Yuan Sun 1, Xiao-Qing Tang 1,✉
PMCID: PMC7271739  PMID: 32509026

Abstract

Acute liver failure (ALF) is a devastating clinical syndrome with a high mortality rate if not treated promptly. Previous studies have demonstrated the beneficial effects of hydrogen sulfide (H2S) on the brain and liver. The present study aimed to investigate the potential protective effects of H2S in ALF. A mouse model of ALF was established following treatment with thioacetamide (TAA). Mice with TAA-induced ALF were intraperitoneally injected with 30 or 100 µmol/kg/day sodium hydrosulfide (NaHS; a H2S donor drug) for two weeks. According to results from novel object recognition and Y-maze tests, in the present study, NaHS treatment alleviated cognitive deficiency and preserved spatial orientation learning ability in TAA-induced ALF mice compared with those of untreated mice. In addition, NaHS treatment reduced serum levels of aspartate transaminase (AST), alanine transaminase (ALT) and the concentration of ammonia compared with those that received control treatment, resulting in weight loss prevention. These findings suggested a beneficial effect of H2S on liver function. In conclusion, results from the present study suggested that H2S treatment may alleviate cognitive deficiency and hepatic dysfunction in mice with ALF, indicating the potential therapeutic benefits of applying H2S for the treatment of ALF.

Keywords: acute liver failure, cognition, hydrogen sulfide, novel object recognition test, Y-maze test

Introduction

Acute liver failure (ALF) is a devastating clinical syndrome that is associated with a high mortality rate if not treated promptly (1). Originally termed fulminant hepatic failure, ALF is defined as severe liver injury that is potentially reversible in nature with the onset of hepatic encephalopathy (HE) occurring within 8 weeks of the first symptoms in the absence of any pre-existing liver diseases (2). Patients ALF with HE present with various neuropsychiatric symptoms, including cognitive deficiency, motor function impairment and alterations in personality and consciousness (3,4). Although the most effective therapy for ALF is liver transplantation, due to the side effects associated with immunosuppressant therapy and the shortage of donor organs, this procedure is limited at present (5,6). Therefore, further investigation into novel approaches for the treatment of ALF is urgently sorted.

Hydrogen sulfide (H2S) was previously known only for its unpleasant odor; however, an increasing number of studies have revealed that endogenously produced H2S serves a protective role in a number of physiological functions (7). Numerous enzymes, including cystathionine-γ-lyase (CSE), cystathionine-β-synthase and 3-mercaptopyruvate sulfurtransferase are responsible for H2S synthesis (8). In the liver, endogenously produced H2S participates in the regulation of liver glucose metabolism, lipoprotein synthesis, hepatic circulation, liver bioenergetics and oxidative stress (8). A number of studies have previously revealed the protective effects of H2S in multiple models of hepatic diseases, including liver cirrhosis and fibrosis (9), portal hypertension (10) and hepatic ischemia-reperfusion (I/R) injury (11). In addition, H2S has also been demonstrated to be a novel signaling molecule and neuromodulator in the central nervous system (12). Previous evidence has indicated that H2S protects neurons from oxidative stress and impairments of learning and memory in models of Alzheimer's disease (13,14). Therefore, it could be hypothesized that H2S may also exert protective role son mouse models of ALF, with combined effects on both the brain and liver.

In the present study, ALF was induced in mice by thioacetamide (TAA) treatment, where sodium hydrosulfide (NaHS) served as the H2S donor. The results of the present study revealed that H2S treatment alleviated cognitive deficiency and preserved spatial orientation learning ability as assessed by novel object recognition (NOR) and Y-maze tests, respectively. In addition, H2S treatment reduced serum aspartate transaminase (AST), alanine transaminase (ALT) and ammonia levels and prevented weight loss following ALF induction. These results suggested a protective effect of H2S in ALF-model mice, indicating that H2S may serve as a potential therapeutic agent for ALF.

Materials and methods

Animals

A total of 100 female Institute of Cancer Research mice (age, 8 weeks; weight, 30±2 g) were provided by the Hunan SJA Laboratory Animals Co., Ltd. and were housed individually in a well-ventilated and temperature-controlled room (temperature, 25˚C; humidity, 50%) under a 12-h light/dark cycle, with free access to food and water. The mice had 7 days to habituate to their new environment before they were subjected to experiments. All experiments were conducted in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals (15) and were approved by the Animal Use and Protection Committee of the University of South China (Hengyang, China). All efforts were made to minimize the number of animals used and their suffering.

Drugs and treatments

NaHS, the H2S donor and TAA were purchased from Sigma-Aldrich; Merck KGaA. NaHS and TAA were dissolved in phosphate buffered saline (PBS) and sterile normal saline solutions, respectively. Following 7 days of adaptation, the mice were randomly divided into five treatment groups (n=20 per group; Fig. 1): i) The control group, in which mice were injected intraperitoneally with PBS for 14 days; ii) the TAA-alone-treatment group, in which mice were injected intraperitoneally with 150 mg/kg/day TAA for 3 days; iii) the co-treatment with TAA and 30 µmol/kg/day NaHS group, in which mice were pre-treated with 30 µmol/kg/day NaHS for 11 days and subsequently co-treated with 150 mg/kg/day TAA for 3 days; iv) the co-treatment with TAA and 100 µmol/kg/day NaHS group, in which the mice were pre-treated with 100 µmol/kg/day NaHS for 11 days and subsequently co-treated with 150 mg/kg/day TAA for 3 days; and v) the NaHS-alone-treated group, in which mice were injected intraperitoneally with 100 μmol/kg/day NaHS for 14 days. A well-established model of TAA-induced ALF was used (16-18). Following TAA injection for 24 h, all animals, including those in the control group, were subcutaneously injected with 0.5 ml solution containing 0.45% NaCl, 5% dextrose and 0.2% KCl to prevent the development of hypovolemia, hypoglycemia and hypokalemia, respectively. Hypothermia was prevented by intermittent exposure to infrared light in a procedure described previously (19,20).

Figure 1.

Figure 1

Open in a new tab

Schematic diagram of the experimental schedule. NOR, novel object recognition test; TAA, thioacetamide; NaHS, sodium hydrosulfide.

Survival analysis after TAA challenge

Survival rates in each group were recorded on the mornings of days 15-18. Housing was maintained at a temperature of 25˚C and relative humidity of 50% to reduce animal suffering. Baseline body weight was measured at 8:00 am on the first day of TAA injection and body weight was subsequently recorded three times per day (at the beginning of the day and every 6 h between 8:00 am and 8:00 pm). Animals were euthanized by sodium pentobarbital overdose (100 mg/kg, intravenous injection) when a reduction of >20% baseline body weight was observed. All mice were euthanized when all the measurements were completed.

NOR test

Mice cognitive function was assessed by using a novel objection recognition analysis system (BW-NOD405; Shanghai Biowill Co., Ltd.). NOR test was performed once per day after the induction of ALF. The NOR test included three trials. In the habituation phase, all mice were habituated in a 38x38x38 cm test box for 2 days. All individuals were allowed to explore the empty arena for 5 min once per day. On day 3 of the NOR test, the mice were allowed to explore two identical objects that were placed at opposite corners of the box for 5 min, in a process known as the familiarization phase. Following a 1-h retention interval, the mice underwent a test session in the box with one familiar and one novel object. Each animal was allowed to explore the objects for 5 min, where the exploration time spent for each object was recorded. Ethanol (75% v/v) was used to wipe the objects and the test apparatus prior to each test to avoid olfactory cue formation. Sniffing and touching of the objects (distance within 1 cm) were considered exploratory behaviors, whilst climbing on the objects or chewing were not. Discrimination index, which was calculated as the time difference between new and familiar object exploration/total time, was adopted to evaluate animal cognitive function (21,22).

Y-maze test

Spatial orientation learning ability was assessed by using a Y-maze analysis system (BW-MYM103; Shanghai Biowill Co., Ltd.). The Y-maze test was performed 4 days following the induction of ALF. The Y-maze was divided into three arms (A, B and C) with an angle of 120˚ between them. The size of each arm was 50x18x35 cm. Each mouse was habituated in the Y-maze for 10 min prior to the test. Subsequently, the mice were placed into the first arm and allowed to move freely for 5 min. Arm entry was recorded when all four limbs of the mouse completely entered the arm. The appropriate alternating sequence was defined as three consecutive entries made into the different arms, whilst animals that entered the same arm three times consecutively were considered to have performed an incorrect alternating sequence. Ethanol (75% v/v) was used to wipe the objects and the test apparatus prior to each test in order to remove olfactory cues. A spontaneous alternation score was estimated to measure spatial orientation learning ability (23).

Serum ammonia and liver enzymes

Blood samples (500 µl) were obtained from each mouse via the orbital vein after Y maze test under anesthesia with an intraperitoneal injection of sodium pentobarbital (50 mg/kg). After blood extraction, all mice were euthanized by sodium pentobarbital overdose (100 mg/kg, intravenous injection). ALT, AST and ammonia levels were analyzed in glass tubes, following the Y-maze test. Serum samples were centrifuged (speed, 1006.2 x g; temperature, 37˚C) for 5 min and analyzed on the day of sampling using a Hitachi 7600 series Automatic Analyzer (Hitachi, Ltd.). All serum samples were processed in the same laboratory using the same methods and reference values.

Statistical analysis

Statistical analysis was performed using the SPSS 18.0 software (SPSS, Inc.). The data are presented as the mean ± SEM. One-way ANOVA with the least-significant difference multiple comparison test (where there were 3 groups) or Tukey's post hoc test (where there were >4 groups) was performed. Kaplan-Meier survival analysis was performed using the Cox proportional hazards regression and the Log-rank test. Weight data was processed using mixed-design ANOVA and one-way ANOVA, following which Bonferroni's test was used as the post hoc test for simple main effects. P<0.05 was considered to indicate a statistically significant difference.

Results

TAA induces cognitive deficiency as demonstrated by the NOR and Y-maze tests

NOR and Y-maze tests were performed to evaluate mouse cognitive function following and prior to TAA treatment (150 mg/kg, intraperitoneally). The NOR test revealed that the discrimination index in TAA-treated mice was significantly reduced following TAA injection compared with that in the TAA group prior to injection (Fig. 2B). However, no significant difference was observed between the total time spent exploring the novel object prior to and following TAA injection (Fig. 2A). In the Y-maze test, the number of spontaneous alternations made by mice were found to be significantly decreased following TAA treatment compared with those prior to TAA treatment (Fig. 2D), whilst no significant differences were observed in the number of total entries made by the mice prior to and following TAA injection (Fig. 2C). These results suggest that TAA treatment resulted in cognitive deficiency.

Figure 2.

Figure 2

Open in a new tab

Effect of TAA on mouse cognitive function in the NOR and Y-maze tests. The NOR and Y-maze tests were adopted to evaluate cognitive function before and after TAA administration. (A) The total object exploration time and (B) discrimination index in the test period were recorded for each mouse. The NOR test results are presented as the mean ± SEM. n=8-9. (C) The total number of arm entries and (D) spontaneous alternations were recorded for each mouse. Y-maze test values are presented as the mean ± SEM. n=9-15. *P<0.05 vs. TAA, before TAA injection. NOR, novel object recognition test; TAA, thioacetamide.

H2S improves the survival rate of TAA-treated mice

The results of the present study revealed that 6 of the 20 mice did not survive to day 18 following TAA administration (150 mg/kg, intraperitoneally), whilst all mice in the control group were viable. NaHS treatment (100 µmol/kg/day, intraperitoneally) significantly reduced the mortality rate in the co-treatment group, where 1 of the 20 mice did not survive (P=0.046; Fig. 3). These results demonstrated that H2S treatment improved the survival rates of ALF mice.

Figure 3.

Figure 3

Open in a new tab

Effect of NaHS treatment on the survival rates of mice. The mortality rates in each group were recorded from days 15 to 18 after TAA treatment. n=20. *P<0.05, TAA vs. TAA + NaHS (100 µmol/kg). NaHS, sodium hydrogen sulfide; TAA, thioacetamide.

H2S prevents weight loss in TAA-treated mice

To assess weight changes in the mice among the treatment groups over time, a mixed ANOVA was conducted. The results showed that the main effect of treatment regimen was not significantly different (F=0.549; P=0.76) and the subsequent post-hoc test for the main effects of treatment regimen also did not reveal any significant differences. However, the main effect of time (F=34.609; P<0.001) and the interaction between time and treatment regimen (F=7.987; P<0.001) were found to be significantly different. For the interaction between time and treatment regimen, one-way ANOVA measuring the independent effects of treatment regimen at a specific time point was performed. There was no significant difference among the treatment regimens on days 11-13. However, on day 14, TAA treatment (150 mg/kg, intraperitoneally) significantly reduced the body weight of the animals compared with that of control animals (Fig. 4A), whilst NaHS treatment (100 µmol/kg/day, intraperitoneally) prevented weight loss in TAA-treated mice compared with mice in the TAA-treatment alone group (P=0.017; Fig. 4B). In addition, no significant differences were noted in the body weight between the mice in the control and those in the H2S-alone-treated groups (Fig. 4C). These results suggest that H2S pre-treatment prevented weight loss in ALF mice.

Figure 4.

Figure 4

Open in a new tab

Effect of H2S on the body weight of each mouse. Weight changes were recorded in the mornings from days 11 to 14 after TAA treatment. (A) Comparison between control and TAA groups, (B) comparison among TAA-treated-alone goup and co-treatment with TAA and NaHS (30 and 100 µmol/kg/day, intraperitoneally) groups, and (C) comparison between control and NaHS (100 µmol/kg/day, intraperitoneally) groups. Values are presented as the mean ± SEM. n=9-15. ***P<0.001 vs. control; *P<0.05 vs. TAA. H2S, hydrogen sulfide; TAA, thioacetamide; NaHS, sodium hydrogen sulfide.

H2S attenuates cognitive deficiency as determined by the NOR test

In the present study, the effect of H2S treatment on TAA-induced cognitive dysfunction was subsequently investigated. The mice were pre-treated with NaHS for 11 days and co-treated with TAA for an additional 3 days, following which cognitive function was investigated using the NOR test. No significant differences were noted in the time of total object exploration among the five groups of mice (Fig. 5A). The discrimination index in the TAA-treated mice were found to be significantly decreased compared with that noted in the control group (Fig. 5B). However, NaHS treatment (30 or 100 µmol/kg/day, intraperitoneal administration) significantly increased the discrimination index compared with that in the TAA treatment alone group (Fig. 5B). These results suggested that H2S ameliorated cognitive deficiency triggered by the TAA injection.

Figure 5.

Figure 5

Open in a new tab

Effect of H2S on the novel object recognition ability of mice following TAA treatment. After treatment with saline or NaHS (30 and 100 µmol/kg/day, intraperitoneally) for 11 days followed by co-treatment with TAA (150 mg/kg, intraperitoneally) for 3 days, the mice were subjected to novel object recognition test. (A) The total object exploration time and (B) discrimination index in the test period were recorded for each mouse. Values are presented as the mean ± SEM n=8-9. *P<0.05 vs. control; #P<0.05 vs. TAA. NaHS, sodium hydrogen sulfide; TAA, thioacetamide.

H2S improves spatial orientation learning ability in the Y-maze test

To investigate further whether H2S treatment improved the spatial orientation learning ability of mice with ALF, the animals were subjected to the Y-maze test. No significant differences were observed in the number of total entries among the 5 groups of mice (Fig. 6A). Spontaneous alternations in the TAA-treated mice were revealed to be significantly decreased compared with those noted in the control group (Fig. 6B). However, NaHS administration (100 µmol/kg/day, intraperitoneally) increased the spontaneous alternations in the TAA-treated mice compared with those treated with TAA alone. The results suggested that H2S treatment protected mice from spatial orientation learning ability impairment triggered by TAA administration.

Figure 6.

Figure 6

Open in a new tab

Effect of H2S on the spatial orientation learning ability of mice. After treatment with saline or NaHS (30 and 100 µmol/kg/day, intraperitoneally) for 11 days followed by co-treatment with TAA (150 mg/kg, intraperitoneally) for 3 days, respectively, the mice were subjected to the Y-maze test. (A) The total number of arm entries and (B) spontaneous alternations were recorded. Values are presented as the mean ± SEM. n=9-15. *P<0.05 vs. control; ##P<0.01 vs. TAA. H2S, hydrogen sulfide; TAA, thioacetamide; NaHS, sodium hydrogen sulfide.

H2S decreased serum levels of ALT, AST and ammonia after TAA treatment

AST, ALT and ammonia serum levels were next measured among the five groups. TAA administration (150 mg/kg, intraperitoneally) resulted in significant increases in serum ALT, AST and ammonia levels in comparison with control treatment (Fig. 7A-C). TAA co-administration in the presence of NaHS (100 µmol/kg/day, intraperitoneally) caused significant reductions in the serum levels of ALT, AST and ammonia compared with TAA alone (Fig. 7A-C). These results suggested that H2S treatment reduced liver dysfunction induced by TAA administration.

Figure 7.

Figure 7

Open in a new tab

Effect of H2S on the serum levels of liver enzymes and ammonia in mice. The serum levels of (A) ALT, (B) AST, and (C) ammonia were measured on the last day of the experiment. Values are presented as the mean ± SEM. n=6-9. *P<0.05 vs. control; **P<0.01 vs. control; #P<0.05 vs. TAA; ##P<0.01 vs. TAA. ALT, alanine transaminase; AST, aspartate transaminase; TAA, thioacetamide; NaHS, sodium hydrogen sulfide.

Discussion

TAA administration induces ALF, leading to cognitive deficiency and hepatic dysfunction in mice (17,24). Previous studies have provided evidence that endogenous H2S exerts a series of protective effects on the brain and liver (25-27). The aim of the present study was to investigate the role of H2S treatment in TAA-induced mouse models of ALF where the potential therapeutic value of H2S in this mouse model was also evaluated. The main findings were as follows: i) H2S treatment appeared to alleviate cognitive deficiency and preserve spatial orientation learning ability in mice treated with TAA according to NOR and Y-maze test data, respectively; and ii) H2S treatment appeared to reduce serum levels of ALT, AST and ammonia, in addition to preventing weight loss in TAA-treated mice. Therefore, H2S treatment is suggested to exhibit protective effects on both brain and liver function in ALF mice.

TAA-induced ALF is a well-established rodent ALF model (28). The Y-maze and NOR tests are widely used as robust assays for assessing the cognitive function in mice (28). In the NOR test, NaHS administration led to marked increases in the discrimination index in the TAA-treated mice compared with mice treated with TAA alone, suggesting a protective effect of H2S on cognition. The protective action of H2S on cognition was confirmed further according to data obtained using the Y maze test. Compared with the control treatment, TAA treatment resulted in a reduction in spontaneous alternation, an effect that was reversed by H2S treatment. These findings suggest that H2S alleviated cognitive deficiency induced by TAA. A previous study conducted by our group (23) indicated that H2S application ameliorated cognitive dysfunction in a chronic restrain stress (CRS)-induced rat model, where H2S reversed the production of malondialdehyde and the reductions in superoxide dismutase activity and glutathione levels, demonstrating that it could protect against CRS-induced oxidative stress in the brain. To uncover the underlying molecular mechanisms of this protective action of H2S further, additional biochemical experiments are required in future studies.

The serum levels of ALT and AST are sensitive markers for measuring liver injury (10,29). To investigate the effect of H2S on liver function, the serum levels of ALT, AST and ammonia were measured. H2S significantly reduced the serum levels of ALT and AST, suggesting that H2S exerted a hepato-protective effect. However, in a previous study, NaHS administration (0.15 mmol/kg, intraperitoneally) in rats augmented ALT and AST serum levels in the TAA-treatment group, suggesting that H2S treatment aggravated liver injury and manifested hepatotoxic effects (30). Different NaHS concentrations may be the cause of the aforementioned discrepancies. A previous study reported that NaHS administration in mice resulted in increased liver myeloperoxidase (MPO) activity, which is a marker of tissue neutrophil infiltration and tumor necrosis factor-α levels in the plasma (31). These results indicated a pro-inflammatory effect of H2S. By contrast, administration of the CSE inhibitor DL-propargylglycine (50 mg/kg; intraperitoneally) exhibited marked anti-inflammatory activity by reducing liver MPO activity and tissue damage (31). In addition, H2S has been reported to induce a biphasic concentration-dependent effect (32). In the present study, it was observed that NaHS treatment (30 or 100 µmol/kg/day, intraperitoneal administration) manifested neuroprotective effects on TAA-treated mice, consistent with the previous study (33). Therefore, low and increased levels of H2S exhibited cytoprotective and cytotoxic effects, respectively (34). HE is a common complication in patients with ALF, which is associated with poor prognosis (35). Hyperammonemia is strongly implicated in the pathogenesis of hepatic encephalopathy that can cause brain edema, oxidative stress and inflammation (36). Hyperammonemia can also affect hepatocyte function (37). The present study indicated that H2S treatment reversed the increased serum ammonia levels in TAA-treated mice, suggesting that H2S treatment inhibited the development of hepatic encephalopathy by preserving liver function. Histological analysis in an ALF model will be performed in future research, to verify the aforementioned conclusions.

The present study did not directly measure H2S levels, which is considered a limitation and should be assessed in a future study. Additionally, H2S pretreatment for 11 days can be considered excessive, where H2S concentration in the body may have been compensated for before TAA injection. Follow-up studies should therefore assess H2S concentrations in the blood and liver tissues or cerebrospinal fluid, in addition to adjusting the H2S pretreatment time. In the present study, NaHS was applied as the donor of H2S. Interestingly, Shirozu et al (6) reported that sodium thiosulfate, another donor of H2S, also attenuated liver injury in mouse models of acute liver failure. Therefore, sodium thiosulfate could have been adopted as an alternative donor of H2S in a further study.

In conclusion, the present study demonstrated that H2S treatment alleviated cognitive deficiency and hepatic impairment in an ALF mouse model. The current findings indicate that H2S treatment exerts combined beneficial effects on the brain and liver in ALF mice, which may serve as a protective molecule against ALF. However, the precise mechanisms underlying the protective effect of H2S in ALF remain elusive. Future studies should examine the molecular mechanisms underlying the aforementioned physiological processes. In addition, clinical studies are required to determine the potential clinical application of H2S in the therapy of ALF.

Acknowledgements

Not applicable.

Funding

The presrnt study was supported by a Project of Research-based Learning and Innovative Experiments for Undergraduate Students grant (grant no. 2018XJXZ145).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding authors on reasonable request.

Authors' contributions

DSY, YQH, YJF, JX, YLH, SSZ, and PYS performed the experiments and analyzed the data. XQT was accountable for all the aspects of the work and responsible for final approval of the version to be published. DSY, YQH, YJF and XQT were responsible for manuscript writing and revision and experimental design. All authors approved the final version of the manuscript and figures.

Ethics approval and consent to participate

All experiments were conducted in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals and were approved by the Animal Use and Protection Committee of the University of South China (approval no. 1807022; Hengyang, China).

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References

  • 1.Stravitz RT, Kramer AH, Davern T, Shaikh AO, Caldwell SH, Mehta RL, Blei AT, Fontana RJ, McGuire BM, Rossaro L, et al. Acute Liver Failure Study Group: Intensive care of patients with acute liver failure: Recommendations of the U.S. Acute Liver Failure Study Group. Crit Care Med. 2007;35:2498–2508. doi: 10.1097/01.CCM.0000287592.94554.5F. [DOI] [PubMed] [Google Scholar]
  • 2.Trey C, Davidson CS. The management of fulminant hepatic failure. Prog Liver Dis. 1970;3:282–298. [PubMed] [Google Scholar]
  • 3.Felipo V. Hepatic encephalopathy: Effects of liver failure on brain function. Nat Rev Neurosci. 2013;14:851–858. doi: 10.1038/nrn3587. [DOI] [PubMed] [Google Scholar]
  • 4.Poordad FF. Presentation and complications associated with cirrhosis of the liver. Curr Med Res Opin. 2015;31:925–937. doi: 10.1185/03007995.2015.1021905. [DOI] [PubMed] [Google Scholar]
  • 5.Lee WM. Acute liver failure. N Engl J Med. 1993;329:1862–1872. doi: 10.1056/NEJM199312163292508. [DOI] [PubMed] [Google Scholar]
  • 6.Shirozu K, Tokuda K, Marutani E, Lefer D, Wang R, Ichinose F. Cystathionine γ-lyase deficiency protects mice from galactosamine/lipopolysaccharide-induced acute liver failure. Antioxid Redox Signal. 2014;20:204–216. doi: 10.1089/ars.2013.5354. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Chen WL, Xie B, Zhang C, Xu KL, Niu YY, Tang XQ, Zhang P, Zou W, Hu B, Tian Y. Antidepressant-like and anxiolytic-like effects of hydrogen sulfide in behavioral models of depression and anxiety. Behav Pharmacol. 2013;24:590–597. doi: 10.1097/FBP.0b013e3283654258. [DOI] [PubMed] [Google Scholar]
  • 8.Mani S, Cao W, Wu L, Wang R. Hydrogen sulfide and the liver. Nitric Oxide. 2014;41:62–71. doi: 10.1016/j.niox.2014.02.006. [DOI] [PubMed] [Google Scholar]
  • 9.Fiorucci S, Antonelli E, Mencarelli A, Orlandi S, Renga B, Rizzo G, Distrutti E, Shah V, Morelli A. The third gas: H2S regulates perfusion pressure in both the isolated and perfused normal rat liver and in cirrhosis. Hepatology. 2005;42:539–548. doi: 10.1002/hep.20817. [DOI] [PubMed] [Google Scholar]
  • 10.Tan G, Pan S, Li J, Dong X, Kang K, Zhao M, Jiang X, Kanwar JR, Qiao H, Jiang H, Sun X. Hydrogen sulfide attenuates carbon tetrachloride-induced hepatotoxicity, liver cirrhosis and portal hypertension in rats. PLoS One. 2011;6(e25943) doi: 10.1371/journal.pone.0025943. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Kang K, Zhao M, Jiang H, Tan G, Pan S, Sun X. Role of hydrogen sulfide in hepatic ischemia-reperfusion-induced injury in rats. Liver Transpl. 2009;15:1306–1314. doi: 10.1002/lt.21810. [DOI] [PubMed] [Google Scholar]
  • 12.Tan BH, Wong PT, Bian JS. Hydrogen sulfide: A novel signaling molecule in the central nervous system. Neurochem Int. 2010;56:3–10. doi: 10.1016/j.neuint.2009.08.008. [DOI] [PubMed] [Google Scholar]
  • 13.Giuliani D, Ottani A, Zaffe D, Galantucci M, Strinati F, Lodi R, Guarini S. Hydrogen sulfide slows down progression of experimental Alzheimer's disease by targeting multiple pathophysiological mechanisms. Neurobiol Learn Mem. 2013;104:82–91. doi: 10.1016/j.nlm.2013.05.006. [DOI] [PubMed] [Google Scholar]
  • 14.Xuan A, Long D, Li J, Ji W, Zhang M, Hong L, Liu J. Hydrogen sulfide attenuates spatial memory impairment and hippocampal neuroinflammation in beta-amyloid rat model of Alzheimer's disease. J Neuroinflammation. 2012;9(202) doi: 10.1186/1742-2094-9-202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory Animals: Guide for the Care and Use of Laboratory Animals, 8th edition. National Academies Press (US), Washington, DC, 2011. [Google Scholar]
  • 16.Zimmermann C, Ferenci P, Pifl C, Yurdaydin C, Ebner J, Lassmann H, Roth E, Hörtnagl H. Hepatic encephalopathy in thioacetamide-induced acute liver failure in rats: Characterization of an improved model and study of amino acid-ergic neurotransmission. Hepatology. 1989;9:594–601. doi: 10.1002/hep.1840090414. [DOI] [PubMed] [Google Scholar]
  • 17.Avraham Y, Grigoriadis N, Poutahidis T, Vorobiev L, Magen I, Ilan Y, Mechoulam R, Berry E. Cannabidiol improves brain and liver function in a fulminant hepatic failure-induced model of hepatic encephalopathy in mice. Br J Pharmacol. 2011;162:1650–1658. doi: 10.1111/j.1476-5381.2010.01179.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Avraham Y, Grigoriadis NC, Magen I, Poutahidis T, Vorobiav L, Zolotarev O, Ilan Y, Mechoulam R, Berry E. Capsaicin affects brain function in a model of hepatic encephalopathy associated with fulminant hepatic failure in mice. Br J Pharmacol. 2009;158:896–906. doi: 10.1111/j.1476-5381.2009.00368.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Panikashvili D, Simeonidou C, Ben-Shabat S, Hanus L, Breuer A, Mechoulam R, Shohami E. An endogenous cannabinoid (2-AG) is neuroprotective after brain injury. Nature. 2001;413:527–531. doi: 10.1038/35097089. [DOI] [PubMed] [Google Scholar]
  • 20.Avraham Y, Israeli E, Gabbay E, Okun A, Zolotarev O, Silberman I, Ganzburg V, Dagon Y, Magen I, Vorobia L, et al. Endocannabinoids affect neurological and cognitive function in thioacetamide-induced hepatic encephalopathy in mice. Neurobiol Dis. 2006;21:237–245. doi: 10.1016/j.nbd.2005.07.008. [DOI] [PubMed] [Google Scholar]
  • 21.Li M, Zhang P, Wei HJ, Li MH, Zou W, Li X, Gu HF, Tang XQ. Hydrogen sulfide ameliorates homocysteine-induced cognitive dysfunction by inhibition of reactive aldehydes involving upregulation of ALDH2. Int J Neuropsychopharmacol. 2017;20:305–315. doi: 10.1093/ijnp/pyw103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Ye T, Meng X, Wang R, Zhang C, He S, Sun G, Sun X. Gastrodin alleviates cognitive dysfunction and depressive-like behaviors by inhibiting ER stress and NLRP3 inflammasome activation in db/db mice. Int J Mol Sci. 2018;19(E3977) doi: 10.3390/ijms19123977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Li XN, Chen L, Luo B, Li X, Wang CY, Zou W, Zhang P, You Y, Tang XQ. Hydrogen sulfide attenuates chronic restrain stress-induced cognitive impairment by upreglulation of Sirt1 in hippocampus. Oncotarget. 2017;8:100396–100410. doi: 10.18632/oncotarget.22237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Avraham Y, Zolotarev O, Grigoriadis NC, Poutahidis T, Magen I, Vorobiav L, Zimmer A, Ilan Y, Mechoulam R, Berry EM. Cannabinoids and capsaicin improve liver function following thioacetamide-induced acute injury in mice. Am J Gastroenterol. 2008;103:3047–3056. doi: 10.1111/j.1572-0241.2008.02155.x. [DOI] [PubMed] [Google Scholar]
  • 25.Wu DD, Wang DY, Li HM, Guo JC, Duan SF, Ji XY. Hydrogen Sulfide as a Novel Regulatory Factor in Liver Health and Disease. Oxid Med Cell Longev. 2019;2019(3831713) doi: 10.1155/2019/3831713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Chen WL, Niu YY, Jiang WZ, Tang HL, Zhang C, Xia QM, Tang XQ. Neuroprotective effects of hydrogen sulfide and the underlying signaling pathways. Rev Neurosci. 2015;26:129–142. doi: 10.1515/revneuro-2014-0051. [DOI] [PubMed] [Google Scholar]
  • 27.Panthi S, Chung HJ, Jung J, Jeong NY. Physiological Importance of Hydrogen Sulfide: Emerging Potent Neuroprotector and Neuromodulator. Oxid Med Cell Longev. 2016;2016(9049782) doi: 10.1155/2016/9049782. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Chen SM, Yi YL, Zeng D, Tang YY, Kang X, Zhang P, Zou W, Tang XQ. Hydrogen Sulfide Attenuates β2-Microglobulin-Induced Cognitive Dysfunction: Involving Recovery of Hippocampal Autophagic Flux. Front Behav Neurosci. 2019;13(244) doi: 10.3389/fnbeh.2019.00244. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Bae J, Min YS, Nam Y, Lee HS, Sohn UD. Humulus japonicus Extracts Protect Against Lipopolysaccharide/d-Galactosamine-Induced Acute Liver Injury in Rats. J Med Food. 2018;21:1009–1015. doi: 10.1089/jmf.2018.4178. [DOI] [PubMed] [Google Scholar]
  • 30.Wang X, Wang B, Huang Q, Zhang B, Hua Z. Regulation of hydrogen sulfide on transporter protein Bsep and Mdr2 in acute liver failure. Zhonghua Yi Xue Za Zhi. 2015;95:3176–3179. (In Chinese) [PubMed] [Google Scholar]
  • 31.Li L, Bhatia M, Zhu YZ, Zhu YC, Ramnath RD, Wang ZJ, Anuar FB, Whiteman M, Salto-Tellez M, Moore PK. Hydrogen sulfide is a novel mediator of lipopolysaccharide-induced inflammation in the mouse. FASEB J. 2005;19:1196–1198. doi: 10.1096/fj.04-3583fje. [DOI] [PubMed] [Google Scholar]
  • 32.Wedmann R, Bertlein S, Macinkovic I, Boltz S, Miljkovic J, Munoz LE, Herrmann M, Filipovic MR. Working with ‘H2S’: facts and apparent artifacts. Nitric Oxide. 2014;41:85–96. doi: 10.1016/j.niox.2014.06.003. [DOI] [PubMed] [Google Scholar]
  • 33.Yakovlev AV, Kurmasheva ED, Giniatullin R, Khalilov I, Sitdikova GF. Hydrogen sulfide inhibits giant depolarizing potentials and abolishes epileptiform activity of neonatal rat hippocampal slices. Neuroscience. 2017;340:153–165. doi: 10.1016/j.neuroscience.2016.10.051. [DOI] [PubMed] [Google Scholar]
  • 34.Brown KG, Strickland JA. Utilizing data from multiple studies (meta-analysis) to determine effective dose-duration levels. Example: Rats and mice exposed to hydrogen sulfide. Regul Toxicol Pharmacol. 2003;37:305–317. doi: 10.1016/s0273-2300(03)00007-2. [DOI] [PubMed] [Google Scholar]
  • 35.Schwendimann RN, Minagar A. Liver Disease and Neurology. Continuum (Minneap Minn) 2017;23 (3, Neurology of Systemic Disease):762–777. doi: 10.1212/CON.0000000000000486. [DOI] [PubMed] [Google Scholar]
  • 36.Shawcross D, Jalan R. The pathophysiologic basis of hepatic encephalopathy: Central role for ammonia and inflammation. Cell Mol Life Sci. 2005;62:2295–2304. doi: 10.1007/s00018-005-5089-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Wang Q, Wang Y, Yu Z, Li D, Jia B, Li J, Guan K, Zhou Y, Chen Y, Kan Q. Ammonia-induced energy disorders interfere with bilirubin metabolism in hepatocytes. Arch Biochem Biophys. 2014;555-556:16–22. doi: 10.1016/j.abb.2014.05.019. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding authors on reasonable request.

Articles from Experimental and Therapeutic Medicine are provided here courtesy of Spandidos Publications

RESOURCES