发育低剂量双A暴露导致了广泛的转录组女性男性化和男性女性化在以后的生活中
Thomas Lind1, Linda Dunder2, Margareta H Lejonklou2
1Department of Medical Sciences, Section of Clinical Pharmacogenomics and Osteoporosis, Uppsala University, Uppsala, Sweden. thomas.lind@medsci.uu.se.
Communications medicine
|October 1, 2025
概括
在小鼠中,低剂量双A (BPA) 的发育暴露显著改变了骨髓基因表达和血液代谢. 这种内分泌干扰剂通过影响T细胞可能会诱导男性的代谢综合征.
科学领域:
- 内分泌学 在内分泌学.
- 毒理学 毒理学 毒理学
- 代谢学 代谢学 代谢学
背景情况:
- 双甲 (BPA) 是一种与代谢疾病相关的内分泌干扰物.
- 在子宫内BPA暴露可能特别影响骨髓 (BM).
研究的目的:
- 研究低剂量BPA对大鼠BM转录组和血液代谢概况的影响.
- 将BPA诱导的变化与人类代谢综合征 (MetS) 相比较.
主要方法:
- 菲舍尔344大鼠对低剂量BPA的发育暴露.
- 分析BM转录组和血液代谢概况.
- 与人类MetS队列进行比较.
主要成果:
- 在低剂量BPA时观察到的性别特异的BM转录组变化.
- BPA诱导的低代谢 (女性) 和高代谢 (男性) 状态.
- 血液代谢概况与人类的MetS有明显的重叠.
结论:
- 低剂量BPA暴露可能通过T细胞效应诱导男性特异性代谢综合征.
- 提供了支持BPA.低可容忍每日摄入量 (TDI) 的证据.
- 突出了内分泌干扰物的性别特异性影响.
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