Capsaicin alleviates acetaminophen-induced acute liver injury in mice

被引:28
作者
Zhan, Xiang [1 ]
Zhang, Jianqiang [1 ,3 ]
Chen, Hui [1 ]
Liu, Liyuan [1 ]
Zhou, Yiming [1 ]
Zheng, Ting [1 ]
Li, Suxiao [1 ]
Zhang, Yanxiang [1 ]
Zheng, Bing [1 ,2 ]
Gong, Quan [1 ,2 ]
机构
[1] Yangtze Univ, Sch Med, Dept Immunol, Jingzhou, Peoples R China
[2] Yangtze Univ, Clin Mol Immunol Ctr, Sch Med, Jingzhou, Peoples R China
[3] Ezhou Cent Hosp, Dept Nephrol, Ezhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Capsaicin; Acetaminophen; Acute liver injury; HMGB1/TLR4/NF-kappa B signaling pathway; Apoptosis; Inflammation; HEPATIC-INJURY; BCL-2; ACTIVATION; HEPATOTOXICITY; APOPTOSIS; BAX;
D O I
10.1016/j.clim.2020.108578
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Overdose of N-acetyl-para-aminophenol (APAP) can induce acute liver injury (ALI). We evaluated the potential protective effect of 8-methyl-N-geranyl-6-nonamide (capsaicin (CAP)) in APAP-induced ALI in mice. ALI was induced by APAP (150 mg/kg, i.p.) administration; CAP pretreatment (1 mg/kg) was undertaken before APAP injection for 3 consecutive days. We found that CAP pretreatment attenuated ALI significantly; improve the oxidative stress-associated indicators (hepatic expression of malondialdehyde (MDA) superoxide dismutase (SOD) and glutathione (GSH)); downregulate expression of proinflammatory cytokines (interleukin (IL)-6, IL-1 beta, tumor necrosis factor-alpha) through the high-mobility group box 1/toll-like receptor-4/nuclear factor-kappa B (HMGB1/TLR4/NF-kappa B) signaling pathway; alleviate hepatocyte apoptosis by inhibiting expression of B-cell lymphoma-2-associated X, caspase-3 and cleaved caspase-3. CAP pretreatment reduced expression of B-cell lymphoma-2, which served as a hepatotoxic factor rather than an anti-apoptotic protein in our mouse model. We propose that CAP can alleviate APAP-induced ALI by inhibiting the inflammatory response, attenuating oxidative stress, and reducing hepatocyte apoptosis.
引用
收藏
页数:9
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