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Involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats

BACKGROUND: Arterial baroreflex (ABR) is an important factor in preventing of blood pressure fluctuations that determined by baroreflex sensitivity (BRS). Estrogen is an ovarian hormone that has influence on ABR. The mechanism of this effect of estrogen unknown and may be mediated by β-adrenergic re...

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Autores principales: Pourshanazari, Ali Asghar, Mohagheghi, Ozra, Pilavarian, Ali A., Enayatfard, Lili, Shafei, Mohammad N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988600/
https://www.ncbi.nlm.nih.gov/pubmed/24761391
http://dx.doi.org/10.4103/2277-9175.127996
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author Pourshanazari, Ali Asghar
Mohagheghi, Ozra
Pilavarian, Ali A.
Enayatfard, Lili
Shafei, Mohammad N.
author_facet Pourshanazari, Ali Asghar
Mohagheghi, Ozra
Pilavarian, Ali A.
Enayatfard, Lili
Shafei, Mohammad N.
author_sort Pourshanazari, Ali Asghar
collection PubMed
description BACKGROUND: Arterial baroreflex (ABR) is an important factor in preventing of blood pressure fluctuations that determined by baroreflex sensitivity (BRS). Estrogen is an ovarian hormone that has influence on ABR. The mechanism of this effect of estrogen unknown and may be mediated by β-adrenergic receptor of nucleus tractus solitarius (NTS), an important area in regulation of baroreflex. Therefore, in this study changing of BRS by estrogen after blockade β-adrenergic receptor of NTS in ovariectomized rats (Ovx) and Ovx treated with estrogen (Est) was examined. MATERIALS AND METHODS: After ovariectomy, all female rats divided to Ovx and Ovx + Est groups and two series of experiments were performed. In the first experiment, phenylephrine was [intravenously, IV] injected in both the Ovx and Ovx + Est groups, and mean arterial pressure (MAP), heart rate (HR), and BRS were evaluated (n = 8 for each group). In the second experiment, each of Ovx and Ovx + Est groups divided into saline and propranolol (pro) groups, saline and pro stereotaxically were microinjected into NTS, respectively. Further, phenylephrine (IV) was injected in all groups and BRS was evaluated. RESULTS: BRS significantly increased in estrogen-treated groups (Ovx + Est) compared to Ovx groups (P < 0.01). The blockade β-adrenergic receptor of NTS by pro did not significantly changed BRS in both Ovx and Ovx + Est groups. CONCLUSION: We concluded that there aren’t any intraction between estrogen and β-adrenergic receptor of NTS in BRS.
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spelling pubmed-39886002014-04-23 Involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats Pourshanazari, Ali Asghar Mohagheghi, Ozra Pilavarian, Ali A. Enayatfard, Lili Shafei, Mohammad N. Adv Biomed Res Original Article BACKGROUND: Arterial baroreflex (ABR) is an important factor in preventing of blood pressure fluctuations that determined by baroreflex sensitivity (BRS). Estrogen is an ovarian hormone that has influence on ABR. The mechanism of this effect of estrogen unknown and may be mediated by β-adrenergic receptor of nucleus tractus solitarius (NTS), an important area in regulation of baroreflex. Therefore, in this study changing of BRS by estrogen after blockade β-adrenergic receptor of NTS in ovariectomized rats (Ovx) and Ovx treated with estrogen (Est) was examined. MATERIALS AND METHODS: After ovariectomy, all female rats divided to Ovx and Ovx + Est groups and two series of experiments were performed. In the first experiment, phenylephrine was [intravenously, IV] injected in both the Ovx and Ovx + Est groups, and mean arterial pressure (MAP), heart rate (HR), and BRS were evaluated (n = 8 for each group). In the second experiment, each of Ovx and Ovx + Est groups divided into saline and propranolol (pro) groups, saline and pro stereotaxically were microinjected into NTS, respectively. Further, phenylephrine (IV) was injected in all groups and BRS was evaluated. RESULTS: BRS significantly increased in estrogen-treated groups (Ovx + Est) compared to Ovx groups (P < 0.01). The blockade β-adrenergic receptor of NTS by pro did not significantly changed BRS in both Ovx and Ovx + Est groups. CONCLUSION: We concluded that there aren’t any intraction between estrogen and β-adrenergic receptor of NTS in BRS. Medknow Publications & Media Pvt Ltd 2014-02-28 /pmc/articles/PMC3988600/ /pubmed/24761391 http://dx.doi.org/10.4103/2277-9175.127996 Text en Copyright: © 2014 Pourshanazari. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Pourshanazari, Ali Asghar
Mohagheghi, Ozra
Pilavarian, Ali A.
Enayatfard, Lili
Shafei, Mohammad N.
Involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats
title Involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats
title_full Involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats
title_fullStr Involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats
title_full_unstemmed Involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats
title_short Involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats
title_sort involvement of β-adrenergic receptor of nucleus tractus solitarius in changing of baroreflex sensitivity by estrogen in female rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988600/
https://www.ncbi.nlm.nih.gov/pubmed/24761391
http://dx.doi.org/10.4103/2277-9175.127996
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