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肝毒性机制。I. 肿瘤坏死因子诱导的肝损伤。

Mechanisms of hepatic toxicity. I. TNF-induced liver injury.

作者信息

Bradham C A, Plümpe J, Manns M P, Brenner D A, Trautwein C

机构信息

Department of Medicine, University of North Carolina, Chapel Hill, North Carolina 27599-7080, USA.

出版信息

Am J Physiol. 1998 Sep;275(3):G387-92. doi: 10.1152/ajpgi.1998.275.3.G387.

Abstract

Tumor necrosis factor-alpha (TNF-alpha) functions as a two-edged sword in the liver. TNF-alpha is required for normal hepatocyte proliferation during liver regeneration. It functions both as a comitogen and to induce the transcription factor nuclear factor-kappaB, which has antiapoptotic effects. On the other hand, TNF-alpha is the mediator of hepatotoxicity in many animal models, including those involving the toxins concanavalin A and lipopolysaccharide. TNF-alpha has also been implicated as an important pathogenic mediator in patients with alcoholic liver disease and viral hepatitis.

摘要

肿瘤坏死因子-α(TNF-α)在肝脏中起着双刃剑的作用。肝脏再生过程中正常肝细胞增殖需要TNF-α。它既作为一种协同有丝分裂原发挥作用,又能诱导具有抗凋亡作用的转录因子核因子-κB。另一方面,在许多动物模型中,包括那些涉及伴刀豆球蛋白A和脂多糖毒素的模型,TNF-α是肝毒性的介质。在酒精性肝病和病毒性肝炎患者中,TNF-α也被认为是一种重要的致病介质。

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