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The effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin II administration
BACKGROUND: Hypertension is the most common disease in the world. In Iranian folk medicine, unripe grape juice has been used as antihypertention remedy, but no data is documented for this popular belief. This study was designed to determine the effect of unripe grape extract (UGE) on blood pressure...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685765/ https://www.ncbi.nlm.nih.gov/pubmed/23798878 http://dx.doi.org/10.4103/0974-8490.110511 |
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author | Nematbakhsh, Mehdi Zolfaghari, Behzad Eshraghi, Fatemeh Safari, Tahereh Pezeshki, Zahra Sorooshzadeh, Seyyed Mohammad-Ali |
author_facet | Nematbakhsh, Mehdi Zolfaghari, Behzad Eshraghi, Fatemeh Safari, Tahereh Pezeshki, Zahra Sorooshzadeh, Seyyed Mohammad-Ali |
author_sort | Nematbakhsh, Mehdi |
collection | PubMed |
description | BACKGROUND: Hypertension is the most common disease in the world. In Iranian folk medicine, unripe grape juice has been used as antihypertention remedy, but no data is documented for this popular belief. This study was designed to determine the effect of unripe grape extract (UGE) on blood pressure and the response to angiotensin II in rat. MATERIALS AND METHODS: Unripe grape was collected, air dried, and extracted and concentrated. Four groups of Wistar rats received single doses of 125, 250, and 500 mg/kg of UGE or saline, respectively. The direct blood pressure and the serum nitrite level were measured one hour post UGE administration. The animals also were subjected to the infusion of various angiotensin II concentrations (100, 300, and 1000 μg/kg/min), and blood pressure was determined. RESULTS: Mean arterial, systolic, and diastolic pressures (MAP, SP, and DP) in all UGE treated groups were less than the control group, but only at the dose of 125 mg/kg (Group 1) they were significantly different (P < 0.05). The level of nitrite in groups 1-3 were significantly greater than the control group (P < 0.05). No significant differences were detected for the MAP, SP, and DP to different concentrations of angiotensin II among these groups. CONCLUSION: UGE potentially attenuate MAP, SP, and DP via vasodilatation induced by nitric oxide production. |
format | Online Article Text |
id | pubmed-3685765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36857652013-06-24 The effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin II administration Nematbakhsh, Mehdi Zolfaghari, Behzad Eshraghi, Fatemeh Safari, Tahereh Pezeshki, Zahra Sorooshzadeh, Seyyed Mohammad-Ali Pharmacognosy Res Original Article BACKGROUND: Hypertension is the most common disease in the world. In Iranian folk medicine, unripe grape juice has been used as antihypertention remedy, but no data is documented for this popular belief. This study was designed to determine the effect of unripe grape extract (UGE) on blood pressure and the response to angiotensin II in rat. MATERIALS AND METHODS: Unripe grape was collected, air dried, and extracted and concentrated. Four groups of Wistar rats received single doses of 125, 250, and 500 mg/kg of UGE or saline, respectively. The direct blood pressure and the serum nitrite level were measured one hour post UGE administration. The animals also were subjected to the infusion of various angiotensin II concentrations (100, 300, and 1000 μg/kg/min), and blood pressure was determined. RESULTS: Mean arterial, systolic, and diastolic pressures (MAP, SP, and DP) in all UGE treated groups were less than the control group, but only at the dose of 125 mg/kg (Group 1) they were significantly different (P < 0.05). The level of nitrite in groups 1-3 were significantly greater than the control group (P < 0.05). No significant differences were detected for the MAP, SP, and DP to different concentrations of angiotensin II among these groups. CONCLUSION: UGE potentially attenuate MAP, SP, and DP via vasodilatation induced by nitric oxide production. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3685765/ /pubmed/23798878 http://dx.doi.org/10.4103/0974-8490.110511 Text en Copyright: © Pharmacognosy Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nematbakhsh, Mehdi Zolfaghari, Behzad Eshraghi, Fatemeh Safari, Tahereh Pezeshki, Zahra Sorooshzadeh, Seyyed Mohammad-Ali The effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin II administration |
title | The effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin II administration |
title_full | The effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin II administration |
title_fullStr | The effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin II administration |
title_full_unstemmed | The effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin II administration |
title_short | The effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin II administration |
title_sort | effects of unripe grape extract on systemic blood pressure, nitric oxide production, and response to angiotensin ii administration |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685765/ https://www.ncbi.nlm.nih.gov/pubmed/23798878 http://dx.doi.org/10.4103/0974-8490.110511 |
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