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大蒜及其衍生物S-烯丙基半胱氨酸通过激活Wistar大鼠肝细胞中的Nrf2,降低了六价铬诱导的氧化应激和细胞凋亡。

Chromium (VI)-induced oxidative stress and apoptosis is reduced by garlic and its derivative S-allylcysteine through the activation of Nrf2 in the hepatocytes of Wistar rats.

作者信息

Kalayarasan Srinivasan, Sriram Narayanan, Sureshkumar Ananthasadagopan, Sudhandiran Ganapasam

机构信息

Department of Biochemistry, University of Madras, Guindy campus, Chennai-600 025, India.

出版信息

J Appl Toxicol. 2008 Oct;28(7):908-19. doi: 10.1002/jat.1355.

Abstract

Chromium (VI) compounds are genotoxic and carcinogenic in a variety of experimental systems. Garlic and its derivatives possess antioxidant properties to scavenge the toxic radicals. The mechanism by which garlic induces the antioxidant and phase II enzymes during oxidative stress-induced apoptosis is not known. This study aims to evaluate the protective role of aqueous garlic extract (AGE; 200 mg kg(-1) b.w.) and S-allylcysteine (SAC; 100 mg kg(-1) b.w.) on potassium dichromate-induced apoptosis and oxidative stress in the hepatocytes of Wistar rats. Activities of liver marker enzymes such as aspartate transaminase, alanine transaminase and lactate dehydrogenase were found to be increased in the serum of chromium-induced group, whereas administration of garlic extract and SAC restored the enzymes to near normal status. The activities of enzymic antioxidants (superoxide dismutase, catalase, glutathione peroxidase), non-enzymic antioxidants (vitamin C and vitamin E) and the levels of reduced glutathione were found to be decreased, while an increase in lipid peroxidation (LPO) and reactive oxygen species were observed in the liver tissues of chromium-induced group. Administration of AGE and SAC reversed the status of these parameters substantially. Histological and transmission electron microscopic studies support our findings. Confocal microscopic analysis using annexin-V showed the involvement of apoptosis. Further, the expression of a novel transcription factor, nuclear factor-E2 related factor 2 (Nrf2) was investigated using Immunofluorescence and Western blotting. The results show the promising role of Nrf2-mediated antioxidant defense of AGE and SAC against chromium toxicity.

摘要

六价铬化合物在多种实验系统中具有基因毒性和致癌性。大蒜及其衍生物具有抗氧化特性,可清除有毒自由基。大蒜在氧化应激诱导的细胞凋亡过程中诱导抗氧化酶和二期酶的机制尚不清楚。本研究旨在评估大蒜水提取物(AGE;200毫克/千克体重)和S-烯丙基半胱氨酸(SAC;100毫克/千克体重)对重铬酸钾诱导的Wistar大鼠肝细胞凋亡和氧化应激的保护作用。在铬诱导组的血清中,发现肝标志物酶如天冬氨酸转氨酶、丙氨酸转氨酶和乳酸脱氢酶的活性增加,而给予大蒜提取物和SAC可使这些酶恢复到接近正常水平。在铬诱导组的肝组织中,发现酶促抗氧化剂(超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶)、非酶促抗氧化剂(维生素C和维生素E)的活性以及还原型谷胱甘肽水平降低,同时观察到脂质过氧化(LPO)和活性氧增加。给予AGE和SAC可使这些参数的状态显著逆转。组织学和透射电子显微镜研究支持我们的发现。使用膜联蛋白-V的共聚焦显微镜分析显示细胞凋亡的参与。此外,使用免疫荧光和蛋白质印迹法研究了一种新型转录因子核因子E2相关因子2(Nrf2)的表达。结果显示Nrf2介导的AGE和SAC抗氧化防御对铬毒性具有显著作用。

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