Cover image of the article: Vasorelaxatory Effect of Vitis vinifera Extract on Rat Aorta

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Vasorelaxatory Effect of Vitis vinifera Extract on Rat Aorta

Authors

Mohammadkazem Gharibnaseri1,*, Mojdeh Navid Hamidi1, Akbar Heidari2
1Department of Physiology, Medical School, Jondi Shapur Ahwaz University of Medical Sciences, Ahwaz, Iran
2School of Pharmacy, Jondi Shapur Ahwaz University of Medical Sciences, Ahwaz, Iran
*Corresponding Author: Department of Physiology, Medical School, Jondi Shapur Ahwaz University of Medical Sciences, Ahwaz, Iran. Email:gharibnaseri_m@yahoo.com

Iranian Journal of Pharmaceutical Research:Vol. 4, issue 2; 93-99
Published online:Nov 20, 2010
Article type:Research Article
Received:Nov 20, 2004
Accepted:Mar 20, 2005
How to Cite:Gharibnaseri M, Navid Hamidi M, Heidari A. Vasorelaxatory Effect of Vitis vinifera Extract on Rat Aorta. Iran J Pharm Res. 2022;4(2):e128231. doi: https://doi.org/10.22037/ijpr.2010.622

Abstract

Reports have shown the antioxidant, hypotensive, hypolipidemic and vasodilatory effects of grape (Vitis vinifera L.) seed extract. We have recently shown the relaxatory effect of grape leaf extract on rat uterus and reduction of frog heart rate and contractility. The aim of the present study was to investigate the relaxant effect of Vitis vinifera leaf hydroalcoholic extract (VLHE) on rat thoracic aorta contractions induced by phenylephrine and KCl and the role of aorta endothelium on this action. Rat aorta was removed and placed in an organ bath containing Krebs-Henseleit solution and aorta contractions were recorded isometrically.

The results demonstrate that VLHE (0.125-2 mg/ml) reduces the endothelial intact aorta reconstructed by phenylephrine (1 µM) dose-dependently (P<0.0001). Extract induced the same response in endothelial denuded aorta, but in a much lesser extent. The IC50 for both groups were 0.45±0.08 and 1.73±0.23 mg/ml, respectively. However, the contractile responses of these groups were similar. VLHE (0.125-2 mg/ml) reduced the contractions induced by KCl (80 mM) dose-dependently (P<0.0001). The relaxatory effect of VHLE on KCl–induced contractions was less than those evoked by Phenylephrine. Vasorelaxatory effect of VHLE on intact aorta was attenuated by nitric oxide synthase inhibitor (L-NAME, 100 µM) and gaunyl cyclase inhibitor (methylene blue, 10 µM) significantly, but was unaffected by atropine (1 µM).

The results suggest that the greatest vasorelaxant effect of VHLE on rat aorta is endothelium-dependent and nitric oxide (NO) and cGMP are mostly responsible but cholinergic receptors are not involved.

Highlights

Copyright

© 2022, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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