ангиотензин II 1 型受体阻塞可以预防酒精性心肌病
Che-Ping Cheng1, Heng-Jie Cheng, Carol Cunningham
1Cardiology Section, Department of Internal Medicine, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1045, USA. ccheng@wfubmc.edu
Circulation
|July 13, 2006
概括
饮酒会激活氨酸 - 血管素系统 (RAS),导致酒精性心肌病. 用伊尔贝沙坦阻断血管激素II (Ang II) 类型1受体 (AT1) 可以防止这种心脏功能障碍.
科学领域:
- 心脏病学 心脏病学
- 药理学 药理学是指药理学的学科.
- 毒理学 毒理学 毒理学
背景情况:
- 酒精性心肌病是一种慢性饮酒的潜在后果.
- 氨酸-血管素系统 (RAS) 可能在酒精性心肌病的发展中发挥作用.
研究的目的:
- 为了研究血管素II (Ang II) 类型1受体 (AT1) 阻断对酒精性心肌病发展的影响.
- 评估伊尔贝萨坦对饮酒狗的心脏功能和RAS激活的影响.
主要方法:
- 带有仪器的狗被分为三个组:酒精,酒精加伊尔贝沙坦和对照组.
- 左心室 (LV) 和心肌细胞功能,以及RAS标志物,在6个月内进行了监测.
- 测量包括 LV 收缩性,肌细胞缩短和重新延长以及过渡性.
主要成果:
- 摄入酒精导致持续的RAS激活,由增加的Ang II,蛋白活性和AT1受体表达体现出来.
- 心脏功能障碍表现为LV收缩性降低,肌细胞功能受损和减少处理.
- 伊尔贝沙坦治疗预防了酒精诱导的心脏功能障碍,并抑制了RAS激活.
结论:
- 慢性饮酒会激活RAS,导致心脏功能障碍逐渐恶化.
- 阻断AT1受体可以有效地预防酒精性心肌病的发展.
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