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ME3738通过一种依赖白细胞介素-6的机制预防伴刀豆球蛋白A诱导的肝衰竭。

ME3738 protects from concanavalin A-induced liver failure via an IL-6-dependent mechanism.

作者信息

Klein Christian, Wüstefeld Torsten, Heinrich Peter C, Streetz Konrad L, Manns Michael P, Trautwein Christian

机构信息

Department of Gastroenterology, Hepatology and Endocrinology, Medizinische Hochschule Hannover, Hannover, Germany.

出版信息

Eur J Immunol. 2003 Aug;33(8):2251-61. doi: 10.1002/eji.200323651.

Abstract

ME3738 is a new compound that attenuates liver disease in several models of acute and chronic liver inflammation. We used the concanavalin A (Con A) model to elucidate the molecular mechanisms of ME3738 to block liver cell damage. Pretreatment of BALB/c mice with ME3738 prior to Con A injection resulted in a significant reduction in liver injury. The protective effect of ME3738 prior to Con A injection was associated with a reduction in IL-6 serum levels and NF-kappaB DNA binding in liver nuclear extracts. However, STAT3 DNA binding was induced via ME3738 prior to Con A injection. Further analysis showed that ME3738 induces IL-6 serum levels and activates STAT3 DNA binding and target gene transcription. The relevance of this finding was assessed in IL-6(-/-) mice. In these animals, ME3738 induced no increase in IL-6 serum expression, and activation of IL-6-dependent pathways was not found. In addition, ME3738 did not protect IL-6(-/-) animals from Con A-induced liver failure, while IL-6 injection was still effective. Therefore, we demonstrate that ME3738 triggers IL-6 expression, which activates pathways that are relevant to protect from Con A-induced liver failure.

摘要

ME3738是一种新型化合物,在多种急性和慢性肝脏炎症模型中可减轻肝脏疾病。我们使用刀豆蛋白A(Con A)模型来阐明ME3738阻断肝细胞损伤的分子机制。在注射Con A之前用ME3738预处理BALB/c小鼠,可使肝损伤显著减轻。Con A注射前ME3738的保护作用与血清IL-6水平降低以及肝核提取物中NF-κB DNA结合减少有关。然而,在Con A注射前,ME3738可诱导STAT3 DNA结合。进一步分析表明,ME3738可诱导血清IL-6水平升高,并激活STAT3 DNA结合及靶基因转录。在IL-6基因敲除(IL-6(-/-))小鼠中评估了这一发现的相关性。在这些动物中,ME3738未诱导血清IL-6表达增加,也未发现IL-6依赖途径的激活。此外,ME3738不能保护IL-6(-/-)动物免受Con A诱导的肝衰竭,而注射IL-6仍然有效。因此,我们证明ME3738触发IL-6表达,从而激活与保护免受Con A诱导的肝衰竭相关的途径。

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