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Cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats

OBJECTIVE(S): Nitric oxide (NO) is an important neurotransmitter in central nervous system involved in central cardiovascular regulation. The presence of NO in the pedunculopontine tegmental (PPT) nucleus has been shown, but its cardiovascular effect has not been determined. In the present study, th...

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Autores principales: Shafei, Mohammad Naser, Nikyar, Tahereh, Hosseini, Mahmoud, Niazmand, Saeed, Paseban, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569585/
https://www.ncbi.nlm.nih.gov/pubmed/28852442
http://dx.doi.org/10.22038/IJBMS.2017.9009
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author Shafei, Mohammad Naser
Nikyar, Tahereh
Hosseini, Mahmoud
Niazmand, Saeed
Paseban, Maryam
author_facet Shafei, Mohammad Naser
Nikyar, Tahereh
Hosseini, Mahmoud
Niazmand, Saeed
Paseban, Maryam
author_sort Shafei, Mohammad Naser
collection PubMed
description OBJECTIVE(S): Nitric oxide (NO) is an important neurotransmitter in central nervous system involved in central cardiovascular regulation. The presence of NO in the pedunculopontine tegmental (PPT) nucleus has been shown, but its cardiovascular effect has not been determined. In the present study, the cardiovascular effect of NO in the PPT nucleus was evaluated. MATERIALS AND METHODS: After induction of anesthesia, a polyethylene catheter (PE-50) filled with heparinized saline inserted into the femoral artery, and the blood pressure (BP) and heart rate (HR) were continuously recorded. Animals were then placed in a stereotaxic apparatus and maximum changes of mean arterial pressure (∆MAP) and heart rate (∆HR) after microinjection of two doses of N(G)-nitro-L-arginine methyl ester (L-NAME, 30 and 90 nmol), L-arginine (L-Arg 10 and 50 nmol) and sodium nitroprusside (SNP, 9 and 27 nmol) into the PPT were provided and compared with control group (One-way ANOVA). RESULTS: Both doses of L-NAME significantly increased ∆MAP compared to control (P<0.05 and P<0.01, respectively). ∆HR only in higher dose (90 nmol) significantly increased compared to control (P<0.05). Two doses of L-Arg (10 and 50 nmol/150 nl) had no significant effect on ∆MAP or ∆HR. Higher dose of SNP (27 nmol) significantly decreased ∆MAP (P<0.05) and its both doses significantly decreased ∆HR compared to control (P<0.05 and P<0.001, respectively). Effect of higher dose on ∆HR was significantly higher than the lower dose (P<0.05). CONCLUSION: Our results show an inhibitory effect of the nitrergic system of the PPT on central cardiovascular system.
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spelling pubmed-55695852017-08-29 Cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats Shafei, Mohammad Naser Nikyar, Tahereh Hosseini, Mahmoud Niazmand, Saeed Paseban, Maryam Iran J Basic Med Sci Original Article OBJECTIVE(S): Nitric oxide (NO) is an important neurotransmitter in central nervous system involved in central cardiovascular regulation. The presence of NO in the pedunculopontine tegmental (PPT) nucleus has been shown, but its cardiovascular effect has not been determined. In the present study, the cardiovascular effect of NO in the PPT nucleus was evaluated. MATERIALS AND METHODS: After induction of anesthesia, a polyethylene catheter (PE-50) filled with heparinized saline inserted into the femoral artery, and the blood pressure (BP) and heart rate (HR) were continuously recorded. Animals were then placed in a stereotaxic apparatus and maximum changes of mean arterial pressure (∆MAP) and heart rate (∆HR) after microinjection of two doses of N(G)-nitro-L-arginine methyl ester (L-NAME, 30 and 90 nmol), L-arginine (L-Arg 10 and 50 nmol) and sodium nitroprusside (SNP, 9 and 27 nmol) into the PPT were provided and compared with control group (One-way ANOVA). RESULTS: Both doses of L-NAME significantly increased ∆MAP compared to control (P<0.05 and P<0.01, respectively). ∆HR only in higher dose (90 nmol) significantly increased compared to control (P<0.05). Two doses of L-Arg (10 and 50 nmol/150 nl) had no significant effect on ∆MAP or ∆HR. Higher dose of SNP (27 nmol) significantly decreased ∆MAP (P<0.05) and its both doses significantly decreased ∆HR compared to control (P<0.05 and P<0.001, respectively). Effect of higher dose on ∆HR was significantly higher than the lower dose (P<0.05). CONCLUSION: Our results show an inhibitory effect of the nitrergic system of the PPT on central cardiovascular system. Mashhad University of Medical Sciences 2017-07 /pmc/articles/PMC5569585/ /pubmed/28852442 http://dx.doi.org/10.22038/IJBMS.2017.9009 Text en Copyright: © Iranian Journal of Basic Medical Sciences 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
Shafei, Mohammad Naser
Nikyar, Tahereh
Hosseini, Mahmoud
Niazmand, Saeed
Paseban, Maryam
Cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats
title Cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats
title_full Cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats
title_fullStr Cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats
title_full_unstemmed Cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats
title_short Cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats
title_sort cardiovascular effects of nitrergic system of the pedunculopontine tegmental nucleus in anesthetized rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569585/
https://www.ncbi.nlm.nih.gov/pubmed/28852442
http://dx.doi.org/10.22038/IJBMS.2017.9009
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