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六种五味子木脂素对乙酰氨基酚诱导的肝损伤的肝保护作用部分与抑制细胞色素P450介导的生物活化有关。

Hepato-protective effects of six schisandra lignans on acetaminophen-induced liver injury are partially associated with the inhibition of CYP-mediated bioactivation.

作者信息

Jiang Yiming, Fan Xiaomei, Wang Ying, Tan Huasen, Chen Pan, Zeng Hang, Huang Min, Bi Huichang

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.

The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

出版信息

Chem Biol Interact. 2015 Apr 25;231:83-9. doi: 10.1016/j.cbi.2015.02.022. Epub 2015 Mar 6.

Abstract

Acetaminophen (APAP) overdose is the most frequent cause of drug-induced acute liver failure. Schisandra fructus is widely-used traditional Chinese medicine which possesses hepato-protective potential. Schisandrin A (SinA), Schisandrin B (SinB), Schisandrin C (SinC), Schisandrol A (SolA), Schisandrol B (SolB), and Schisantherin A (SthA) are the major bioactive lignans. Most recently, we found SolB exerts significant hepato-protection against APAP-induced liver injury. In this study, the protective effects of the other five schisandra lignans against APAP-induced acute hepatotoxicity in mice were investigated and compared with that of SolB. The results of morphological and biochemical assessment clearly demonstrated significant protective effects of SinA, SinB, SinC, SolA, SolB, and SthA against APAP-induced liver injury. Among these schisandra lignans, SinC and SolB exerted the strongest hepato-protective effects against APAP-induced hepatotoxicity. Six lignans pretreatment before APAP dosing could prevent the depletions of total liver glutathione (GSH) and mitochondrial GSH caused by APAP. Additionally, the lignans treatment inhibited the enzymatic activities of three CYP450 isoforms (CYP2E1, CYP1A2, and CYP3A11) related to APAP bioactivation, and further decreased the formation of APAP toxic intermediate N-acetyl-p-benzoquinone imine (NAPQI) in mouse microsomal incubation system. This study demonstrated that SinA, SinB, SinC, SolA, SolB and SthA exhibited significant protective actions toward APAP-induced liver injury, which was partially associated with the inhibition of CYP-mediated APAP bioactivation.

摘要

对乙酰氨基酚(APAP)过量是药物性急性肝衰竭最常见的原因。五味子是一种具有肝脏保护潜力的广泛使用的传统中药。五味子甲素(SinA)、五味子乙素(SinB)、五味子丙素(SinC)、五味子醇甲(SolA)、五味子醇乙(SolB)和五味子酯甲(SthA)是主要的生物活性木脂素。最近,我们发现SolB对APAP诱导的肝损伤具有显著的肝脏保护作用。在本研究中,研究了其他五种五味子木脂素对APAP诱导的小鼠急性肝毒性的保护作用,并与SolB进行了比较。形态学和生化评估结果清楚地表明,SinA、SinB、SinC、SolA、SolB和SthA对APAP诱导的肝损伤具有显著的保护作用。在这些五味子木脂素中,SinC和SolB对APAP诱导的肝毒性具有最强的肝脏保护作用。在给予APAP之前进行六种木脂素预处理可以防止APAP引起的肝脏总谷胱甘肽(GSH)和线粒体GSH的消耗。此外,木脂素处理抑制了与APAP生物活化相关的三种细胞色素P450同工酶(CYP2E1、CYP1A2和CYP3A11)的酶活性,并进一步减少了小鼠微粒体孵育系统中APAP毒性中间体N-乙酰-p-苯醌亚胺(NAPQI)的形成。本研究表明,SinA、SinB、SinC、SolA、SolB和SthA对APAP诱导的肝损伤具有显著的保护作用,这部分与抑制CYP介导的APAP生物活化有关。

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