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草甘膦与硬水联合诱导的肾小管损伤:胞质型磷脂酶A2的作用

Renal tubular injury induced by glyphosate combined with hard water: the role of cytosolic phospholipase A2.

作者信息

Wang Ruojing, Chen Jing, Ding Fan, Zhang Lin, Wu Xuan, Wan Yi, Hu Jianying, Zhang Xiaoyan, Wu Qing

机构信息

School of Public Health and Key Laboratory of Public Health Safety of the Ministry of Education, Fudan University, Shanghai, China.

Department of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Ann Transl Med. 2021 Jan;9(2):130. doi: 10.21037/atm-20-7739.

Abstract

BACKGROUND

The combined effects of glyphosate and hard water on chronic kidney disease of unknown etiology (CDKu) have attracted much interest, but the mechanisms remain unknown. Cytoplasmic phospholipase A (cPLA) plays a key role in the acute and chronic inflammatory reactions. This study explored the effect of glyphosate combined with hard water on renal tubules and the possible targets and mechanisms involved.

METHODS

experiments were conducted to investigate the synergistic effects and potential mechanisms of glyphosate and hard water on renal tubular injury in mice.

RESULTS

Administration of glyphosate in mice resulted in elevated levels of β2-microglobulin (β-MG), albumin (ALB), and serum creatinine (SCr) compared to control mice. This increase was more pronounce when glyphosate was combined with hard water. In the glyphosate-treated mice, small areas of the kidney revealed fibroblast proliferation and vacuolar degeneration, particularly at the higher dose of 400 mg/kg glyphosate. However, the combination of glyphosate and hard water induced an even greater degree of pathological changes in the kidney. Immunofluorescence and western blot analyses showed that glyphosate and hard water had a coordinated effect on calcium ions (Ca)-activated phospholipase A and the activation may play a key role in inflammation and renal tubular injury. Exposure to glyphosate alone or glyphosate plus hard water increased the levels of oxidative stress markers and inflammatory biomarkers, namely, thromboxane A (TX-A), leukotriene B (LTB), prostaglandin E (PGE), nitric oxide synthase (NOS), and nitric oxide (NO). Parameters of oxidative stress, including the levels of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) were decreased. Further analysis showed that the levels of these biomarkers were significantly different between the mice treated with glyphosate plus hard water and the mice treated with glyphosate alone.

CONCLUSIONS

These findings suggested that hard water combined with glyphosate can induce renal tubular injury in mice, and this may involve mitogen-activated protein kinases (MAPK)/cytosolic phospholipase A (cPLA)/arachidonic acid (AA) and its downstream factors.

摘要

背景

草甘膦和硬水对病因不明的慢性肾脏病(CDKu)的联合影响引起了广泛关注,但其机制仍不清楚。细胞质磷脂酶A(cPLA)在急慢性炎症反应中起关键作用。本研究探讨了草甘膦与硬水联合作用对肾小管的影响以及可能涉及的靶点和机制。

方法

进行实验以研究草甘膦和硬水对小鼠肾小管损伤的协同作用及潜在机制。

结果

与对照小鼠相比,给小鼠施用草甘膦导致β2-微球蛋白(β-MG)、白蛋白(ALB)和血清肌酐(SCr)水平升高。当草甘膦与硬水联合使用时,这种升高更为明显。在草甘膦处理的小鼠中,肾脏的小区域出现成纤维细胞增殖和空泡变性,特别是在400mg/kg草甘膦的较高剂量下。然而,草甘膦和硬水的组合在肾脏中诱导了更严重的病理变化。免疫荧光和蛋白质印迹分析表明,草甘膦和硬水对钙离子(Ca)激活的磷脂酶A有协同作用,并且这种激活可能在炎症和肾小管损伤中起关键作用。单独暴露于草甘膦或草甘膦加硬水会增加氧化应激标志物和炎症生物标志物的水平,即血栓素A(TX-A)、白三烯B(LTB)、前列腺素E(PGE)、一氧化氮合酶(NOS)和一氧化氮(NO)。氧化应激参数,包括超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)的水平降低。进一步分析表明,草甘膦加硬水处理的小鼠与单独草甘膦处理的小鼠之间这些生物标志物的水平存在显著差异。

结论

这些发现表明,硬水与草甘膦联合可诱导小鼠肾小管损伤,这可能涉及丝裂原活化蛋白激酶(MAPK)/细胞质磷脂酶A(cPLA)/花生四烯酸(AA)及其下游因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a9/7867956/d1bce5408f1e/atm-09-02-130-f1.jpg

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