卵巢切除术引起的动脉硬化与血管衰老不同,并通过GPER激活逆转
Isabella M Kilanowski-Doroh1, Alexandra B McNally1, Tristen J Wong1
1Department of Pharmacology, Tulane School of Medicine, New Orleans, LA (I.M.K.-D., A.B.M., T.J.W., B.V., S.A.B., A.I.S., C.R., Z.D., A.C.H., S.H.L.).
Hypertension (Dallas, Tex. : 1979)
|March 6, 2024
概括
更年期和衰老通过不同的机制增加了小鼠的动脉硬. 雌激素受体激活,特别是LNS8801,可以逆转这种性,为女性提供潜在的治疗途径.
科学领域:
- 心血管生理学心血管生理学
- 内分泌学 在内分泌学.
- 血管生物学 血管生物学
背景情况:
- 动脉硬度是一个重要的心血管风险因素,在女性更年期过渡期间升级.
- 绝经后雌激素缺乏与动脉硬度增加有关.
研究的目的:
- 为了调查更年期的小鼠模型是否会复制衰老引起的动脉硬.
- 为了确定激活G蛋白结合雌激素受体是否可以逆转动脉硬性.
主要方法:
- 在雌性C57Bl/6J小鼠中诱导了卵巢切除 (手术更年期) 和衰老.
- 小鼠接受了与G蛋白结合的雌激素受体激动剂 (LNS8801和G-1).
- 评估了动脉刚性,血管几何形状和基因表达 (RNA测序).
主要成果:
- 卵巢切除和衰老都会同样增加脉冲波速度,独立于血压.
- 衰老导致动脉壁变厚,而卵巢切除增加了材料的刚性,而没有几何变化.
- 卵巢切除降低了光滑肌肉收缩基因的调节;LNS8801有效地逆转了卵巢切除小鼠的性.
结论:
- 卵巢切除和衰老通过不同的途径诱导动脉硬化.
- 雌激素的损失会影响血管健康,影响物质特性和光滑肌肉功能.
- LNS8801在逆转更年期动脉硬性方面表现有前途,这表明它有可能在女性中临床应用.
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