Abstract
Salidroside has anti-inflammatory, antioxidant and hepatoprotective properties. However, its effect on hepatic ischemia–reperfusion injury (IRI), an unavoidable side effect associated with liver transplantation, remains undefined. Here, we aimed to determine whether salidroside alleviates hepatic IRI and elucidate its potential mechanisms. We used both in vivo and in vitro assays to assess the effect and mechanisms of salidroside on hepatic IRI. Hepatic IRI rat models were pretreated with salidroside (5, 10 or 20 mg/kg/day) for 7 days following liver transplantation while hypoxia/reoxygenation (H/R) model of RAW 264.7 macrophages were pretreated with salidroside (1, 10 or 50 μM). The effect of salidroside on hepatic IRI was assessed using hematoxylin–eosin staining, terminal deoxynucleotidyl transferase dUTP nick-end labeling staining, qRT-PCR, immunosorbent assay and western blotting. Our in vivo assays showed that salidroside significantly reduced pathological liver damage, serum aminotransferase levels and serum levels of IL-1, IL-18 and TNF-α. Besides, salidroside reduced the expression of TLR-4/NF-κB/NLRP3 inflammatory pathway associated proteins (TLR-4, MyD88, p-IKKα, p-IKKβ, p-IKK, p-IκBα, p-P65, NLRP3, ASC, Cleaved caspase-1, IL-1β, IL-18, TNF-α and IL-6) in rats after liver transplantation. On the other hand, data from the in vitro analysis demonstrated that salidroside blocks expression of TLR-4/NF-κB/NLRP3 inflammatory pathway related proteins in the RAW264.7 cells treated with H/R. The salidroside-specific anti-inflammatory effects were partially inhibited by the TLR-4 agonist lipopolysaccharide. Taken together, our study showed that salidroside inhibits hepatic IRI following liver transplantation by modulating the TLR-4/NF-κB/NLRP3 inflammatory pathway.
Subject terms: Liver diseases, Liver
Introduction
Hepatic ischemia/reperfusion injury (IRI) is an unavoidable pathological event in many liver surgical procedures, especially liver transplantation1,2. Hepatic ischemia can cause metabolic problems and an inflammatory microenvironment in the liver, which could lead to graft rejection, hepatic pathological injury or apoptosis and early graft dysfunction3,4. The underlying pathogenesis of hepatic IRI is complicated, thus posing many barriers to early detection, diagnosis and treatment.
Previous studies have shown that innate immune system plays an important role in hepatic IRI, acting as the first line of defense against infection or injury by activating pattern recognition receptors (PRRs) such as Toll-like receptors (TLRs) as well as nucleotide-binding oligomerization domain-like receptors (NLRs)5,6. Primary TLRs expressed in hepatocytes and macrophages include TLR-2, TLR-3, TLR-4 and TLR-9 of which TLR-4 is involved in inflammatory responses caused by hepatic IRI7. TLR-4 signaling promotes MyD88-dependent pathways, which leads to the activation of nuclear factor kappa B (NF-κB), which is essential for production of proinflammatory cytokines8,9. Induction of the signaling pathway of NF-κB is one of the main mediators of inflammation and defines the development and progression of hepatic IRI10,11. As the most studied tissue-damage detector, the NLR family pyrin domain-containing 3 (NLRP3) inflammasome is composed of NLRP3, apoptosis-associated speck-like protein (ASC) and caspase-1, which is prominent in initiating and propagating the inflammatory responses12. Previous evidence suggests that the NF-κB signaling leads to NLRP3 activation that participates in the pathogenesis of hepatic IRI13. Thus, the TLR-4/NF-κB/NLRP3 inflammatory pathway might be involved in hepatic IRI.
Salidroside, a compound extracted from various Rhodiola plants, is widely used in treatment of ischemia stroke, Alzheimer’s disease, and cardiovascular diseases14,15. Recent data has shown that salidroside exerts a wide range of pharmacological activities, such as anti-hypoxia, anti-inflammation and antioxidant activity16,17. Furthermore, several studies have reported that salidroside could alleviate liver inflammation in furan-induced animals by modulating the NF-κB/NLRP3 signaling pathway, and plays a unique protective role in hepatic IRI18. In this study, we investigated the potential of salidroside to alleviate hepatic IRI and its underlying mechanisms using orthotopic liver transplant rat models.
Materials and methods
Ethical statement
All experiments were approved and performed in accordance with relevant institutional licensing committee guidelines and regulations (Ethics committee of Animal and Human Experimentation of Chongqing Medical University). The study was carried out in compliance with the ARRIVE guidelines. Euthanasia of animals is by CO2 exposure followed by cervical dislocation in compliance with the AVMA guidelines for the euthanasia of animals (2020).
Animals and orthotopic liver transplantation models
Chongqing Medical University's experimental animal center provided inbred male Sprague–Dawley rats (SD) (SPF grade, 220–250 g). The animals were kept in a pathogen-free environment. The rats were randomly divided into five groups, each with twelve animals (n = 12). We employed a unique magnetic anastomosis technique to perform orthotopic liver transplantation as previously described19. The sham group underwent abdominal incision to expose hepatic portal vein. After liver transplant, the rats in the ischemia reperfusion (I/R) group received no therapy. On the other hand, the rats in the I/R + Sal (5 mg/kg) group received salidroside (dissolved in 0.9 percent saline) (yuanyeBio, Shanghai, China) intraperitoneally for 7 days (5 mg/kg/day) before the surgery. The rats in the I/R + Sal (10 mg/kg) group were given salidroside (dissolved in 0.9 percent saline) intraperitoneally for 7 days (10 mg/kg/day) before the surgery. In addition, the rats in the I/R + Sal (20 mg/kg) group received salidroside (dissolved in 0.9 percent saline) intraperitoneally for 7 days (20 mg/kg/day) before the surgery. After orthotopic liver transplantation, the animals were euthanized at different times, and then liver tissues and sera were collected and frozen at − 80 °C.
In vitro study design and cell model
The RAW 264.7 cells were obtained from the Chinese Academy of Sciences' Type Culture Collection's Cell Bank and grown at 37 °C and 5% CO2 in F12/DMEM (Gibico Grand Island, USA) with 10% fetal bovine serum (Gibco, Australia). A hypoxia/reoxygenation (H/R) cell model was used to simulate hepatic IRI. Briefly, RAW 264.7 macrophages were placed in a tri-gas incubator (Thermo, MA, USA) with a 1% O2 and 5% CO2 condition. The cells were taken for additional tests after 6 h of hypoxia followed by 6 h of reoxygenation. With or without lipopolysaccharide (LPS) (25 mol/L, Beyotime, Shanghai, China), the cells were treated with 1, 10, or 50 M salidroside. Control cells were cultured in F12/DMEM (Gibico Grand Island, USA) containing 10% fetal bovine serum (Gibco, Australia) at 37 °C and 5% CO2.
Aminotransferase assay
Liver enzyme kits (Jiancheng Bioengineering Institute, China) were used to measure serum aminotransferase (AST) and aspartate aminotransferase (AST) levels, according to the manufacturer's instructions.
Determination of cytokines
Enzyme-linked immunosorbent assay (ELISA) kits were used to measure IL-1, IL-18, and tumor necrosis factor-α (TNF-α) in the cell culture supernatants and rat sera (Neobioscience, Beijing, China), following the manufacturers’ instructions.
Histology and TUNEL analysis
The grafts were fixed with 4% paraformaldehyde for 24 h. After being embedded, the tissues were sectioned at 5 µM and stained with HE. Suzuki scores were used to evaluate liver damage. The level of hepatic apoptosis was determined using a TUNEL kit (Beyotime, Shanghai, China), according to the manufacturer's protocol. An optical microscope (Lecia, Wetzlar, Germany) was used to analyze and image the tissues at different magnifications.
Western blot
Total protein from the liver tissues of rats following liver transplantation and RAW 264.7 cells from the Chinese Academy of Sciences' Type Culture Collection's Cell Bank was extracted by lysis in radio immunoprecipitation assay buffer with a proteinase inhibitor cocktail. The proteins were resolved in 10% SDS-PAGE gels before transfer into polyvinylidene fluoride membranes and then blocked for 15 min with blocking buffer. The membranes were treated overnight at 4 °C with primary antibodies (Table 1), washed and then incubated with secondary antibody for 1 h at room temperature. A gel imaging system was used to detect signals generated by chemiluminescence (ChemiScope 2850, Clinx Science, Shanghai, China). We then quantified the bands using ImageJ program.
Table 1.
Antibodies for immunofluorescence staining and western blot.
| Primary antibody | Dilution concentration | Supplier |
|---|---|---|
| TLR-4 | WB (1/300) | Abcam |
| MyD88 | WB (1/1000) | Abcam |
| p-IKKα | WB (1/1000) | Beyotime |
| IKKα | WB (1/1000) | Beyotime |
| p-IKKβ | WB (1/1000) | Beyotime |
| IKKβ | WB (1/1000) | Beyotime |
| p-IKK | WB (1/1000) | Beyotime |
| IKK | WB (1/1000) | Beyotime |
| p- IκBα | WB (1/2500) | Santa Cruz |
| IκBα | WB (1/2500) | Santa Cruz |
| p-P65 | WB (1/2500) | Beyotime |
| P65 | WB (1/1000) | Beyotime |
| NLRP3 | WB (1/1000) | Bioss |
| ASC | WB (1/1000) | Santa Cruz |
| Cleaved caspase-1 | WB (1/1000) | CST |
| Caspase-1 | WB (1/1000) | CST |
| IL-1β | WB (1/1000) | Beyotime |
| IL-18 | WB (1/1000) | Beyotime |
| TNF-α | WB (1/1000) | Beyotime |
| IL-6 | WB (1/1000) | Beyotime |
| β-actin | WB (1/1000) | Beyotime |
WB western blotting.
Quantitative real-time PCR (qRT-PCR)
Total RNA was extracted by TRIzol (Takara, Tokyo, Japan) according to the manufacturer's instructions, and then PrimeScript RT Reagent (Takara, Tokyo, Japan) was used to synthesize complementary DNA (cDNA). The PCR primers were provided by Sangon Biotech (Sangon Biotech, Shanghai, China), (Table 2). We used the 2−ΔΔCt method to evaluate all qRT-PCR samples, which were conducted in triplicate.
Table 2.
Primer sequences used for PCR analyses.
| Name | Forward primer | Reverse primer |
|---|---|---|
| TNF-α | CTACGTGCTCCTCACCCACACCGT | ACCTCAGCGCTGAGCAGGTCCCCC |
| IL-1β | AGGGCTGCTTCCAAACCTTTGACC | ACTGCCTGCCTGAAGCTCTTGTTG |
| IL-6 | CTGATTGTATGAACAGCGATGATG | AACTCCAGAAGACCAGAGCAGATT |
| IL-18 | GCAGTAATACGGAGCATAAA | ATCCTTCACAGATAGGGTCA |
| Ly6G | TGTGCAGAAAGAGCTCAGGGGCTGG | AGTGGGGCAGATGGGAAGGCAGAGA |
| CD11b | TGATTGATGGCTCCGGTAG | GGACTGTGGTTTGTTGAAGGC |
| GADPH | CTCACTCAAGATTGTCAGCA | GTCTTCTGGGTGGCAGTGAT |
Statistical analysis
The data was reported as the mean ± SD of at least three independent replicates. For comparisons involving means of two groups, the Student's t-test was used, while one-way ANOVA was utilized for comparisons of more than two groups. GraphPad Prism version 8.0 was used to conduct the data analyses. A p < 0.05 was used to indicate statistical significance.
Results
Salidroside enhances liver function and reduces inflammatory cytokines in rats after liver transplant
The rats were divided into three groups and received liver transplantation after salidroside intraperitoneally for 7 days (Fig. 1A). The chemical formula of salidroside is shown (Fig. 1B). Serum levels of AST and ALT are the main indicators in evaluating liver function. Our analysis showed that ALT and AST levels were significantly elevated after liver transplant. Pretreatment with increasing dosages of salidroside (5, 10, or 20 mg/kg) for 7 days decreased ALT and AST levels compared to the I/R group, demonstrating that salidroside treatment improves the recipients' liver functioning (Fig. 1C). The IL-1β, IL-18, and TNF-α serum levels were markedly higher in the I/R group compared to the control group. In comparison to the I/R group, salidroside pretreatment (5, 10 or 20 mg/kg) gradually suppressed the elevated levels of the cytokines (Fig. 1D).
Figure 1.
Salidroside improves liver function and decrease inflammatory cytokines in rats after liver transplantation. (A) Schematic diagram describing the grouping of the rats. (B) Chemical structure of salidroside. (C) Serum levels of ALT and AST in different groups. (D) Serum levels of inflammatory cytokines in different groups. The statistical differences among groups were assessed by one-way ANOVA. nsP > 0.05, *P < 0.05, **P < 0.01, ***P < 0.001.
Salidroside decreases histopathological changes in rats after liver transplant
To assess the function of salidroside in IRI-induced hepatocellular damage, HE staining was used examine the severity of histopathological changes in the liver from the rats in different groups. The HE staining data showed that the degree of coagulation necrosis, architectural anomalies, and hepatocyte vacuolization were milder in the I/R + Sal (5, 10 or 20 mg/kg) group. These findings showed that salidroside pretreatment significantly reduces IRI-induced hepatic pathological changes (Fig. 2A,C).
Figure 2.
Salidroside attenuates hepatic histopathological changes and hepatocyte apoptosis of the rats following liver transplantation. (A) Representative HE staining images showing hepatic histological alterations (indicated with arrowheads) in the rat liver (magnification, 200; scale bar, 200 m; n = 6). (B) Hepatic apoptosis detected by TUNEL assay (magnification, × 200; scale bar, 200 μm; n = 6). (C) Hepatic IRI grading based on suzuki’s grade. (D) TUNEL+ cells of the liver based on TUNEL assay. The statistical differences among groups were assessed by one-way ANOVA. nsP > 0.05, *P < 0.05, **P < 0.01, ***P < 0.001.
Salidroside attenuates hepatocyte apoptosis in rats following liver transplant
To investigate whether salidroside prevents hepatocyte apoptosis in vivo, the levels of hepatocyte apoptosis were determined using a TUNEL assay. The data demonstrated that the sham group had few TUNEL positive cells, which substantially increased following liver transplantation, consistent with the HE staining results. In contrast, salidroside pretreatment alleviated hepatic apoptosis in a dose-dependent manner (Fig. 2B,D).
Salidroside regulates the TLR-4/NF-κB/NLRP3 inflammatory pathway in the liver of rats after liver transplantation
Liver tissues from I/R group exhibited significant increase in the expression of TLR-4, MyD88, p-IKKα, p-IKKβ, p-IKK, p-IκBα, p-P65, NLRP3, ASC, Cleaved caspase-1, IL-1β, IL-18, TNF-α and IL-6 proteins compared to those in the sham group. As expected, pretreatment with salidroside (5, 10, or 20 mg/kg) reduced activation of the TLR-4/ NF-κB /NLRP3 inflammatory pathway (Fig. 3).
Figure 3.
Salidroside inhibits TLR-4/NF-κB/NLRP3 inflammatory pathway in vivo. (A,C) Representative western blot assays showing TLR-4/NF-κB/NLRP3 inflammatory pathway associated proteins in the rat liver after liver transplantation. (B,D) Results of the Western blot experiments. The statistical differences among groups were assessed by one-way ANOVA. nsP > 0.05, *P < 0.05, **P < 0.01, ***P < 0.001.
Salidroside mitigates hepatic IRI-induced inflammation and neutrophil infiltration
To establish a connection between neutrophil infiltration and liver inflammation, qRT-PCR was conducted to determine the expression levels of Pro-inflammatory cytokines and neutrophil markers, such as IL-1β, IL-18, IL-6, TNF-α, Ly6G and CD11b. Our analyses showed significantly elevated IL-1β, IL-18, IL-6 TNF-α, Ly6G and CD11b mRNA expression levels in the liver of the rats following liver transplantation, which were suppressed in the rats in the I/R + Sal (5, 10 or 20 mg/kg) group. The results of qRT-PCR indicated that salidroside pretreatment could mitigate hepatic IRI-induced inflammation and neutrophil infiltration in a dose-dependent manner (Fig. 4).
Figure 4.
Salidroside suppresses transcription of pro-inflammatory cytokinesis. (A) IL-1β mRNA expression. (B) IL-18 mRNA expression. (C) TNF-α mRNA expression. (D) IL-6 mRNA expression. (E) Ly6G mRNA expression. (F) CD11b mRNA expression. The statistical differences among groups were assessed by one-way ANOVA. nsP > 0.05, *P < 0.05, **P < 0.01, ***P < 0.001.
Salidroside induced macrophage M2 polarization and alleviates the H/R-induced inflammation through the TLR-4/NF-κB/NLRP3 inflammatory pathway
Notably, our data showed that H/R exposure elevates the TLR-4, MyD88, p-IKKα, p-IKKβ, p-IKK, p-IκBα, p-P65, NLRP3, ASC, Cleaved caspase-1, IL-1β, IL-18, TNF-α and IL-6 protein levels compared to those in the control group. Treatment with salidroside (1 μM, 10 μM or 50 μM) diminished the activation of TLR-4/NF-κB/NLRP3 inflammatory pathway and decreased the secretion of the proinflammatory factors in a dose-dependent manner. Although there were significantly higher levels of IL-1β, IL-18 and TNF-α in the cell supernatant of the H/R group, treatment with salidroside (1 M, 10 M, or 50 M) decreased the levels of these cytokines in a dose-dependent manner. Western blot analysis was used to determine the expression levels of M2 polarization-related proteins (Arg-1, CD206, IL-10). As the salidroside concentration increased, the M2 polarization effect of macrophage gradually increased (Fig. 5).
Figure 5.
Salidroside inhibits inflammation in the H/R-exposed macrophages by regulating TLR-4/NF-κB/NLRP3 inflammatory pathway. (A,C) Representative Western blot data showing TLR-4/NF-κB/NLRP3 inflammatory pathway associated proteins in macrophages. (B,D) The results of western blot experiments. (E) Expression of IL-1β, IL-18 and TNF-α in macrophages was analyzed by ELISA. (F) Expression of M2 polarization markers in macrophages was analyzed by western blot. The statistical differences among groups were assessed by one-way ANOVA. nsP > 0.05, *P < 0.05, **P < 0.01, ***P < 0.001.
Protective effect of salidroside is attenuated after TLR-4 activation
In comparison with the H/R + Sal (10 M) group, Western blotting analyses revealed that lipopolysaccharides (LPS) treatment significantly boosted the expression of TLR-4/NF-κB/NLRP3 inflammatory pathway related proteins (Fig. 6A–D). Similarly, compared to the H/R + Sal (10 μM) group, LPS significantly elevated the inflammatory cytokines in the cell supernatants (Fig. 6E). These data demonstrated that LPS (TLR-4 agonist) partly reversed the effects of salidroside. In addition, LPS stimulation significantly activated TLR-4/NF-κB/NLRP3 inflammatory pathway and facilitated the production of inflammatory cytokines by macrophages. Interestingly, the protective effects of salidroside in the macrophages with H/R exposure were attenuated after TLR-4 activation.
Figure 6.
LPS (TLR-4 activator) partially alleviates the anti-inflammatory ability of salidroside via regulation of the TLR-4/NF-κB/NLRP3 inflammatory pathway. (A,C) Representative Western blot data of the TLR-4/NF-κB/NLRP3 inflammatory pathway associated proteins in macrophages. (B,D) The results of western blot experiments. (E) Production of IL-1β, IL-18 and TNF-α in macrophages was assessed by ELISA. The statistical differences among groups were assessed by one-way ANOVA. nsP > 0.05, *P < 0.05, **P < 0.01, ***P < 0.001.
Discussion
Hepatic IRI caused by liver transplantation is one of the main causes of impaired liver function20. Increased ischemia time and enhanced liver inflammatory responses may result in a poorer prognosis and overall survival21. Although the etiology of hepatic IRI is complex, previous studies have demonstrated the important role of excessive inflammatory response in donor liver, which is one of the important factors leading to compromised liver functions22. Thus, pharmaceutical approaches targeting proinflammatory cytokines could lay the basis for development of hepatic IRI therapy.
Salidroside, one of the most active chemicals from Rhodiola plants, has been associated with remarkable biological activities, including anti-inflammatory, antioxidant, and hepatoprotective effects23–25. For instance, Gao et al. showed that salidroside reduces cartilage degradation by modulating inflammation and immunological responses through the NF-κB pathway26. Besides, Zheng and Yang demonstrated that salidroside improved hepatic lipid metabolism and activation of the NLRP3 inflammasome, ultimately alleviating nonalcoholic fatty liver disease27. However, the mechanism underlying the therapeutic effects of salidroside in the rat hepatic IRI following liver transplantation has not been fully investigated. Herein, we verified that salidroside improved liver function inhibit hepatocyte apoptosis, decreased the release of inflammatory cytokines in vitro, similarly suppressing inflammatory responses in vitro. Moreover, our studies suggested that salidroside exerts its hepatoprotective effects by inhibiting the inflammatory response through regulating the TLR-4/NF-κB/NLRP3 inflammatory pathway. Our results may provide some novel insights into the therapy of hepatic IRI.
In addition, our study showed that treatment with salidroside (5, 10 or 20 mg/kg) significantly decreased serum AST and ALT levels in rats after liver transplantation. We also demonstrated that salidroside treatment alleviated hepatic histopathological changes and inhibited hepatocyte apoptosis in the liver tissues of rats following liver transplantation, indicating the activities of salidroside in IRI-induced liver injury. Our findings agreed with previous studies which showed that salidroside confers hepatoprotective properties28.
Overproduction of inflammatory cytokines such as IL-1β, IL-18, IL-6, and TNF-α during the activation of IRI-induced immune responses is referred to as liver inflammation. Here, inflammatory substances accumulate in the liver and serum, aggravating endothelial cell damage and disrupting liver microcirculation through chemotaxis29,30. Our findings showed that salidroside alleviates hepatic IRI by suppressing the inflammatory responses. The inflammatory cytokines such as IL-1β, IL-18, IL-6, and TNF-α were shown to be overexpressed in both in vivo and in vitro hepatic IRI models. Furthermore, we showed that salidroside could inhibit the activation of the TLR-4/NF-B/NLRP3 inflammatory pathway in hepatic IRI, as well as the release of downstream inflammatory cytokines. The correlation between hepatic IRI and TLR-4/NF-κB signaling pathway has been reported. Hepatic IRI activates the TLR-4-mediated MyD88-dependent pathway and upregulates NF-κB which induces liver injury8,31. Besides, previous study has shown that damage-associated molecular pattern (DAMP) activates TLR-4 and MyD88, causing NF-κB to translocate to the nucleus via phosphorylation of the IκB at Ser32 and proteasome-mediated degradation32. The significance of TLR-4/NF-κB pathway in the activation of the NLRP3 inflammasome has already been reported33. Furthermore, NLRP3 promoted the recruitment of ASC, which then activated pro-caspase-1 into casepase-1, resulting in the production of mature IL-1β and IL-18, ultimately amplifying inflammatory responses and impairment34. The aberrant activation of the TLR-4/NF-κB/NLRP3 is quite significant in the formation and maintenance of the inflammatory microenvironment during hepatic IRI35. Our findings revealed that salidroside significantly reduces the expression of TLR-4, MyD88, p-IKKα, p-IKKβ, p-IKK, p-IκBα, p-P65, NLRP3, ASC, Cleaved caspase-1, IL-1β, IL-18, TNF-α and IL-6 in rats after liver transplantation as well as H/R-induced macrophages. Further analysis showed that salidroside reduces inflammation and hepatic IRI by inhibiting TLR-4-mediated NF-κB and inflammasome activation. Our data showed that TLR-4/NF-κB/NLRP3 inflammatory pathway was activated in rats after liver transplantation and in H/R induced macrophages. In addition, activation of the TLR-4/NF-κB/NLRP3 inflammatory pathway was inhibited by salidroside, and these effects were reversed by a TLR-4 agonist, suggesting that salidroside alleviate hepatic IRI by inhibiting the activation of TLR-4/NF-κB/NLRP3 inflammatory pathway and blocking TLR-4 (Fig. 7). Whereas our study highlights important findings, it is limited by the fact that we used a syngeneic liver transplantation mode to study liver transplantation IRI, which is not a perfect clinical model for studying allogeneic liver transplantation. Besides, we lacked clinical evidence to support the salidroside's effectiveness.
Figure 7.
Putative route by which salidroside attenuates inflammatory reactions in liver IRI. The mechanisms involved in salidroside inhibition of hepatic IRI-induced inflammatory response through the roles of TLR-4/MyD88/NF-κB and TLR-4/NF-κB/NLRP3 inflammatory pathway.
Conclusions
In conclusion, our data illustrated that salidroside is an anti-inflammatory compound and alleviates hepatic IRI by inhibiting TLR-4/NF-κB/NLRP3 inflammatory pathway. Thus, salidroside could be a novel therapeutic strategy in the treatment of hepatic IRI.
Supplementary Information
Abbreviations
- ALT
Alanine aminotransferase
- ASC
Apoptosis-associated speck-like protein
- AST
Aspartate aminotransferase
- DAPI
4,6-Diamidino-2-phenylindole
- MYD88
Myeloid differentiation factor 88
- HE
Hematoxylin–eosin
- H/R
Hypoxia/reoxygenation
- IL-1β
Interleukin-1β
- IL-6
Interleukin-6
- IL-18
Interleukin-18
- I/R
Ischemia/reperfusion
- IRI
Ischemia/reperfusion injury
- NF-κB
Nuclear factor kappa B
- NLRP3
NLR family pyrin domain-containing 3
- NLRs
Nucleotide-binding oligomerization domain-like receptors
- PRRs
Pattern recognition receptors
- SD
Sprague dawely
- TLR-4
Toll-like receptor 4
- TUNEL
Terminal deoxynucleotidyl transferase dUTP nick-end labeling
- TNF-α
Tumor necrosis factor-α
Author contributions
Y.L. and X.Q. designed the experiments and edited the final draft of this paper. Y.L., Z.L., H.C. and Q.K. performed the experiments.
Funding
This work was supported by the National Natural Science Foundation of Chongqing (No.cstc2020jcyj-msxmX0113).
Data availability
All data generated or analyzed during this study are included in this published article and supplementary material S1.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
These authors contributed equally: Yanyao Liu and Zilun Lei.
Supplementary Information
The online version contains supplementary material available at 10.1038/s41598-022-18369-4.
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Data Availability Statement
All data generated or analyzed during this study are included in this published article and supplementary material S1.