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Vascular Reactivity Concerning Orthosiphon stamineus Benth-Mediated Antihypertensive in Aortic Rings of Spontaneously Hypertensive Rats
Orthosiphon stamineus Benth has been traditionally used to treat hypertension. The study aimed to investigate the vascular reactivity of water extract (WOS) and water : methanolic (1 : 1) extract (WMOS) of Orthosiphon stamineus Benth and AT(1) receptors blocker in the mechanisms of antihypertensive...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3710645/ https://www.ncbi.nlm.nih.gov/pubmed/23878738 http://dx.doi.org/10.1155/2013/456852 |
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author | Manshor, Nurul Maizan Dewa, Aidiahmad Asmawi, Mohd Zaini Ismail, Zhari Razali, Nadiah Hassan, Zurina |
author_facet | Manshor, Nurul Maizan Dewa, Aidiahmad Asmawi, Mohd Zaini Ismail, Zhari Razali, Nadiah Hassan, Zurina |
author_sort | Manshor, Nurul Maizan |
collection | PubMed |
description | Orthosiphon stamineus Benth has been traditionally used to treat hypertension. The study aimed to investigate the vascular reactivity of water extract (WOS) and water : methanolic (1 : 1) extract (WMOS) of Orthosiphon stamineus Benth and AT(1) receptors blocker in the mechanisms of antihypertensive mediated by α (1)-adrenergic receptor and EDNO and PGI(2) releases in the SHR aortic rings. SHR (230–280 g) were divided into four groups: control, WOS, WMOS, and losartan. After being fed orally for 14 days, the aorta was harvested and subjected to PE (10(−9) to 10(−5) M) and ACh (10(−9) to 10(−5) M) with and without L-NAME (100 µM) and indomethacin (10 µM), respectively. WOS, WMOS, and losartan significantly reduced the contractile responses to PE intact suggesting the importance of endothelium in vasorelaxation. Losartan significantly enhanced the ACh-induced vasorelaxation. L-NAME significantly inhibited the ACh-induced relaxation in all groups. Indomethacin enhanced ACh-induced vasorelaxation in WMOS. Collectively, Orthosiphon stamineus leaves extract reduced vasoconstriction responses by the alteration of α (1)-adrenergic and AT(1) receptors activities. The involvement of EDNO releases was clearly observed in this plant. In WOS, PGI(2) releases might not participate in the ACh-induced vasorelaxation. However, in WMOS, enhancement of vasorelaxation possibly due to continuous release of PGI(2). |
format | Online Article Text |
id | pubmed-3710645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37106452013-07-22 Vascular Reactivity Concerning Orthosiphon stamineus Benth-Mediated Antihypertensive in Aortic Rings of Spontaneously Hypertensive Rats Manshor, Nurul Maizan Dewa, Aidiahmad Asmawi, Mohd Zaini Ismail, Zhari Razali, Nadiah Hassan, Zurina Int J Vasc Med Research Article Orthosiphon stamineus Benth has been traditionally used to treat hypertension. The study aimed to investigate the vascular reactivity of water extract (WOS) and water : methanolic (1 : 1) extract (WMOS) of Orthosiphon stamineus Benth and AT(1) receptors blocker in the mechanisms of antihypertensive mediated by α (1)-adrenergic receptor and EDNO and PGI(2) releases in the SHR aortic rings. SHR (230–280 g) were divided into four groups: control, WOS, WMOS, and losartan. After being fed orally for 14 days, the aorta was harvested and subjected to PE (10(−9) to 10(−5) M) and ACh (10(−9) to 10(−5) M) with and without L-NAME (100 µM) and indomethacin (10 µM), respectively. WOS, WMOS, and losartan significantly reduced the contractile responses to PE intact suggesting the importance of endothelium in vasorelaxation. Losartan significantly enhanced the ACh-induced vasorelaxation. L-NAME significantly inhibited the ACh-induced relaxation in all groups. Indomethacin enhanced ACh-induced vasorelaxation in WMOS. Collectively, Orthosiphon stamineus leaves extract reduced vasoconstriction responses by the alteration of α (1)-adrenergic and AT(1) receptors activities. The involvement of EDNO releases was clearly observed in this plant. In WOS, PGI(2) releases might not participate in the ACh-induced vasorelaxation. However, in WMOS, enhancement of vasorelaxation possibly due to continuous release of PGI(2). Hindawi Publishing Corporation 2013 2013-06-26 /pmc/articles/PMC3710645/ /pubmed/23878738 http://dx.doi.org/10.1155/2013/456852 Text en Copyright © 2013 Nurul Maizan Manshor et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Manshor, Nurul Maizan Dewa, Aidiahmad Asmawi, Mohd Zaini Ismail, Zhari Razali, Nadiah Hassan, Zurina Vascular Reactivity Concerning Orthosiphon stamineus Benth-Mediated Antihypertensive in Aortic Rings of Spontaneously Hypertensive Rats |
title | Vascular Reactivity Concerning Orthosiphon stamineus Benth-Mediated Antihypertensive in Aortic Rings of Spontaneously Hypertensive Rats |
title_full | Vascular Reactivity Concerning Orthosiphon stamineus Benth-Mediated Antihypertensive in Aortic Rings of Spontaneously Hypertensive Rats |
title_fullStr | Vascular Reactivity Concerning Orthosiphon stamineus Benth-Mediated Antihypertensive in Aortic Rings of Spontaneously Hypertensive Rats |
title_full_unstemmed | Vascular Reactivity Concerning Orthosiphon stamineus Benth-Mediated Antihypertensive in Aortic Rings of Spontaneously Hypertensive Rats |
title_short | Vascular Reactivity Concerning Orthosiphon stamineus Benth-Mediated Antihypertensive in Aortic Rings of Spontaneously Hypertensive Rats |
title_sort | vascular reactivity concerning orthosiphon stamineus benth-mediated antihypertensive in aortic rings of spontaneously hypertensive rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3710645/ https://www.ncbi.nlm.nih.gov/pubmed/23878738 http://dx.doi.org/10.1155/2013/456852 |
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