Khan, A. and Ullah, R. and Mustafa, Mohd Rais and Hussain, J. and Murugan, D.D. and Hadi, A.H.B.A. (2012) Vasodilator effect of phlomis bracteosa constituents is mediated through dual Endothelium-Dependent and Endothelium-Independent pathways. Clinical and Experimental Hypertension, 34 (2). pp. 132-139. ISSN 1064-1963, DOI https://doi.org/10.3109/10641963.2011.601383.
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Abstract
This study describes the vasorelaxant potential of some pure compounds isolated from Phlomis bracteosa L.: marrubiin, phlomeoic acid, and two new constituents labeled as RA and RB. In rat thoracic aortic rings denuded of endothelium, marrubiin, phlomeoic acid, RA, and RB caused relaxation of high K+ (80 mM) and phenylephrine (1 ìM)-induced contractions at the concentration range of 1.0�1000 ìg/mL. Marrubiin, phlomeoic acid, RA, and RB concentration dependently (3.0�10 ìg/mL) shifted the Ca++ curves to the right obtained in Ca++-free medium. The vasodilator effect of marrubiin, phlomeoic acid, RA, and RB was partially blocked by Nù-nitro-L-arginine methyl ester in endotheliumintact aorta preparations. These results reveal that P. bracteosa constituents: marrubiin, phlomeoic acid, RA, and RB exhibit vasodilator action occurred via a combination of endothelium-independent Ca++ antagonism and endotheliumdependent Nù-nitro-L-arginine methyl ester-sensitive nitric oxide-modulating mechanism.
Item Type: | Article |
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Funders: | UNSPECIFIED |
Additional Information: | Address correspondence to Arif-ullah Khan, Center for Natural Products Research and Drug Discovery, Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia. E-mail: arifullahkhan979asia@yahoo.com |
Uncontrolled Keywords: | Phlomis bracteosa compounds, vasodilatation, Ca++ channel inhibition, nitric oxide modulation |
Subjects: | R Medicine |
Divisions: | Faculty of Medicine |
Depositing User: | Ms Haslinda Lahuddin |
Date Deposited: | 12 Jun 2012 04:08 |
Last Modified: | 18 Dec 2019 06:40 |
URI: | http://eprints.um.edu.my/id/eprint/3294 |
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