Synergistic interaction of endogenous platelet-activating factor and vasopressin in generating angina in rats
| Autor: | Éva Morschl, János Nemcsik, Krisztina Kordás, F. A. László, József Egresits, Ferenc László, Imre Pavo |
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| Rok vydání: | 2004 |
| Předmět: |
Agonist
Male Vasopressin medicine.medical_specialty Receptors Vasopressin Time Factors Epinephrine medicine.drug_class Vasopressins Ornipressin Myocardial Ischemia Blood Pressure Angina Pectoris chemistry.chemical_compound Electrocardiography Lactones Phentolamine Hormone Antagonists Heart Rate Internal medicine medicine Animals Vasoconstrictor Agents Drug Interactions Platelet Activating Factor Rats Wistar Vasopressin receptor Pharmacology Dose-Response Relationship Drug business.industry Antagonist Receptor antagonist Rats Arginine Vasopressin Endocrinology Blood pressure Ginkgolides chemistry Injections Intravenous Diterpenes business Antidiuretic Hormone Receptor Antagonists medicine.drug |
| Zdroj: | European journal of pharmacology. 498(1-3) |
| ISSN: | 0014-2999 |
| Popis: | We examined the involvement of endogenous vasopressin and platelet-activating factor (PAF) in the pathogenesis of two types of experimental angina in urethane-anaesthetised male Wistar rats. In the first model, epinephrine (10 microg kg(-1)) was injected into the tail vein, followed at the development of the maximum blood pressure response, i.e., 30 s later, by phentolamine (15 mg kg(-1)). In the second model, the vasopressin V1 receptor agonist ornithine-vasopressin (ornipressin; 0.5 IU kg(-1), i.v.) was administered. The heart rate, mean arterial blood pressure and surface electrocardiogram (ECG, standard lead II) were registered simultaneously. As a measure of myocardial ischaemia, at 1 min after phentolamine or ornipressin administration, we found significant ST-segment depression, lasting for more than 10 or 5 min, respectively. Pretreatment (15 min, s.c.) with the vasopressin V1 receptor antagonist Mca1,Tyr(Me)2AVP (the Manning peptide; 0.02-0.2 microg kg(-1)) or the platelet-activating factor receptor antagonist ginkgolide B (BN 52021; 0.25-2.5 mg kg(-1)) alone caused a dose-dependent reduction of the ST-segment depression. Concurrent administration of the two antagonists in their threshold doses (0.02 microg kg(-1) and 0.25 mg kg(-1)) also attenuated the ST-segment depression in both models. Neither antagonist affected the blood pressure or heart rate changes throughout the studies. Our results suggest that endogenous vasopressin and platelet-activating factor interact synergistically in provoking myocardial ischaemia in vivo in experimental angina in the rat. |
| Databáze: | OpenAIRE |
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