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[脂氧合酶抑制剂在原代培养中诱导大鼠肝细胞凋亡]

[Lipoxygenase inhibitors induce rat hepatocyte apoptosis in primary culture].

作者信息

Korniĭchuk H M, Makohon N V, Lushnikova I V, Aleksieieva I M

机构信息

Bogomolets Institute of Physiology, National Academy of Sciences of Ukraine, Kyiv.

出版信息

Ukr Biokhim Zh (1999). 2002 Jan-Feb;74(1):125-7.

Abstract

Arachidonic acid metabolites have been shown to have a wide range of effects on cell proliferation and viability. In this study, the effects of lipoxygenase (LO) inhibitors nordihydroguaiaretic acid (NDGA) and caffeic acid (CA) on the viability of cultured rat hepatocytes (HC) were investigated. As a result, treatment with NDGA and CA for 4 h and 24 h decreased ALT release from HC and increased a number of apoptotic cells. Apoptosis inducing effects of general LO inhibitor NDGA were more pronounced, than those of 5-LO inhibitor CA. The results suggest that lipoxygenase pathway of arachidonic acid metabolism, in particular 5-LO, is essential regulator of hepatocyte survival and apoptosis.

摘要

花生四烯酸代谢产物已被证明对细胞增殖和活力具有广泛影响。在本研究中,研究了脂氧合酶(LO)抑制剂去甲二氢愈创木酸(NDGA)和咖啡酸(CA)对培养的大鼠肝细胞(HC)活力的影响。结果,用NDGA和CA处理4小时和24小时可减少HC中ALT的释放,并增加凋亡细胞的数量。一般LO抑制剂NDGA的凋亡诱导作用比5-LO抑制剂CA更明显。结果表明,花生四烯酸代谢的脂氧合酶途径,尤其是5-LO,是肝细胞存活和凋亡的重要调节因子。

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