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关于咖啡、卡布奇诺和结缔组织生长因子——或者说如何保护你的肝脏!?

About coffee, cappuccino and connective tissue growth factor-Or how to protect your liver!?

机构信息

Institute of Clinical Chemistry and Pathobiochemistry, Central Laboratory, RWTH-University Hospital, Pauwelsstraße 30, 52074 Aachen, Germany.

出版信息

Environ Toxicol Pharmacol. 2009 Jul;28(1):1-10. doi: 10.1016/j.etap.2009.02.005. Epub 2009 Feb 21.

Abstract

Several epidemiological studies suggest that coffee drinking is inversely correlated with the risk of development of liver fibrosis. However, a causal, mechanistic explanation has long been pending. New results indicate that the methylxanthine caffeine, major component of coffee and the most widely consumed pharmacologically active substance in the world, might be responsible for this phenomenon as it, and even more potently its derived primary metabolite paraxanthine, inhibits transforming growth factor (TGF)-β-dependent and -independent synthesis of connective tissue growth factor (CTGF/CCN2) in liver parenchymal cells in vitro and in vivo. CTGF plays a crucial role in the fibrotic remodeling of various organs which has therefore frequently been proposed as therapeutic target in the management of fibrotic disorders. This article summarizes the clinical-epidemiological observations as well as the pathophysiological background of the antifibrotic effects of coffee consumption and provides suggestions for the therapeutic use of caffeine and its derived metabolic methylxanthines as potentially powerful drugs in patients with chronic fibrogenic liver disease by their inhibitory effect on (hepatocellular) CTGF synthesis.

摘要

多项流行病学研究表明,喝咖啡与肝纤维化发展的风险呈负相关。然而,长期以来,其因果机制尚未得到明确解释。新的研究结果表明,甲基黄嘌呤咖啡因(咖啡的主要成分,也是世界上应用最广泛的具有药理活性的物质)可能是导致这种现象的原因,因为它,甚至其衍生的初级代谢物 1,7-二甲基黄嘌呤,能抑制转化生长因子(TGF)-β依赖性和非依赖性的细胞外基质生长因子(CTGF/CCN2)在肝实质细胞中的合成,无论是在体外还是在体内。CTGF 在各种器官的纤维化重塑中起着至关重要的作用,因此经常被提议作为纤维化疾病治疗的靶点。本文总结了咖啡摄入的抗纤维化作用的临床流行病学观察和病理生理学背景,并提出了通过抑制(肝细胞)CTGF 合成,将咖啡因及其衍生的代谢甲基黄嘌呤作为潜在的强力药物,用于治疗慢性纤维性肝病患者的治疗建议。

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