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Involvement of mitochondrial fission in renal tubular pyroptosis in mice exposed to high and environmental levels of glyphosate combined with hard water

机译:对小鼠肾小管糊死肌中的线粒体裂变的参与与硬水相结合的小和环境水平的小鼠

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Chronic interstitial nephritis in agricultural communities (CINAC) has reached epidemic proportions. The combination of glyphosate and hard water has been postulated to play a potent aetiological role in CINAC. Therefore, dynamin-related protein 1 (Drp1)-mediated aberrant mitochondrial fission and subsequent activation of the nucleotide-binding oligomerization domain (NOD)-like receptor protein 3 (Nlrp3)/caspase1 pathway may be involved in the pathogenesis of nephropathy. In the present study, mice were sub-chronically exposed to high doses and environmental levels of glyphosate (100 mg/kg body weight (mg/kg.bw) glyphosate in Roundup and 0.7 mg/L pure glyphosate, respectively) and hard water (2500 mg/L CaCO3 and 250 mg/L Ca2+, respectively) in drinking water. Moreover, Mdivi-1 (Md-1, 10 mg/kg.bw) was intraperitoneally injected to inhibit Drp1 on the basis of the high-dose experiment. Histopathological examination, biochemical analysis, ELISA, western blotting and fluorescent staining were used to analyse renal structure, renal tubular pyroptosis and mitochondrial fission/fusion alterations. The results showed dramatic proximal tubular injury, particularly in the combined groups. Moreover, significant increases in the protein expression levels of calmodulin (CaM), calmodulin-dependent protein kinase II (CaMKII), Drp1/p-Drp1-Ser616 and the Txnip/Nlrp3/caspase1 signalling pathway, and alterations in oxidative stress were observed in the combined groups, and these effects were attenuated by the Drp1 inhibitor Md-1. Intriguingly, there may be a synergistic effect of glyphosate and hard water on renal injury. Taken together, these results suggest that the combination of glyphosate and hard water, even at environmental exposure levels, enhances pyroptosis and ongoing tubulointerstitial inflammation through excessive Drp1-mediated mitochondrial fission. (C) 2021 Elsevier Ltd. All rights reserved.
机译:农业社区慢性间质性肾炎(CINAC)已达到流行病的比例。草甘膦和硬水的组合已经假设在Cinac中起着巨大的安全性作用。因此,发动蛋白相关的蛋白质1(DRP1)介导的异常线粒体裂变和随后的核苷酸结合寡聚化结构域(NOOD) - 样受体蛋白3(NORP3)/ caspase1途径的激活可以参与肾病的发病机制。在本研究中,小鼠将亚常长的小剂量和环境水平的草甘膦(100mg / kg体重(mg / kg.bw)草甘膦分别为圆形和0.7mg / L纯草甘膦)和硬水( 2500毫克/升CACO3和250 mg / L CA2 +,分别)在饮用水中。此外,MDivi-1(MD-1,10mg / kg.bw)在高剂量实验的基础上腹膜内注射以抑制DRP1。组织病理学检查,生物化学分析,ELISA,蛋白质印迹和荧光染色用于分析肾结构,肾小管糊化瘤和线粒体裂变/融合改变。结果表明初步近端管状损伤,特别是在合并组中。此外,观察到钙调蛋白(CAM),钙调蛋白依赖性蛋白激酶II(CAMKII),DRP1 / P-DRP1-SER616和TXNIP / NLRP3 / CASPASE1信号传导途径的显着增加,并观察到氧化应激的改变组合基团和这些效果由DRP1抑制剂MD-1衰减。有趣的是,对草甘膦和硬水对肾损伤的硬水可能有协同作用。总之,这些结果表明草甘膦和硬水的组合,即使在环境暴露水平,通过过量的DRP1介导的线粒体裂变增强了γ凋亡和持续的细胞间隔炎。 (c)2021 elestvier有限公司保留所有权利。

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