Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain

Detalhes bibliográficos
Autor(a) principal: Saad, Wilson Abrão [UNESP]
Data de Publicação: 2006
Outros Autores: Guarda, I. F. M. S., Camargo, L. A. D. A. [UNESP], Guarda, R. S., Santos, T. A. F. B. D.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3923/jbs.2006.182.186
http://hdl.handle.net/11449/68736
Resumo: As several structures of the central nervous system are involved in the control of hydromineral and cardiovascular balance we investigated whether the natriorhexigenic and pressor response induced by the injection of ANG II into the 3rd V could be mediated by vasopressinergic and nitrergic system. Male Holtzman rats weighing 200-250 g with cannulae implanted into the 3rd V were used. The drugs were injected in 0.5 μL over 30-60 sec. Controls were injected with a similar volume of 0.15 M NaCl. ANGII increased the water intake vs control. AVPA injected into 3rd V prior to ANGII decreased the dipsogenic effect of ANGII. L-arginine also decreased the water intake induced by ANGII. AVPA plus L-arginine inhibit the water intake induced by ANGII. 7NIT injected prior to ANGII potentiated the dipsogenic effect of ANGII. Pre-treatment with ANGII increased the sodium ingestion vs control. AVPA decreased the ANGII effect in sodium intake. L-arginine also decreased the natriorhexigenic effect of ANGII. The combination of L-arginine and AVPA inhibit the sodium intake induced by ANGII. 7NIT injected prior to ANGII potentiated the sodium intake induced by ANGII. ANGII induced an increase in Mean Arterial Pressure (MAP) vs control. AVPA and L-arginine induced a decreased in the pressor effect of ANGII. The combination of L-arginine and AVPA inhibit the pressor effect of ANGII. 7NIT injected prior to ANGII into 3rd V potentiated the pressor effect of ANGII. These data suggest that arginine vasopressin V 1 receptors and Nitric Oxide (NO) within the circumventricular structures may be involved in sodium intake and pressor response induced by the activation of ANGII receptors within the circumventricular neurons. These studies revealed the involvement of sodium appetite by utilizing the angiotensinergic, vasopressinergic and nitrergic system in the central regulation of blood pressure. © 2006 Asian Network for Scientific Information.
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spelling Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brainANGII AVP V 1 receptorsCNSNOSodium appetite an blood pressure7 nitroindazoleangiotensin IIangiotensin receptorarginineargipressin receptornitric oxidesodium chloridewateranimal experimentanimal tissueblood pressure regulationbody weightbrain third ventriclecannulacontrolled studyenzyme activationfluid intakeinhibition kineticsmalemean arterial pressurenitrergic nervenonhumanpressor responseratrat strainsodium appetitesodium intakeAnimaliaAs several structures of the central nervous system are involved in the control of hydromineral and cardiovascular balance we investigated whether the natriorhexigenic and pressor response induced by the injection of ANG II into the 3rd V could be mediated by vasopressinergic and nitrergic system. Male Holtzman rats weighing 200-250 g with cannulae implanted into the 3rd V were used. The drugs were injected in 0.5 μL over 30-60 sec. Controls were injected with a similar volume of 0.15 M NaCl. ANGII increased the water intake vs control. AVPA injected into 3rd V prior to ANGII decreased the dipsogenic effect of ANGII. L-arginine also decreased the water intake induced by ANGII. AVPA plus L-arginine inhibit the water intake induced by ANGII. 7NIT injected prior to ANGII potentiated the dipsogenic effect of ANGII. Pre-treatment with ANGII increased the sodium ingestion vs control. AVPA decreased the ANGII effect in sodium intake. L-arginine also decreased the natriorhexigenic effect of ANGII. The combination of L-arginine and AVPA inhibit the sodium intake induced by ANGII. 7NIT injected prior to ANGII potentiated the sodium intake induced by ANGII. ANGII induced an increase in Mean Arterial Pressure (MAP) vs control. AVPA and L-arginine induced a decreased in the pressor effect of ANGII. The combination of L-arginine and AVPA inhibit the pressor effect of ANGII. 7NIT injected prior to ANGII into 3rd V potentiated the pressor effect of ANGII. These data suggest that arginine vasopressin V 1 receptors and Nitric Oxide (NO) within the circumventricular structures may be involved in sodium intake and pressor response induced by the activation of ANGII receptors within the circumventricular neurons. These studies revealed the involvement of sodium appetite by utilizing the angiotensinergic, vasopressinergic and nitrergic system in the central regulation of blood pressure. © 2006 Asian Network for Scientific Information.Department of Exacts and Naturals Sciences, Uiara, Araraquara São PauloInstitute of Bioscience UNITAU, Taubaté, SPDepartment of Physiology and Pathology School of Dentistry UNESP, 1680 Humaitá Street, Araraquara, SP 14801-903Department of Surgery School of Medicine University of São Paulo, São PauloPublic Medical Hospital, São PauloDepartment of Physiology and Pathology School of Dentistry UNESP, 1680 Humaitá Street, Araraquara, SP 14801-903Universidade de Taubaté (UNITAU)Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Saad, Wilson Abrão [UNESP]Guarda, I. F. M. S.Camargo, L. A. D. A. [UNESP]Guarda, R. S.Santos, T. A. F. B. D.2014-05-27T11:21:47Z2014-05-27T11:21:47Z2006-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article182-186http://dx.doi.org/10.3923/jbs.2006.182.186Journal of Biological Sciences, v. 6, n. 1, p. 182-186, 2006.1727-30481812-5719http://hdl.handle.net/11449/6873610.3923/jbs.2006.182.1862-s2.0-33644513409Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Biological Sciences0,1740,174info:eu-repo/semantics/openAccess2021-10-23T11:21:52Zoai:repositorio.unesp.br:11449/68736Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T11:21:52Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain
title Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain
spellingShingle Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain
Saad, Wilson Abrão [UNESP]
ANGII AVP V 1 receptors
CNS
NO
Sodium appetite an blood pressure
7 nitroindazole
angiotensin II
angiotensin receptor
arginine
argipressin receptor
nitric oxide
sodium chloride
water
animal experiment
animal tissue
blood pressure regulation
body weight
brain third ventricle
cannula
controlled study
enzyme activation
fluid intake
inhibition kinetics
male
mean arterial pressure
nitrergic nerve
nonhuman
pressor response
rat
rat strain
sodium appetite
sodium intake
Animalia
title_short Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain
title_full Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain
title_fullStr Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain
title_full_unstemmed Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain
title_sort Influence of arginine vasopressin receptor and nitric oxide on the water, sodium intake and arterial blood pressure induce by angiotensin injected into third ventricle of the brain
author Saad, Wilson Abrão [UNESP]
author_facet Saad, Wilson Abrão [UNESP]
Guarda, I. F. M. S.
Camargo, L. A. D. A. [UNESP]
Guarda, R. S.
Santos, T. A. F. B. D.
author_role author
author2 Guarda, I. F. M. S.
Camargo, L. A. D. A. [UNESP]
Guarda, R. S.
Santos, T. A. F. B. D.
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade de Taubaté (UNITAU)
Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Saad, Wilson Abrão [UNESP]
Guarda, I. F. M. S.
Camargo, L. A. D. A. [UNESP]
Guarda, R. S.
Santos, T. A. F. B. D.
dc.subject.por.fl_str_mv ANGII AVP V 1 receptors
CNS
NO
Sodium appetite an blood pressure
7 nitroindazole
angiotensin II
angiotensin receptor
arginine
argipressin receptor
nitric oxide
sodium chloride
water
animal experiment
animal tissue
blood pressure regulation
body weight
brain third ventricle
cannula
controlled study
enzyme activation
fluid intake
inhibition kinetics
male
mean arterial pressure
nitrergic nerve
nonhuman
pressor response
rat
rat strain
sodium appetite
sodium intake
Animalia
topic ANGII AVP V 1 receptors
CNS
NO
Sodium appetite an blood pressure
7 nitroindazole
angiotensin II
angiotensin receptor
arginine
argipressin receptor
nitric oxide
sodium chloride
water
animal experiment
animal tissue
blood pressure regulation
body weight
brain third ventricle
cannula
controlled study
enzyme activation
fluid intake
inhibition kinetics
male
mean arterial pressure
nitrergic nerve
nonhuman
pressor response
rat
rat strain
sodium appetite
sodium intake
Animalia
description As several structures of the central nervous system are involved in the control of hydromineral and cardiovascular balance we investigated whether the natriorhexigenic and pressor response induced by the injection of ANG II into the 3rd V could be mediated by vasopressinergic and nitrergic system. Male Holtzman rats weighing 200-250 g with cannulae implanted into the 3rd V were used. The drugs were injected in 0.5 μL over 30-60 sec. Controls were injected with a similar volume of 0.15 M NaCl. ANGII increased the water intake vs control. AVPA injected into 3rd V prior to ANGII decreased the dipsogenic effect of ANGII. L-arginine also decreased the water intake induced by ANGII. AVPA plus L-arginine inhibit the water intake induced by ANGII. 7NIT injected prior to ANGII potentiated the dipsogenic effect of ANGII. Pre-treatment with ANGII increased the sodium ingestion vs control. AVPA decreased the ANGII effect in sodium intake. L-arginine also decreased the natriorhexigenic effect of ANGII. The combination of L-arginine and AVPA inhibit the sodium intake induced by ANGII. 7NIT injected prior to ANGII potentiated the sodium intake induced by ANGII. ANGII induced an increase in Mean Arterial Pressure (MAP) vs control. AVPA and L-arginine induced a decreased in the pressor effect of ANGII. The combination of L-arginine and AVPA inhibit the pressor effect of ANGII. 7NIT injected prior to ANGII into 3rd V potentiated the pressor effect of ANGII. These data suggest that arginine vasopressin V 1 receptors and Nitric Oxide (NO) within the circumventricular structures may be involved in sodium intake and pressor response induced by the activation of ANGII receptors within the circumventricular neurons. These studies revealed the involvement of sodium appetite by utilizing the angiotensinergic, vasopressinergic and nitrergic system in the central regulation of blood pressure. © 2006 Asian Network for Scientific Information.
publishDate 2006
dc.date.none.fl_str_mv 2006-01-01
2014-05-27T11:21:47Z
2014-05-27T11:21:47Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3923/jbs.2006.182.186
Journal of Biological Sciences, v. 6, n. 1, p. 182-186, 2006.
1727-3048
1812-5719
http://hdl.handle.net/11449/68736
10.3923/jbs.2006.182.186
2-s2.0-33644513409
url http://dx.doi.org/10.3923/jbs.2006.182.186
http://hdl.handle.net/11449/68736
identifier_str_mv Journal of Biological Sciences, v. 6, n. 1, p. 182-186, 2006.
1727-3048
1812-5719
10.3923/jbs.2006.182.186
2-s2.0-33644513409
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Biological Sciences
0,174
0,174
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 182-186
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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