Planta Med 2006; 72(1): 78-81
DOI: 10.1055/s-2005-873179
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Inhibitory Effect of the Norlignan 2-(2′-Hydroxy-4′,6′-dimethoxyphenyl)-5-[(E)-propenyl]benzofuran from Krameria tomentosa on Acetylcholine-Induced Relaxation of the Rat Aorta

Janiza C. M. Castro1 , Marcelo S. Silva1 , Steyner F. Cortes2 , Virgínia S. Lemos3
  • 1Laboratório de Tecnologia Farmacêutica, Universidade Federal da Paraíba, João Pessoa, PB, Brazil
  • 2Departamento de Farmacologia - ICB, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
  • 3Departamento de Fisiologia e Biofísica - ICB, Universidade Federal de Minas Gerais. Belo Horizonte, Brazil
Further Information

Publication History

Received: March 16, 2005

Accepted: June 10, 2005

Publication Date:
10 November 2005 (online)

Abstract

In this work, we studied the effect of the norlignan 2-(2′-hydroxy-4′,6′-dimethoxyphenyl)-5-[(E)-propenyl]benzofuran (DMPP) in the rat aorta. In aortic rings with intact endothelium, DMPP inhibited in a concentration-dependent manner the vasodilator effect produced by acetylcholine with an IC50 value of 31.2 ± 6.3 μM. DMPP also inhibited basal nitric oxide production. In endothelium-denuded vessels DMPP was without effect whereas superoxide dismutase (SOD) was effective in potentiating responses to the NO donor SIN-1. Contractile effects of carbachol in guinea-pig ileum and trachea were unaffected by DMPP. It is concluded that DMPP inhibits the endothelium-dependent relaxation induced by acetylcholine in the rat aorta without affecting receptor or smooth muscle cells function. Decreased nitric oxide production by endothelial cells seems to be the mechanism involved in the inhibitory effect of DMPP.

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Virgínia S. Lemos

Departamento de Fisiologia e Biofísica

Universidade Federal de Minas Gerais

Av. Antônio Carlos 6627

31270-901, Belo Horizonte, MG

Brazil

Fax: +55-31-499-2924

Email: vslemos@mono.icb.ufmg.br

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