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低剂量氯虫苯甲酰胺和甲氨基阿维菌素苯甲酸盐亚慢性暴露对大鼠肾脏代谢的影响

Subchronic Exposure to Low-Dose Chlorfenapyr and Emamectin Benzoate Disrupts Kidney Metabolism in Rats.

作者信息

Zhang Di, Song Xiao-Hua, Yang Dan, Ge Mu-Zi, Qiu Jun, Jiang Han-Qing, Sun Yan-Yan, Li Xiang-Dong, Wu Yi-Jun

机构信息

State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Toxics. 2025 Jan 20;13(1):65. doi: 10.3390/toxics13010065.

Abstract

Residues of the pesticides chlorfenapyr (CFP) and emamectin benzoate (EMB) often coexist in the environment and can be accumulated in the body. To understand the impact of these two chemicals on health, we investigated their effect on the kidneys. In this study, rats were treated with CFP and/or EMB at low/medium/high doses of 1/3/9 mg/kg/day and 0.2/0.6/1.8 mg/kg/day, respectively, via oral gavage for 60 days. Kidneys and serum samples were collected and serum biochemistry and kidney histopathological changes were analyzed and examined. Kidney metabolome alterations were analyzed by using gas chromatography-mass spectrometry. The results showed that combined exposure to CFP and EMB elevated BUN levels and induced pathological damage, which presented as thinner renal tubular epithelial cells, an abnormal glomerular morphology, and an increased fibrotic area. CFP and/or EMB disrupted glutathione metabolism and carbohydrate metabolism, resulting in the alteration of kidney metabolomes and inducing oxidative stress in the cells of kidney tissues. In addition, CFP decreased ATP content and inhibited pyruvate PDH activity in the kidneys. These findings suggest that long-term exposure to CFP and EMB at environmentally relevant levels induce alterations in the renal metabolome, oxidative stress, and an insufficient energy supply, which may contribute to renal histopathological damage.

摘要

杀虫剂溴虫腈(CFP)和甲氨基阿维菌素苯甲酸盐(EMB)的残留物经常共存于环境中,并可在体内蓄积。为了解这两种化学物质对健康的影响,我们研究了它们对肾脏的作用。在本研究中,大鼠分别通过灌胃给予低/中/高剂量(1/3/9毫克/千克/天和0.2/0.6/1.8毫克/千克/天)的CFP和/或EMB,持续60天。收集肾脏和血清样本,并分析和检查血清生化指标以及肾脏组织病理学变化。采用气相色谱-质谱联用技术分析肾脏代谢组的改变。结果表明,联合暴露于CFP和EMB会升高尿素氮水平并引发病理损伤,表现为肾小管上皮细胞变薄、肾小球形态异常以及纤维化面积增加。CFP和/或EMB扰乱了谷胱甘肽代谢和碳水化合物代谢,导致肾脏代谢组发生改变,并在肾脏组织细胞中诱导氧化应激。此外,CFP降低了肾脏中的三磷酸腺苷(ATP)含量并抑制了丙酮酸脱氢酶(PDH)的活性。这些发现表明,在与环境相关的水平下长期暴露于CFP和EMB会导致肾脏代谢组改变、氧化应激以及能量供应不足,这可能会导致肾脏组织病理学损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3540/11769156/c5939db9e462/toxics-13-00065-g001.jpg

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