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Fundam Clin Pharmacol ; 14(4): 363-8, 2000.
Article in English | MEDLINE | ID: mdl-11030443

ABSTRACT

In vitro experiments were designed to assess the inhibitory effect of the thiazide diuretics methyclothiazide (MCTZ), the hydrochlorothiazide (HCTZ), and the thiazide-related diuretic indapamide (IND) on contractile responses to norepinephrine (NE) and arginine vasopressin (AVP) of aortic rings from spontaneously hypertensive rats (SHR) and normotensive Wistar Kyoto rats (WKY). Changes in the tension of aortic ring preparations were measured isometrically. MCTZ (10(-4) M) induced endothelium-dependent inhibition of the vasoconstrictor responses to NE and AVP only in aortas from SHR, and the maximal vasoconstrictive effect of NE and AVP was decreased by 59 +/- 11% and 32.3 +/- 13%, respectively. Indapamide (10(-4) M) also induced endothelium-dependent inhibition of the contractile response to AVP in aortic rings from SHR, and the maximal vasoconstrictive effect of AVP was decreased by 33 +/- 5%. In contrast, HCTZ did not inhibit the contractile response to either NE or AVP, even at the highest concentration. This study provides evidence that methyclothiazide and indapamide inhibit the contractile response induced by norepinephrine and/or arginine vasopressin on SHR aortic preparations via an endothelium-dependent mechanism.


Subject(s)
Antihypertensive Agents/pharmacology , Diuretics/pharmacology , Indapamide/pharmacology , Methyclothiazide/pharmacology , Muscle, Smooth, Vascular/drug effects , Sodium Chloride Symporter Inhibitors/pharmacology , Animals , Aorta/drug effects , Aorta/physiology , Arginine Vasopressin/administration & dosage , Arginine Vasopressin/pharmacology , Dose-Response Relationship, Drug , Endothelium, Vascular/physiology , Hydrochlorothiazide/pharmacology , In Vitro Techniques , Male , Muscle Contraction/drug effects , Muscle, Smooth, Vascular/physiology , Norepinephrine/administration & dosage , Norepinephrine/pharmacology , Rats , Rats, Inbred SHR , Rats, Inbred WKY , Vasoconstrictor Agents/administration & dosage , Vasoconstrictor Agents/pharmacology
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