Role of kinins in the endothelial protective effect of ischaemic preconditioning
- 3 February 1998
- journal article
- Published by Wiley in British Journal of Pharmacology
- Vol. 123 (3), 413-420
- https://doi.org/10.1038/sj.bjp.0701619
Abstract
1. The aim of this study was to assess whether the protective effect of ischaemic preconditioning on endothelial function in coronary arteries of the rat involves kinins. 2. Isolated hearts of the rat were exposed to a 30-min low-flow ischaemia (flow rate of 1 ml min[-1]) followed by 20-min reperfusion, after which coronaries were precontracted with 0.1 microM U-46619, and the response to the endothelium-dependent vasodilator, 5-hydroxytryptamine (5-HT, 10 microM), compared to that of the endothelium-independent vasodilator, sodium nitroprusside (SNP, 3 microM). 3. In untreated hearts, ischaemia-reperfusion diminished selectively 5-HT-induced vasodilatation, compared with time-matched sham hearts. The vasodilatation to SNP was unaffected after ischaemia-reperfusion. Preconditioning (5 min of zero-flow ischaemia followed by 10 min reperfusion) in untreated hearts preserved the vasodilatation produced by 5-HT. 4. Blockade of B1 and B2 receptors with either 3 nM [Lys[0], Leu8, des-Arg9]-bradykinin (LLDBK) or 10 nM Hoe 140 (icatibant), respectively, (started 15 min before ischaemic preconditioning or a corresponding sham period and stopped just before the 20-min reperfusion period) had no effect on the vasodilatation produced by either 5-HT or SNP in sham hearts. Pretreatment with Hoe 140 did not block the protective effect of ischaemic preconditioning on the 5-HT vasodilatation. In contrast, LLDBK halved the protective effect of ischaemic preconditioning on endothelium-dependent vasodilatation. 5. Perfusion with either bradykinin or des-Arg9-bradykinin (1 nM) 30 min before and lasting throughout the ischaemia protected the endothelium. 6. In conclusion, ischaemic preconditioning affords protection to the endothelial function in coronary resistance arteries of the rat partly by activation of B1 receptors. Although exogenous BK perfusion can protect the endothelium, B2 receptors do not play an important role in this protection in the rat isolated heart.Keywords
This publication has 30 references indexed in Scilit:
- Structure-Activity Studies of B 1 Receptor–Related PeptidesHypertension, 1996
- Bradykinin as an endogenous myocardial protective substance with particular reference to ischemic preconditioning–a brief review of the evidenceCanadian Journal of Physiology and Pharmacology, 1995
- Evidence that prostaglandins I2, E2, and D2 may activate ATP sensitive potassium channels in the isolated rat heartCardiovascular Research, 1994
- Protective effects of ATP sensitive potassium channel openers in models of myocardial ischaemiaCardiovascular Research, 1994
- KATP channels in ischaemic preconditioningCardiovascular Research, 1994
- Nonendothelial‐derived nitric oxide activates the ATP‐sensitive K+ channel of vascular smooth muscle cellsFEBS Letters, 1994
- Infarct size limitation by preconditioning: its phenomenological features and the key role of adenosineCardiovascular Research, 1993
- 5-Hydroxytryptamine mediates endothelium dependent coronary vasodilatation in the isolated rat heart by the release of nitric oxideCardiovascular Research, 1991
- Local Inhibition of Bradykinin Degradation in Ischemic HeartsJournal of Cardiovascular Pharmacology, 1990
- Reperfusion after acute coronary occlusion in dogs impairs endothelium-dependent relaxation to acetylcholine and augments contractile reactivity in vitro.Journal of Clinical Investigation, 1987