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首页> 外文期刊>Bulletin of experimental biology and medicine >Pathways of Apoptosis Regulation in Hepatocytes Induced by First-Line Antitubercular Drugs
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Pathways of Apoptosis Regulation in Hepatocytes Induced by First-Line Antitubercular Drugs

机译:一线抗细胞药物诱导肝细胞凋亡调控的途径

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摘要

We studied pathways of apoptosis regulation during experimental hepatopathy caused by treatment with antitubercular drugs and involvement of some hepatoprotectors and immunomodulators in the regulation of hepatocyte apoptosis induced by antitubercular drugs. The intensity of apoptosis and expression of apoptosis-associated molecules were evaluated. It was shown that antitubercular drugs induce apoptosis in hepatocytes by triggering external signaling pathway and p53-dependent signaling pathway and simultaneously reducing the level of anti-apoptotic Bcl-2 protein. Runihol, remaxol, and cycloferon reduced degenerative effects in the liver, though the level of apoptosis remained high. Ademetionine in tablets and reamberin improved the microstructure of the liver by inhibiting both apoptotic pathways induced by the antitubercular drugs; in other words, they have distinct hepatoprotective and apoptosis-protective effects, which is especially important at the late stages of ontogeny.
机译:我们研究了通过治疗抗细胞药物治疗和一些肝脏保护剂和免疫调节剂在抗伞菌药物诱导肝细胞凋亡调控中引起的实验性肝病期间研究了凋亡调节的途径。 评估凋亡和凋亡相关分子的表达的强度。 结果表明,通过触发外部信号通路和P53依赖的信号通路并同时降低抗凋亡Bcl-2蛋白水平来诱导肝细胞凋亡凋亡。 Runihol,Remaxol和Cycloferon降低了肝脏的退行性效果,尽管细胞凋亡水平仍然很高。 通过抑制抗细胞药物诱导的凋亡途径来改善平板电脑和雷米蛋白的Ademetionine改善了肝脏的微观结构; 换句话说,它们具有不同的肝保护和凋亡保护作用,这在组来生成的晚期尤为重要。

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