Battery wastewater induces nephrotoxicity via disordering the mitochondrial dynamics

电池(电) 废水 自噬 ATG5型 第一季 MFN2型 生物 细胞凋亡 环境科学 环境工程 生物化学 线粒体融合 基因 线粒体DNA 功率(物理) 物理 量子力学
作者
Jiangnan Yi,Jianzhao Liao,Bin Tian,Bole Wang,Yangzom Chamba,Zulfiqar Ahmed,Khalid Mehmood,Rao Zahid Abbas,Ying Liu,Zhaoxin Tang,Hui Zhang
出处
期刊:Chemosphere [Elsevier]
卷期号:303: 135018-135018 被引量:10
标识
DOI:10.1016/j.chemosphere.2022.135018
摘要

The rapid development of new energy battery enterprises manifolds the obsolete and scrapped batteries which are considered serious concern for the environment and ecology. Increasing trend of recycling batteries waste is public hazard throughout the world. The batteries wastes affect the various body systems but exact toxicological mechanism of battery wastewater is still unexplored. The present study was designed to observe the toxicological effects of batteries wastes on kidney functional dynamics. In this experiment, a total of 20 male mice were randomly divided into two groups including control and treatment (battery wastewater) group. The control group was provided the normal saline while the battery wastewater group were provided battery waste-water for a period of 21 days. The isolated kidneys were processed for histopathological analysis, biochemical assays, mRNA and protein estimation. The results showed that battery wastewater provision increased the mitochondrial division-related genes and proteins (Drp1, MFF, Fis1) and decreased the expression level of fusion-related nuclear proteins (MFN1, MFN2, OPA1) in kidneys. Moreover, the battery wastewater exposure significantly up-regulated the autophagy (PINK, Parkin, mTOR, ATG5, LC3-b, p62) and apoptosis (Bax, Cytc, APAF1, P53, Caspase3, Caspase8) related mRNA and proteins levels in kidneys. However, down-regulation of mRNA and proteins levels of Bcl2 and Beclin1 were also observed in kidneys after batteries wastes exposure. In conclusion, it is evident that the battery wastewater leads to renal apoptosis and autophagy by disrupting the mitochondrial dynamics in mice kidneys.
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