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Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings

The root of Ostericum koreanum Maximowicz has been used as a traditional medicine called “Kanghwal” in Korea (or “Qianghuo” in China). The purpose of this study was to investigate the vasorelaxant activity and mechanism of action of an ethanol extract of the O. koreanum root (EOK). We used isolated...

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Autores principales: Lee, Kyungjin, Park, Geunyong, Ham, Inhye, Yang, Gabsik, Lee, Mihwa, Bu, Youngmin, Kim, Hocheol, Choi, Ho-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800564/
https://www.ncbi.nlm.nih.gov/pubmed/24204390
http://dx.doi.org/10.1155/2013/350964
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author Lee, Kyungjin
Park, Geunyong
Ham, Inhye
Yang, Gabsik
Lee, Mihwa
Bu, Youngmin
Kim, Hocheol
Choi, Ho-Young
author_facet Lee, Kyungjin
Park, Geunyong
Ham, Inhye
Yang, Gabsik
Lee, Mihwa
Bu, Youngmin
Kim, Hocheol
Choi, Ho-Young
author_sort Lee, Kyungjin
collection PubMed
description The root of Ostericum koreanum Maximowicz has been used as a traditional medicine called “Kanghwal” in Korea (or “Qianghuo” in China). The purpose of this study was to investigate the vasorelaxant activity and mechanism of action of an ethanol extract of the O. koreanum root (EOK). We used isolated rat aortic rings to assess the effects of EOK on various vasorelaxant or vasoconstriction factors. EOK induced vasorelaxation in phenylephrine hydrochloride (PE) or KCl precontracted aortic rings in a concentration-dependent manner. However, the vasorelaxant effects of EOK on endothelium-intact aortic rings were reduced by pretreatment with L-NAME or methylene blue. In Ca(2+)-free Krebs-Henseleit solution, pretreatment with EOK (0.3 mg/mL) completely inhibited PE-induced constriction. In addition, EOK (0.3 mg/mL) also completely inhibited vasoconstriction induced by supplemental Ca(2+) in aortic rings that were precontracted with PE or KCl. Furthermore, the EOK-induced vasorelaxation in PE-contracted aortic rings was inhibited by preincubation with nifedipine. These results indicate that the vasorelaxant effects of EOK are responsible for the induction of NO formation from L-Arg and NO-cGMP pathways, blockage of the extracellular Ca(2+) entry via the receptor-operative Ca(2+) channel and voltage-dependent calcium channel, and blockage of sarcoplasmic reticulum Ca(2+) release via the inositol triphosphate pathway.
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spelling pubmed-38005642013-11-07 Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings Lee, Kyungjin Park, Geunyong Ham, Inhye Yang, Gabsik Lee, Mihwa Bu, Youngmin Kim, Hocheol Choi, Ho-Young Evid Based Complement Alternat Med Research Article The root of Ostericum koreanum Maximowicz has been used as a traditional medicine called “Kanghwal” in Korea (or “Qianghuo” in China). The purpose of this study was to investigate the vasorelaxant activity and mechanism of action of an ethanol extract of the O. koreanum root (EOK). We used isolated rat aortic rings to assess the effects of EOK on various vasorelaxant or vasoconstriction factors. EOK induced vasorelaxation in phenylephrine hydrochloride (PE) or KCl precontracted aortic rings in a concentration-dependent manner. However, the vasorelaxant effects of EOK on endothelium-intact aortic rings were reduced by pretreatment with L-NAME or methylene blue. In Ca(2+)-free Krebs-Henseleit solution, pretreatment with EOK (0.3 mg/mL) completely inhibited PE-induced constriction. In addition, EOK (0.3 mg/mL) also completely inhibited vasoconstriction induced by supplemental Ca(2+) in aortic rings that were precontracted with PE or KCl. Furthermore, the EOK-induced vasorelaxation in PE-contracted aortic rings was inhibited by preincubation with nifedipine. These results indicate that the vasorelaxant effects of EOK are responsible for the induction of NO formation from L-Arg and NO-cGMP pathways, blockage of the extracellular Ca(2+) entry via the receptor-operative Ca(2+) channel and voltage-dependent calcium channel, and blockage of sarcoplasmic reticulum Ca(2+) release via the inositol triphosphate pathway. Hindawi Publishing Corporation 2013 2013-09-24 /pmc/articles/PMC3800564/ /pubmed/24204390 http://dx.doi.org/10.1155/2013/350964 Text en Copyright © 2013 Kyungjin Lee 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
Lee, Kyungjin
Park, Geunyong
Ham, Inhye
Yang, Gabsik
Lee, Mihwa
Bu, Youngmin
Kim, Hocheol
Choi, Ho-Young
Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings
title Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings
title_full Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings
title_fullStr Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings
title_full_unstemmed Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings
title_short Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings
title_sort vasorelaxant effect of osterici radix ethanol extract on rat aortic rings
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800564/
https://www.ncbi.nlm.nih.gov/pubmed/24204390
http://dx.doi.org/10.1155/2013/350964
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