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An Overview of the Mechanism of Penthorum chinense Pursh on Alcoholic Fatty Liver

机译:五旬节中国富含酒精脂肪肝的机制概述

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Alcohol liver disease (ALD) caused by excessive alcohol consumption is a progressive disease, and alcohol fatty liver disease is the primary stage. Currently, there is no approved drug for its treatment. Abstinence is the best way to heal, but patients’ compliance is poor. Unlike other chronic diseases, alcohol fatty liver disease is not caused by nutritional deficiencies; it is caused by the molecular action of ingested alcohol and its metabolites. More and more studies have shown the potential of Penthorum chinense Pursh (PCP) in the clinical use of alcohol fatty liver treatment. The purpose of this paper is to reveal from the essence of PCP treatment of alcohol liver mechanism mainly by the ethanol dehydrogenase (ADH) and microsomal ethanol oxidation system-dependent cytochrome P4502E1 (CYP2E1) to exert antilipogenesis, antioxidant, anti-inflammatory, antiapoptotic, and autophagy effects, with special emphasis on its mechanisms related to SIRT1/AMPK, KEAP-1/Nrf2, and TLR4/NF-κB. Overall, data from the literature shows that PCP appears to be a promising hepatoprotective traditional Chinese medicine (TCM).
机译:由过量饮酒引起的酒精肝病(ALD)是一种渐进性疾病,酒精脂肪肝病是初级阶段。目前,没有批准的药物治疗。禁欲是愈合的最佳方式,但患者的遵守性很差。与其他慢性疾病不同,酒精脂肪肝病不是由营养缺陷引起的;它是由摄入醇及其代谢物的分子作用引起的。越来越多的研究表明,在临床使用酒精脂肪肝治疗中的Penthorum Chinenst Pursh(PCP)的潜力。本文的目的是揭示从酒精肝脏机制的PCP治疗的本质主要由乙醇脱氢酶(ADH)和微粒体乙醇氧化系统依赖性细胞色素P4502E1(CYP2E1)施加抗氧化发生,抗氧化剂,抗炎,抗透露性,和自噬效果,特别强调其与SIRT1 / AMPK,Keap-1 / NRF2和TLR4 / NF-κB相关的机制。总体而言,文献中的数据表明,PCP似乎是一种有前途的肝保护性中药(TCM)。

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