从病理生理学上相关的双S暴露通过破坏棕色脂肪组织调节的能量代谢来加速衰老
1Department of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu 610041, China.
概括
双S (BPS) 是一种常见的BPA替代品,在相关暴露水平下加速和老鼠的衰老. 这种衰老效应与棕色脂肪组织 (BAT) 中的BPS积累和功能障碍有关.
科学领域:
- 环境健康 环境健康
- 衰老研究研究 衰老研究
- 毒理学 毒理学 毒理学
背景情况:
- 双A (BPA) 替代品在消费品和与食品接触的材料中普遍存在.
- 从病理生理学上相关的BPA替代品度对衰老的影响尚不清楚.
- 双S (BPS) 是一个广泛使用的BPA替代品.
研究的目的:
- 为了研究五种BPA替代品对衰老的影响,使用*Caenorhabditis elegans* (*C. elegans*) 和小鼠模型.
- 检查BPA替代品诱导衰老的潜在机制,重点关注双S (BPS).
主要方法:
- 暴露C. elegans和小鼠在五种BPA替代品的病理生理学相关度下.
- 对暴露生物体的衰老表型,寿命和健康寿命的评估.
- 分析小鼠组织中BPS积累的情况,特别是棕色脂肪组织 (BAT).
- 最佳技术的RNA测序,以确定受BPS影响的衰老途径.
- 在小鼠中进行了BAT移植实验,以评估BAT在BPS诱导的衰老中的作用.
主要成果:
- 暴露于相关度的双S (BPS) 加快了C. elegans*的衰老.
- 在小鼠中,BPS暴露减少了寿命和健康期,并加速了多种组织中的衰老表型.
- BPS在棕色脂肪组织 (BAT) 中大量积累,并通过多种途径加速其衰老.
- BAT移植证实了其作用:BPS暴露的BAT加速了接受者的衰老,而未暴露的BAT改善了暴露的小鼠的代谢状态和延迟衰老.
结论:
- 从病理生理学上相关的双S (BPS) 度在C. elegans和小鼠中加速衰老.
- BPS的衰老效应显著通过色脂肪组织 (BAT) 功能中断的中介.
- 这些发现凸显了与BPS暴露相关的潜在健康风险,特别是与衰老有关.
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