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The PERK/eIF2 alpha/ATF4/CHOP pathway plays a role in regulating monocrotaline-induced endoplasmic reticulum stress in rat liver

机译:Perk / EIF2α/ ATF4 / Chop路径在调节大鼠肝脏中的偏分法诱导的内质网胁迫方面发挥作用

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Monocrotaline (MCT) belongs to the category of Pyrrolizdine Alkaloids (PAs), which is one of important hepatotoxic alkaloid in Crotalaria Lin. Apoptosis is one mechanism of toxic responses induced by MCT. However, the underlying mechanism of liver apoptosis caused by MCT through Endoplasmic reticulum (ER) stress continues to be incompletely understood. In this study, we describe the role of ER stress in MCT induced hepato-toxicity in rats. 24 male rats were randomly divided into 3 groups: normal saline group, 45 mg/kg MCT group and 90 mg/kg MCT group. After 48 h of saline/MCT administration, the livers were collected for analysis of ER stress-related proteins by Western blotting. The expression of GRP78, p-IRE1 alpha, ATF6 and caspase-12 showed a dose-dependent increase. PERK/eIF2 alpha/ATF4/CHOP pathway is one of the major ER stress pathways which is required for cell survival. Therefore, through analyzing the effects of MCT on this pathway, we found the protein levels of p-PERK, p-eIF2 alpha, ATF4 and CHOP were increase obviously. All these results indicate that MCT induces ER stress in rat liver. The PERK/eIF2 alpha/ATF4/CHOP pathway is involved in the regulation of MCT-induced ER stress in the liver of rat.
机译:龙罗素碱(MCT)属于吡咯粒子生物碱(PAS)的类别,这是克罗塔利亚林的重要肝毒性生物碱之一。细胞凋亡是MCT诱导有毒反应的一种机制。然而,MCT通过内质网(ER)应力引起的肝细胞凋亡的潜在机制仍然不完全理解。在这项研究中,我们描述了ER应激在大鼠中诱导肝毒性的作用。将24只雄性大鼠随机分为3组:生理盐水组,45mg / kg MCT组和90mg / kg MCT组。经过48小时的盐水/ MCT给药后,通过蛋白质印迹进行肝脏分析ER应激相关蛋白质。 GRP78,P-IRE1α,ATF6和Caspase-12的表达显示出剂量依赖性增加。 Perk / EIF2α/ ATF4 / Chop路径是细胞存活所需的主要ER应激途径之一。因此,通过分析MCT对该途径的影响,我们发现P-PERK,P-EIF2α,ATF4和Chec的蛋白质水平明显增加。所有这些结果表明MCT在大鼠肝脏中诱导ER应激。 Perk / EIF2α/ ATF4 / Chop途径参与了大鼠肝脏中MCT诱导的ER应激的调节。

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