Planta Med 2002; 68(4): 322-325
DOI: 10.1055/s-2002-26755
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Inhibitory Effect of N(G)-Nitro-L-arginine Methyl Ester on the Anti-Adrenergic Response Elicited by Ayanin in the Pithed Rat

M. F. Guerrero1, 3 , P. Puebla2 , M. L. Martín1 , R. Carrón1 , L. San Román1 , M. T. Reguero3 , L. Arteaga3
  • 1Laboratorio de Farmacognosia y Farmacología, Departamento de Fisiología y Farmacología, Facultad de Farmacia, Universidad de Salamanca, Salamanca, Spain
  • 2Departamento de Química Farmacéutica, Facultad de Farmacia, Universidad de Salamanca, Salamanca, Spain
  • 3Departamento de Farmacia, Facultad de Ciencias, Universidad Nacional de Colombia, Bogotá, Colombia
Further Information

Publication History

June 13, 2001

October 20, 2001

Publication Date:
02 May 2002 (online)

Abstract

In this study we evaluated the anti-adrenergic response elicited by ayanin, a flavonoid compound isolated from Croton schiedeanus Schlecht, in the pithed rat, and the inhibitory effect of NO synthase inhibitor N(G)-nitro-L-arginine methyl ester (L-NAME), and its acute toxicity profile in mice. In pithed rats ayanin (5 - 50 mg/kg i. v.) caused a dose-dependent decrease in the pressor and chronotropic responses induced by intravenous noradrenaline administration (0.25 μg/kg). This anti-adrenergic response was completely abolished by prior treatment with L-NAME (10 mg/kg i.v ) and the inhibitory effect of L-NAME was reversed after intravenous administration of L-arginine (100 mg/kg, i. v.). No lethal or major toxic effects were observed in mice receiving i. p. administration of ayanin up to a dose of 500 mg/kg. Our findings confirm that ayanin exerts protective cardiovascular effects against the increase in blood pressure and heart rate mainly through a mechanism that depends on the NO/cyclic guanosine monophosphate (cGMP) pathway without acute toxic effects. These results suggest that extracts of Croton schiedeanus, the native south American plant from which ayanin was isolated, might be beneficial in cardiovascular disease.

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M. L. Martín

Laboratorio de Farmacognosia y Farmacología

Departamento de Fisiología y Farmacología

Facultad de Farmacia

Universidad de Salamanca

37007 Salamanca

Spain

Phone: +34-923-294-530

Fax: +34-923-294-515

Email: marisam@usal.es

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