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对乙酰氨基酚肝毒性机理及药物干预靶点 被引量:36
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作者 汪倩 徐瑞娟 杨劲 《药学与临床研究》 2011年第3期247-252,共6页
由于对乙酰氨基酚用药普遍性和广泛性,其肝毒性问题日益引起人们的关注。本文介绍对乙酰氨基酚肝脏代谢、转运以及与Keap1-Nrf2通路有关的生理性调控机制,阐述对乙酰氨基酚的肝毒性机理,包括代谢损伤和氧化应激损伤两大理论。并以此为... 由于对乙酰氨基酚用药普遍性和广泛性,其肝毒性问题日益引起人们的关注。本文介绍对乙酰氨基酚肝脏代谢、转运以及与Keap1-Nrf2通路有关的生理性调控机制,阐述对乙酰氨基酚的肝毒性机理,包括代谢损伤和氧化应激损伤两大理论。并以此为基础从吸收、代谢、转运等方面对其治疗靶点及干预药物加以综述。其中,Keap1-Nrf2抗氧化解毒通路和转运蛋白环节与对乙酰氨基酚肝毒性关系的研究在近几年逐渐增多,有望发现新的治疗靶点和对乙酰氨基酚肝毒性的有效治疗药物。 展开更多
关键词 对乙酰氨基酚肝毒性 代谢损伤 氧化应激 Keap1-Nrf2通路
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Protective effect of Sharbat-e-Deenar against acetaminophen-induced hepatotoxicity in experimental animals
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作者 Arvind Kumar Shakya Sangeeta Shukla 《Journal of Traditional Chinese Medicine》 SCIE CAS CSCD 2017年第3期387-392,共6页
OBJECTIVE: To investigate the effect of Sharbat-e-Deenar(SD) on acetaminophen(APAP)-induced hepatotoxicity in rat model.METHODS: Albino rats were treated with SD at the doses of 1, 2 and 4 mL/kg, p.o. against hepatoto... OBJECTIVE: To investigate the effect of Sharbat-e-Deenar(SD) on acetaminophen(APAP)-induced hepatotoxicity in rat model.METHODS: Albino rats were treated with SD at the doses of 1, 2 and 4 mL/kg, p.o. against hepatotoxicity after APAP(2 g/kg, p.o. once only) intoxication.The blood, tissue biochemical parameters and histopathological observation were performed. The RESULTS: APAP exposure in rats significantly increased the level of biochemical parameters such as aspartate aminotransaminase, alanine aminotransaminase, lactate dehydrogenase, serum alkaline phosphatase, bilirubin, urea and creatinine into blood circulation which were reversed towards normal by SD therapy at all doses. The tissue biochemical parameters such as lipid peroxidation, reduced glutathione, adenosine tri-phosphatase and glucose-6-phosphatase were significantly restored after SD treatment against hepatotoxity. Histological analysis confirmed that SD-treated rats significantly alleviated of liver damage and reduced lesions caused by APAP intoxication. The biochemical changes are in good correlation with the histopathological observations.CONCLUSION: On the basis of these results, it can be concluded that SD exerts hepatoprotective activity against APAP-induced liver injury. 展开更多
关键词 Sharbat-e-Deenar ACETAMINOPHEN Hepatitis toxic HEPATOPROTECTION
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