| Literature DB >> 25732873 |
Ting Wang1, Xuehui Li2, Dongxu Yang3, Hongtao Zhang2, Peng Zhao2, Juanling Fu3, Biyun Yao4, Zongcan Zhou5.
Abstract
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-6α, 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.Entities:
Keywords: Apoptosis; Endoplasmic reticulum stress; Manganese; Neurotoxicity; Striatum
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Year: 2015 PMID: 25732873 DOI: 10.1016/j.neuro.2015.02.007
Source DB: PubMed Journal: Neurotoxicology ISSN: 0161-813X Impact factor: 4.294