Selvakumar Elangovan, Prahalathan Chidambaram, Mythili Yenjerla, Varalakshmi Palaninathan
Department of Medical Biochemistry, Dr A.L.M. Post Graduate Institute of Basic Medical Sciences, University of Madras, Taramani Campus, Chennai, India.
Mol Cell Biochem. 2005 Apr;272(1-2):179-85. doi: 10.1007/s11010-005-7322-4.
The present study investigated the protective effect of DL-alpha-lipoic acid on the tissue peroxidative damage and abnormal antioxidant levels in cyclophosphamide (CP) induced hepatotoxicity. Male Wistar rats of 140 +/- 20 g were categorized into four groups. Two groups were administered CP (15 mg/kg body weight once a week for 10 weeks by oral gavage) to induce hepatotoxicity; one of these groups received lipoic acid treatment (35 mg/kg body weight intraperitoneally once a week for 10 weeks; 24 h prior to the CP administration). A vehicle (saline) treated control group and a lipoic acid drug control group were also included. The extent of liver damage in CP-induced rats was evident from the increased activities of serum aminotransferases, alkaline phosphatase and lactate dehydrogenase; whereas lipoic acid pretreatment prevented the rise in these marker enzymes. We evaluated the changes in activities/levels of tissue enzymic (superoxide dismutase, catalase, glutathione peroxidase, glutathione-S-transferase, glutathione reductase and glucose-6-phosphate dehydrogenase) and non-enzymic (reduced glutathione, ascorbate and a-tocopherol) antioxidants along with malondialdehyde levels in the experimental groups. In CP-administered rats the antioxidant enzymes showed significantly depressed activities (p < 0.001, p < 0.01) and the antioxidant molecules also showed depleted levels (p < 0.001, p < 0.01), in comparison with the control group. However the extent of lipid peroxidation and the abnormal antioxidant status were normalized in lipoic acid pretreated rats. The present work highlights the efficacy of lipoic acid as a cytoprotectant in CP-induced hepatic oxidative injury.
本研究调查了DL-α-硫辛酸对环磷酰胺(CP)诱导的肝毒性中组织过氧化损伤和异常抗氧化水平的保护作用。将体重140±20 g的雄性Wistar大鼠分为四组。两组给予CP(每周一次口服灌胃15 mg/kg体重,共10周)以诱导肝毒性;其中一组接受硫辛酸治疗(每周一次腹腔注射35 mg/kg体重,共10周;在给予CP前24小时)。还包括一个溶剂(生理盐水)处理的对照组和一个硫辛酸药物对照组。CP诱导的大鼠肝脏损伤程度可从血清氨基转移酶、碱性磷酸酶和乳酸脱氢酶活性增加看出;而硫辛酸预处理可防止这些标志物酶的升高。我们评估了实验组中组织酶促抗氧化剂(超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽-S-转移酶、谷胱甘肽还原酶和葡萄糖-6-磷酸脱氢酶)和非酶促抗氧化剂(还原型谷胱甘肽、抗坏血酸和α-生育酚)的活性/水平变化以及丙二醛水平。与对照组相比,给予CP的大鼠抗氧化酶活性显著降低(p<0.001,p<0.01),抗氧化分子水平也降低(p<0.001,p<0.01)。然而,硫辛酸预处理的大鼠脂质过氧化程度和异常抗氧化状态恢复正常。本研究突出了硫辛酸辛酸酸作为CP诱导的肝脏氧化损伤细胞保护剂的功效。