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

Citation
Sa. Abbas et al., The effect of bradykinin and its antagonist on survival time after coronary artery occlusion in hypertensive rats, IMMUNOPHARM, 44(1-2), 1999, pp. 93-98
Citations number
20
Categorie Soggetti
Immunology
Journal title
IMMUNOPHARMACOLOGY
ISSN journal
01623109 → ACNP
Volume
44
Issue
1-2
Year of publication
1999
Pages
93 - 98
Database
ISI
SICI code
0162-3109(19991015)44:1-2<93:TEOBAI>2.0.ZU;2-0
Abstract
It is known that BK does play a role in the cardioprotective effect of angi otensin 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 ant agonist, D-Arg-[Hyp-D-Phe(7)]BK. Coronary artery was Ligated in anaesthetiz ed 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 electrod es. 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 c ompare to their respective saline-treated controls. However, BK antagonist treatment 4 mu g/kg (i.v.) abolished the increase in survival time caused b y 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 t he presence of coronary artery ligation. These findings suggest that BK mig ht have cardioprotective effect to increase the survival time in rats by ac tivating BK, receptors after coronary artery ligation. (C) 1999 Published b y Elsevier Science B.V. All rights reserved.