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通过改善对乙酰氨基酚挑战大鼠的线粒体氧化应激,DL-α-硫辛酸和α-生育酚的肝保护作用。

Hepatoprotective effects of DL-α-lipoic acid and α-Tocopherol through amelioration of the mitochondrial oxidative stress in acetaminophen challenged rats.

机构信息

Department of Microbiology, Amala Cancer Research Centre, Thrissur, Kerala, India.

出版信息

Toxicol Mech Methods. 2013 Jun;23(5):368-76. doi: 10.3109/15376516.2013.769289. Epub 2013 Apr 23.

DOI:10.3109/15376516.2013.769289
PMID:23343353
Abstract

Acetaminophen (APAP) is known to induce liver mitochondrial dysfunction leading to acute hepatotoxicity. Effect of DL-α-lipoic acid (LA) and α-tocopherol (α-Toc) against the APAP-induced liver mitochondrial damage was evaluated in rats. LA (100 mg/kg, p.o.) and α-Toc (100 mg/kg, p.o.) were given once daily for 15 d, prior to the APAP administration (3 g/kg, p.o). Hepatic damage was confirmed by determining the activities of serum glutamate pyruvate transaminase, serum glutamate oxaloacetate transaminase and alkaline phosphatase, 4 h after the single dose of APAP. To assess the mitochondrial damage, the activities of antioxidant enzymes, Krebs' cycle dehydrogenases and mitochondrial electron transport chain complexes, and levels of reactive oxygen species (ROS), reduced glutathione, lipid peroxidation (malondialdehyde, MDA) as well as the mitochondrial membrane potential (Δψmt) were evaluated. The activities of mitochondrial enzymes and Δψmt were significantly (p < 0.01) decreased and the level of ROS and MDA were significantly (p < 0.01) increased due to APAP challenge. LA and α-Toc treatment significantly enhanced the activities of mitochondrial enzymes and Δψmt than that of control group; whereas the levels of ROS and MDA were decreased. The results of the study concluded that the liver damage induced by APAP was significantly ameliorated by LA and α-Toc. LA showed more protection than that of α-Toc. The protection can be partially ascribed to their mitochondrial protective effects through their antioxidant activity which could decrease the level of ROS and by direct enhancement of Δψmt.

摘要

醋氨酚(APAP)已知可诱导肝线粒体功能障碍导致急性肝毒性。在大鼠中评价了 DL-α-硫辛酸(LA)和α-生育酚(α-Toc)对 APAP 诱导的肝线粒体损伤的作用。LA(100mg/kg,po)和α-Toc(100mg/kg,po)在单次 APAP 给药(3g/kg,po)前每天给予一次,共 15 天。单次 APAP 给药后 4 小时通过测定血清谷氨酸丙酮酸转氨酶、血清谷氨酸草酰乙酸转氨酶和碱性磷酸酶的活性来确认肝损伤。为了评估线粒体损伤,评估了抗氧化酶、克雷布斯循环脱氢酶和线粒体电子传递链复合物的活性以及活性氧(ROS)、还原型谷胱甘肽、脂质过氧化(丙二醛,MDA)和线粒体膜电位(Δψmt)的水平。由于 APAP 挑战,线粒体酶的活性和Δψmt显著(p<0.01)降低,而 ROS 和 MDA 的水平显著(p<0.01)增加。LA 和α-Toc 处理显著提高了线粒体酶的活性和Δψmt比对照组;而 ROS 和 MDA 的水平降低。研究结果表明,LA 和α-Toc 显著改善了 APAP 引起的肝损伤。LA 的保护作用比α-Toc 更强。这种保护作用部分归因于它们的抗氧化活性,通过降低 ROS 水平和直接增强Δψmt,发挥线粒体保护作用。

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