摘要
目的 :研究血管紧张素 (1 7) [Ang (1 7) ]对正常豚鼠心室肌细胞L 型钙离子通道的影响 ,旨在探讨Ang (1 7)发挥降压作用的离子通道及分子基础。 方法 :应用膜片钳全细胞记录技术。结果 :Ang (1 7)可使ICa L呈浓度依赖性增加 ,选择性AngⅠ型 (AT1)受体拮抗剂缬沙坦或非选择性AT1受体拮抗剂Sarthran(Sar)均可消除Ang (1 7)增加ICa L的作用。结论 :Ang (1 7)通过AT1受体增加ICa L,其降压作用不是通过抑制钙离子内流而实现的。
Objective:To investigate the mechanism of hypotensive effects of angiotensin(Ang)-(1-7) in guinea pig.Methods:Membrane currents were recorded with patch electrodes in a whole-cell clamp configuration.Results:The present results showed that: I Ca-L was increased by Ang-(1-7) in a concentration dependent manner. The effects of Ang-(1-7) on I Ca-L can be eliminated by specific AT 1 antagonist Valsartan and non-specific AT antagonist Sarthran.Conclusion:These results suggest that: Ang-(1-7) increase the amplitude of I Ca-L through AT 1 receptor. The hypotensive effects of Ang-(1-7) have no relationship with inward calcium current increase.
出处
《临床心血管病杂志》
CAS
CSCD
北大核心
2003年第11期674-676,共3页
Journal of Clinical Cardiology
关键词
血管紧张素
心肌
钙离子通道
电生理学
Angiotensin
Myocardium
Calcium channels
Electrophysiology