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肠道微生物群参与毒死蜱诱导的小鼠亚慢性毒性作用。

Involvement of gut microbiota in chlorpyrifos-induced subchronic toxicity in mice.

作者信息

Song Xiaohua, Li Xinyi, Wang Yuzhen, Wu Yi-Jun

机构信息

Laboratory of Molecular Toxicology, State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, 1-5 Beichenxilu Road, Beijing, 100101, China.

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

出版信息

Arch Toxicol. 2025 Mar;99(3):1237-1252. doi: 10.1007/s00204-024-03934-9. Epub 2024 Dec 23.

Abstract

Chlorpyrifos (CPF) is one of the most widely used organophosphorus pesticides all over the world. Unfortunately, long-term exposure to CPF may cause considerable toxicity to organisms. Some evidence suggests that the intestinal microbial community may be involved in regulating the toxicity of CPF. In this study, we explored if the intestinal microbial community is involved in regulating the toxicity of CPF. Adult mice were continuously exposed to CPF (4 mg/kg body weight /day) for 10 weeks with or without a 2-week pretreatment of antibiotics to change the ecological structure of intestinal microorganisms in advance. Pathological changes in the liver and kidneys were examined and the biochemical parameters in serum for liver and kidney functions were detected, and changes in the intestinal microbial community of the mice were measured. The results showed that subchronic exposure to low-dose CPF caused an ecological imbalance in the intestinal flora and caused pathological damage to the liver and kidneys. Serum biochemical indicators for liver function such as alanine aminotransferase and total bile acids contents and renal biochemical indicators such as urea nitrogen and creatinine were disrupted. Changes in intestinal microbial community structure by using antibiotics in advance can effectively alleviate the pathological and functional damage to the liver and kidneys caused by CPF exposure. Further analysis showed that intestinal microorganisms such as Saccharibacteria (TM7), Odoribacter, Enterococcus and AF12 genera may be involved in managing the toxicity of CPF. Together, our results indicated that long-term low-dose CPF exposure could induce hepatotoxicity and nephrotoxicity, and liver and kidney damage may be mitigated by altering the ecology of intestinal microorganisms.

摘要

毒死蜱(CPF)是全球使用最广泛的有机磷农药之一。不幸的是,长期接触CPF可能会对生物体造成相当大的毒性。一些证据表明,肠道微生物群落可能参与调节CPF的毒性。在本研究中,我们探讨了肠道微生物群落是否参与调节CPF的毒性。成年小鼠连续10周暴露于CPF(4毫克/千克体重/天),同时进行或不进行为期2周的抗生素预处理,以提前改变肠道微生物的生态结构。检查肝脏和肾脏的病理变化,检测血清中肝功能和肾功能的生化参数,并测量小鼠肠道微生物群落的变化。结果表明,亚慢性低剂量CPF暴露导致肠道菌群生态失衡,并对肝脏和肾脏造成病理损伤。肝功能血清生化指标如谷丙转氨酶和总胆汁酸含量以及肾功能生化指标如尿素氮和肌酐均受到干扰。提前使用抗生素改变肠道微生物群落结构可有效减轻CPF暴露对肝脏和肾脏造成的病理和功能损伤。进一步分析表明,糖菌属(TM7)、气味杆菌属、肠球菌属和AF12属等肠道微生物可能参与CPF毒性的调控。总之,我们的结果表明,长期低剂量CPF暴露可诱导肝毒性和肾毒性,改变肠道微生物生态可减轻肝脏和肾脏损伤。

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