Modulatory effect of bradykinin on the release of noradrenaline from rat isolated atria
Autor: | Réjean Couture, Sylvain Foucart, Chantal Chulak |
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Jazyk: | angličtina |
Rok vydání: | 1995 |
Předmět: |
Agonist
Male medicine.medical_specialty Bisindolylmaleimide Diclofenac Indoles medicine.drug_class Adrenergic beta-Antagonists Bradykinin Maleimides chemistry.chemical_compound Norepinephrine Internal medicine medicine Animals Drug Interactions Heart Atria Rats Wistar Protein kinase C Phorbol 12 13-Dibutyrate Protein Kinase C Fenoterol Pharmacology Analysis of Variance Dose-Response Relationship Drug Angiotensin II Kinin Receptor antagonist Electric Stimulation Rats Endocrinology chemistry Second messenger system Research Article |
Popis: | 1. We investigated the modulation by bradykinin (BK) of electrically induced noradrenaline release in rat isolated atria preincubated with [3H]-noradrenaline. 2. BK (1-100 nM) enhanced significantly the stimulation-induced outflow of radioactivity in a concentration-dependent manner with a calculated EC50 of 0.58 nM. 3. Des-Arg9-BK (0.1-100 nM), a selective B1 receptor agonist, did not modify the stimulation-induced outflow of radioactivity. Hoe 140 (10 nM), a selective B2 receptor antagonist, but not [Leu8]-des-Arg9-BK (100 nM), a selective B1 receptor antagonist, blocked the facilitatory effect of BK. 4. The effect of BK was not affected by diclofenac (1 microM), a cyclo-oxygenase inhibitor. Bisindolylmaleimide (1 microM), a protein kinase C inhibitor, significantly reduced the facilitatory effect of BK (10 nM), angiotensin II (0.3 microM) and phorbol dibutyrate (0.1 and 1 microM) but not of fenoterol (1 microM). 5. The results suggest that BK enhances noradrenaline release via a prejunctional B2 kinin receptor in the rat atrium. The effect appears to involve protein kinase C as a second messenger. |
Databáze: | OpenAIRE |
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