The effect of bradykinin and its antagonist on survival time after coronary artery occlusion in hypertensive rats

被引:12
作者
Abbas, SA [1 ]
Sharma, JN [1 ]
Yusof, APM [1 ]
机构
[1] Univ Sains Malaysia, Sch Pharmaceut Sci, Dept Physiol & Pharmacol, Penang 11800, Malaysia
来源
IMMUNOPHARMACOLOGY | 1999年 / 44卷 / 1-2期
关键词
coronary artery occlusion; blood pressure; arrhythmias; cardiac kinins;
D O I
10.1016/S0162-3109(99)00155-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It is known that BK does play a role in the cardioprotective effect of angiotensin converting enzyme (ACE) inhibitors. The present study therefore was conducted to examine the effects of bradykinin (BK) and its antagonist on survival time in spontaneously hypertensive rats (SHR) with coronary artery ligation for 15 min and continuously. We also evaluated the heart rate and blood pressure (BP) in the presence and absence of BK and BK2 receptor antagonist, D-Arg-[Hyp-D-Phe(7)]BK. Coronary artery was Ligated in anaesthetized rats and they were artificially ventilated with room air (stroke volume, 4 ml; 48 strokes/min) as described by the previous investigators. Lead II elecrocardiogram (ECG) was recorded from subcutaneous steel needle electrodes. Results of this investigation indicated that BK treatment 4 mu g/kg (i.v.) and 8 mu g/kg (i.v.) caused significant (P < 0.05) increase in survival time in SHR with coronary artery ligation for 15 min and continuously as compare to their respective saline-treated controls. However, BK antagonist treatment 4 mu g/kg (i.v.) abolished the increase in survival time caused by BK treatment. The mean values of survival time between the saline-treated and BK antagonist plus BK-treated rats did not differ significantly (P > 0.05). The heart rate and BP responses were greatly reduced (P < 0.001) in the presence of coronary artery ligation. These findings suggest that BK might have cardioprotective effect to increase the survival time in rats by activating BK, receptors after coronary artery ligation. (C) 1999 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:93 / 98
页数:6
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