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Involvement of the 5-HT(1A) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions
OBJECTIVE(S): The 5-hydroxytryptamine1A (5-HT(1A)) receptor is one of the serotonin receptors in the brain, which regulates cardiovascular responses, especially in hemorrhage. Presence of this receptor in the cuneiform nucleus (CnF) has been shown. The present study evaluates the cardiovascular effe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Mashhad University of Medical Sciences
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395185/ https://www.ncbi.nlm.nih.gov/pubmed/32774806 http://dx.doi.org/10.22038/ijbms.2020.40453.9579 |
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author | Mohebbati, Reza Hosseini, Mahmoud Khazaei, Majid Khajavi Rad, Abolfazl Shafei, Mohammad Naser |
author_facet | Mohebbati, Reza Hosseini, Mahmoud Khazaei, Majid Khajavi Rad, Abolfazl Shafei, Mohammad Naser |
author_sort | Mohebbati, Reza |
collection | PubMed |
description | OBJECTIVE(S): The 5-hydroxytryptamine1A (5-HT(1A)) receptor is one of the serotonin receptors in the brain, which regulates cardiovascular responses, especially in hemorrhage. Presence of this receptor in the cuneiform nucleus (CnF) has been shown. The present study evaluates the cardiovascular effect of this receptor of the CnF in normal and hypotensive hemorrhagic rats. MATERIALS AND METHODS: Agonist (8-OH-DPAT) and antagonist (WAY-100635) of 5-HT(1A) microinjected into the CnF in basal and hemorrhagic conditions and cardiovascular responses were evaluated. Hemorrhage induced by blood withdrawal from the femoral artery and 2 min after that drugs microinjected. Time course and peak changes (∆) of the mean arterial pressure (MAP), systolic blood pressure (SBP) and heart rate (∆HR) were obtained and compared to the control and hemorrhage groups. RESULTS: In basal condition, 8-OH-DPAT significantly decreased ∆SBP, ∆MAP and ∆HR compared to the control (P<0.05-P<0.01), while way-100635 did not have a significant effect. Hypotension and tachycardia induced by hemorrhage ameliorated by agonist (P<0.05-P<0.01), while antagonist deteriorated hypotension (P<0.05) but attenuated tachycardia (P<0.01). CONCLUSION: This study shows that 5-HT(1A) receptor of the CnF involves in regulation of the cardiovascular responses. However, this effect in basal and hemorrhage conditions is different. |
format | Online Article Text |
id | pubmed-7395185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-73951852020-08-07 Involvement of the 5-HT(1A) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions Mohebbati, Reza Hosseini, Mahmoud Khazaei, Majid Khajavi Rad, Abolfazl Shafei, Mohammad Naser Iran J Basic Med Sci Original Article OBJECTIVE(S): The 5-hydroxytryptamine1A (5-HT(1A)) receptor is one of the serotonin receptors in the brain, which regulates cardiovascular responses, especially in hemorrhage. Presence of this receptor in the cuneiform nucleus (CnF) has been shown. The present study evaluates the cardiovascular effect of this receptor of the CnF in normal and hypotensive hemorrhagic rats. MATERIALS AND METHODS: Agonist (8-OH-DPAT) and antagonist (WAY-100635) of 5-HT(1A) microinjected into the CnF in basal and hemorrhagic conditions and cardiovascular responses were evaluated. Hemorrhage induced by blood withdrawal from the femoral artery and 2 min after that drugs microinjected. Time course and peak changes (∆) of the mean arterial pressure (MAP), systolic blood pressure (SBP) and heart rate (∆HR) were obtained and compared to the control and hemorrhage groups. RESULTS: In basal condition, 8-OH-DPAT significantly decreased ∆SBP, ∆MAP and ∆HR compared to the control (P<0.05-P<0.01), while way-100635 did not have a significant effect. Hypotension and tachycardia induced by hemorrhage ameliorated by agonist (P<0.05-P<0.01), while antagonist deteriorated hypotension (P<0.05) but attenuated tachycardia (P<0.01). CONCLUSION: This study shows that 5-HT(1A) receptor of the CnF involves in regulation of the cardiovascular responses. However, this effect in basal and hemorrhage conditions is different. Mashhad University of Medical Sciences 2020-07 /pmc/articles/PMC7395185/ /pubmed/32774806 http://dx.doi.org/10.22038/ijbms.2020.40453.9579 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Mohebbati, Reza Hosseini, Mahmoud Khazaei, Majid Khajavi Rad, Abolfazl Shafei, Mohammad Naser Involvement of the 5-HT(1A) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions |
title | Involvement of the 5-HT(1A) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions |
title_full | Involvement of the 5-HT(1A) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions |
title_fullStr | Involvement of the 5-HT(1A) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions |
title_full_unstemmed | Involvement of the 5-HT(1A) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions |
title_short | Involvement of the 5-HT(1A) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions |
title_sort | involvement of the 5-ht(1a) receptor of the cuneiform nucleus in the regulation of cardiovascular responses during normal and hemorrhagic conditions |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395185/ https://www.ncbi.nlm.nih.gov/pubmed/32774806 http://dx.doi.org/10.22038/ijbms.2020.40453.9579 |
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