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母体暴露于低剂量 BDE-47 会导致后代体重增加和胰岛素敏感性受损。

Maternal Exposure to Low-Dose BDE-47 Induced Weight Gain and Impaired Insulin Sensitivity in the Offspring.

机构信息

Helmholtz Centre for Environmental Research-UFZ, Department of Environmental Immunology, 04318 Leipzig, Germany.

Department of Dermatology, Venerology and Allergology, Leipzig University Medical Center, University of Leipzig, 04318 Leipzig, Germany.

出版信息

Int J Mol Sci. 2024 Aug 7;25(16):8620. doi: 10.3390/ijms25168620.

Abstract

Polybrominated diphenyl ethers (PBDEs), commonly used as synthetic flame retardants, are present in a variety of consumer products, including electronics, polyurethane foams, textiles, and building materials. Initial evidence from epidemiological and experimental studies suggests that maternal PBDE exposure may be associated with a higher BMI in children, with disturbance of energy metabolism and an increased risk of Type 2 diabetes. However, the causality between early exposure to real-life PBDE concentrations and increased weight as well as mechanisms underlying impaired metabolic pathways in the offspring remain elusive. Here, using a mouse model we examined the effect of maternal exposure to 2,2',4,4'-tetrabrominated diphenyl ether (BDE-47), the most abundant congener in human samples, on offspring weight gain and energy homeostasis using a mouse model. Maternal exposure to BDE-47 at low dose resulted in weight gain in female offspring together with an impaired glucose and insulin tolerance in both female and male mice. In vitro and in vivo data suggest increased adipogenesis induced by BDE-47, possibly mediated by DNA hypermethylation. Furthermore, mRNA data suggest that neuronal dysregulation of energy homeostasis, driven via a disturbed leptin signaling may contribute to the observed weight gain as well as impaired insulin and glucose tolerance.

摘要

多溴联苯醚(PBDEs)作为常用的合成型阻燃剂,存在于多种消费品中,包括电子产品、聚氨酯泡沫、纺织品和建筑材料。流行病学和实验研究的初步证据表明,母体 PBDE 暴露可能与儿童 BMI 升高、能量代谢紊乱和 2 型糖尿病风险增加有关。然而,早期接触实际 PBDE 浓度与体重增加之间的因果关系,以及后代代谢途径受损的机制仍不清楚。在这里,我们使用一种小鼠模型,研究了母体暴露于 2,2',4,4'-四溴联苯醚(BDE-47)对后代体重增加和能量平衡的影响,BDE-47 是人类样本中最丰富的同系物。母体低剂量暴露于 BDE-47 会导致雌性后代体重增加,同时雌性和雄性小鼠的葡萄糖和胰岛素耐量受损。体外和体内数据表明,BDE-47 可能通过 DNA 超甲基化引起脂肪生成增加。此外,mRNA 数据表明,能量平衡的神经元失调,通过扰乱瘦素信号传递,可能导致观察到的体重增加以及胰岛素和葡萄糖耐量受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b98e/11354368/ef978a7fba3e/ijms-25-08620-g006.jpg

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