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蒌叶对D-半乳糖胺诱导的肝毒性大鼠肝脏标志物酶及组织抗氧化状态的影响。

Influence of Piper betle on hepatic marker enzymes and tissue antioxidant status in D-galactosamine-induced hepatotoxic rats.

作者信息

Pushpavalli Ganesan, Veeramani Chinnadurai, Pugalendi Kodukkur Viswanathan

机构信息

Department of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Annamalainagar 608 002, Tamilnadu, India.

出版信息

J Basic Clin Physiol Pharmacol. 2008;19(2):131-50. doi: 10.1515/jbcpp.2008.19.2.131.

DOI:10.1515/jbcpp.2008.19.2.131
PMID:19024930
Abstract

D-galactosamine is a well-established hepatotoxicant that induces a diffuse type of liver injury closely resembling human viral hepatitis. D-galactosamine by its property of generating free radicals causes severe damage to the membrane and affects almost all organs of the human body. The leaves of Piper betle L., a commonly used masticatory in Asian countries, possess several biological properties. Our aim is to investigate the in vivo antioxidant potential of P. betle leaf-extract against oxidative stress induced by D-galactosamine intoxication in male albino Wistar rats. Toxicity was induced by an intraperitoneal injection of D-galactosamine, 400 mg/kg body weight (BW) for 21 days. Rats were treated with P. betle extract (200 mg/kg BW) via intragastric intubations. We assessed the activities of liver marker enzymes (aspartate amino-transferase, alanine aminotransferase, alkaline phosphatase, gamma glutamyl transpeptidase) and levels of thiobarbituric acid reactive substances (TBARS), lipid hydroperoxides, superoxide dismutase, catalase, glutathione peroxidase, vitamin C, vitamin E, and reduced glutathione. The extract significantly improved the status of antioxidants and decreased TBARS, hydroperoxides, and liver marker enzymes when compared with the D-galactosamine treated group, demonstrating its hepatoprotective and antioxidant properties.

摘要

D-半乳糖胺是一种公认的肝毒性物质,可引发一种与人类病毒性肝炎极为相似的弥漫性肝损伤。D-半乳糖胺因其产生自由基的特性,会对细胞膜造成严重损伤,并影响人体几乎所有器官。蒌叶是亚洲国家常用的一种咀嚼物,其叶子具有多种生物学特性。我们的目的是研究蒌叶提取物对雄性白化Wistar大鼠因D-半乳糖胺中毒诱导的氧化应激的体内抗氧化潜力。通过腹腔注射400mg/kg体重的D-半乳糖胺,持续21天来诱导毒性。通过胃内插管给大鼠喂食蒌叶提取物(200mg/kg体重)。我们评估了肝脏标记酶(天冬氨酸氨基转移酶、丙氨酸氨基转移酶、碱性磷酸酶、γ-谷氨酰转肽酶)的活性以及硫代巴比妥酸反应性物质(TBARS)、脂质氢过氧化物、超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、维生素C、维生素E和还原型谷胱甘肽的水平。与D-半乳糖胺处理组相比,该提取物显著改善了抗氧化剂的状态,并降低了TBARS、氢过氧化物和肝脏标记酶的水平,证明了其肝脏保护和抗氧化特性。

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