College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, China; Institute of Poisonous Plants in Western China, Northwest A&F University, Yangling, Shaanxi 712100, China.
Department of Biotechnology, Guizhou Medical University, Guiyang, Guizhou 550004, China.
Res Vet Sci. 2020 Jun;130:237-239. doi: 10.1016/j.rvsc.2020.03.021. Epub 2020 Mar 14.
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 hepatotoxicity 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-IRE1α, ATF6 and caspase-12 showed a dose-dependent increase. PERK/eIF2α/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-eIF2α, ATF4 and CHOP were increase obviously. All these results indicate that MCT induces ER stress in rat liver. The PERK/eIF2α/ATF4/CHOP pathway is involved in the regulation of MCT-induced ER stress in the liver of rat.
野百合碱(MCT)属于吡咯里西啶生物碱(PAs),是 Crotalaria Lin 中重要的肝毒性生物碱之一。细胞凋亡是 MCT 诱导的毒性反应的一种机制。然而,MCT 通过内质网(ER)应激引起肝凋亡的潜在机制仍不完全清楚。在这项研究中,我们描述了 ER 应激在 MCT 诱导大鼠肝毒性中的作用。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。在给予生理盐水/MCT 48 小时后,收集肝脏,通过 Western blot 分析 ER 应激相关蛋白。GRP78、p-IRE1α、ATF6 和 caspase-12 的表达呈剂量依赖性增加。PERK/eIF2α/ATF4/CHOP 途径是 ER 应激的主要途径之一,对细胞存活至关重要。因此,通过分析 MCT 对该途径的影响,我们发现 p-PERK、p-eIF2α、ATF4 和 CHOP 的蛋白水平明显增加。所有这些结果表明 MCT 诱导大鼠肝内质网应激。PERK/eIF2α/ATF4/CHOP 途径参与调节 MCT 诱导的大鼠肝内质网应激。