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POP 诱导肥胖的机制新见解:来自 DDE 改变的微生物组的证据。

New insight into the mechanism of POP-induced obesity: Evidence from DDE-altered microbiota.

机构信息

Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Science, China Agricultural University, No. 2, West Yuanmingyuan Road, Beijing, 100193, PR China; College of Chemistry and Biological Engineering, University of Science and Technology Beijing, No. 30, Xueyuan Road, Beijing, 100083, PR China.

Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Science, China Agricultural University, No. 2, West Yuanmingyuan Road, Beijing, 100193, PR China.

出版信息

Chemosphere. 2020 Apr;244:125123. doi: 10.1016/j.chemosphere.2019.125123. Epub 2019 Oct 16.

Abstract

Although epidemiological studies demonstrate that persistent organic pollutants (POPs) could lead to metabolic syndrome, the mechanism has remained unclear. The dysbiosis of gut microbiota and the lipid metabolome have been put forward in the pathophysiology of metabolic syndrome. In this study, we used dichlorodiphenyldichloroethylene (DDE) as an example to study the effects of POP-impaired microbial composition and metabolome homeostasis on metabolic syndrome. The results showed that DDE exposure increased body weight and fat content and impaired glucose homeostasis. Further investigation revealed that DDE induced gut dysbiosis as indicated by an increased Firmicutes-to-Bacteroidetes ratio, which may impact energy harvest efficiency. Meanwhile, the plasma lipid metabolome profile was significantly altered by DDE. Furthermore, phosphatidylcholine, phosphatidylserine, phosphatidylethanolamine, and triacylglycerol were identified as key metabolites affected by DDE treatment, and these altered lipid metabolites were highly correlated with changed microbiota composition. This study provides novel insight into the underlying mechanism of POP-induced obesity and diabetes, pointing to gut microbiota as one of the targets.

摘要

尽管流行病学研究表明持久性有机污染物(POPs)可能导致代谢综合征,但具体机制尚不清楚。肠道微生物组和脂质代谢组的失调已被提出作为代谢综合征的病理生理学机制。在这项研究中,我们以二氯二苯二氯乙烯(DDE)为例,研究了 POP 破坏的微生物组成和代谢组稳态对代谢综合征的影响。结果表明,DDE 暴露会增加体重和脂肪含量,并损害葡萄糖稳态。进一步的研究表明,DDE 诱导的肠道微生物组失调表现为厚壁菌门与拟杆菌门比值增加,这可能影响能量收获效率。同时,DDE 显著改变了血浆脂质代谢组谱。此外,鉴定出 DDE 处理后受影响的关键代谢物有磷脂酰胆碱、磷脂酰丝氨酸、磷脂酰乙醇胺和三酰基甘油,这些改变的脂质代谢物与改变的微生物组成高度相关。本研究为 POP 诱导肥胖和糖尿病的潜在机制提供了新的见解,提示肠道微生物组是其中的一个靶点。

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