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首页> 外文期刊>Neurotoxicology >ER stress and ER stress-mediated apoptosis are involved in manganese-induced neurotoxicity in the rat striatum in vivo
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ER stress and ER stress-mediated apoptosis are involved in manganese-induced neurotoxicity in the rat striatum in vivo

机译:内质网应激和内质网应激介导的细胞凋亡在体内参与锰诱导的大鼠纹状体神经毒性

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摘要

Manganese (Mn) is an essential trace element found in many enzymes, however, excessive Mn-exposure can result in manganism which is similar to Parkinson's movement disorder. The mechanisms of manganism are not well-known. The present in vivo study was carried out to determine whether endoplasmic reticulum stress (ER stress) and ER stress-mediated apoptosis are involved in manganese-induced neurotoxicity. Sixty-four SD rats were randomly divided into four groups and were administered intraperitoneally with normal saline (NS, as control) or MnCl2 (7.5, 15 and 30 mg/kg body weight, respectively) for 4 weeks. We found that MnCl2 dose-dependently accumulate in striatal. HE staining and TUNEL assay results indicated that MnCl2 induced striatal neurocytes apoptosis in both male and female rats. The alterations of ultrastructures showed that MnCl2 resulted in chromatin condensation, mitochondria and ER tumefaction in rat striatal neurocytes. Furthermore, MnCl2 increased the expressions of p-IRE-1, ATF-6 alpha, PERK, GRP78, Sigma-1R, CHOP, Bim, Bax, caspase-12 and caspase-3, and decreased the expression of Bcl-2 in rat striatal neurocytes. In conclusion, MnCl2 could induce ER stress and ER stress-mediated apoptosis in rat striatal neurocytes, which might be one of the important mechanisms of Mn-induced neurotoxicity. (C) 2015 Elsevier Inc. All rights reserved.
机译:锰(Mn)是许多酶中必不可少的微量元素,但是,过量的Mn暴露会导致锰,这类似于帕金森氏症的运动障碍。锰的机制尚不为人所知。进行了本体内研究,以确定内质网应激(ER应激)和ER应激介导的细胞凋亡是否与锰诱导的神经毒性有关。将64只SD大鼠随机分为四组,分别腹腔注射生理盐水(NS,作为对照)或MnCl2(分别为7.5、15和30 mg / kg体重),持续4周。我们发现MnCl2剂量依赖性地积累在纹状体中。 HE染色和TUNEL分析结果表明,MnCl2诱导雄性和雌性大鼠纹状体神经细胞凋亡。超微结构的变化表明,MnCl2导致大鼠纹状体神经细胞中的染色质凝结,线粒体和ER肿瘤。此外,MnCl2增加大鼠中p-IRE-1,ATF-6 alpha,PERK,GRP78,Sigma-1R,CHOP,Bim,Bax,caspase-12和caspase-3的表达,并降低Bcl-2的表达。纹状体神经细胞。综上所述,MnCl2可以诱导大鼠纹状体神经细胞内质网应激和内质网应激介导的细胞凋亡,这可能是锰诱导的神经毒性的重要机制之一。 (C)2015 Elsevier Inc.保留所有权利。

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