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Effects of subtypes of adrenergic and angiotensinergic antagonists on the water and sodium intake induced by adrenaline injected into the paraventricular nucleus

dc.contributor.authorCarnargo, LAD
dc.contributor.authorSaad, W. A.
dc.contributor.authorCerri, Paulo Sérgio [UNESP]
dc.contributor.authorCamargo, GMPD
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:45:47Z
dc.date.available2014-05-20T13:45:47Z
dc.date.issued2003-12-24
dc.description.abstractThe present experiments were conducted to investigate die role of the alpha(1A)-, alpha(1B)-, beta(1)-, beta(2)-adrenoceptors, and the effects of losartan and CGP42112A (selective ligands of the AT(1) and AT(2) angiotensin receptors, respectively) on the water and sodium intake elicited by paraventricular nucleus (PVN) injection of adrenaline. Male Holtzman rats with a stainless steel cannula implanted into the PVN were used. The ingestion of water and sodium was determined in separate groups submitted to water deprivation or sodium depletion with the diuretic furosemide (20 mg/rat). 5-Methylurapidil (an alpha(1A)-adrenergic antagonist) and ICI-118,551 (a beta(2)-adrenergic antagonist) injected into the PVN produced a dose-dependent increase, whereas cyclazosin (an alpha(1B)-adrenergic antagonist) and atenolol (a beta(1)-adrenergic antagonist) do not affect the inhibitory effect of water intake induced by adrenaline. on the other hand, the PVN administration of adrenaline increased the sodium intake in a dose-dependent manner. Previous injection of the alpha(1A) and beta(1) antagonists decreased, whereas injection of the alpha(1B) and beta(2) antagonists increased the salt intake induced by adrenaline. In rats with several doses of adrenaline into PVN, the previous administration of losartan increased in a dose-dependent manner the inhibitory effect of adrenaline and decreased the salt intake induced by adrenaline, while PVN CGP42112A was without effect. These results indicate that both appetites are mediated primarily by brain AT(1) receptors. However, the doses of losartan were more effective when combined with the doses of CGP42112A than given alone p < 0.05, suggesting that the water and salt intake effects of PVN adrenaline may involve activation of multiple angiotensin II (ANG II) receptors subtypes. (C) 2003 Elsevier B.V. All rights reserved.en
dc.description.affiliationPaulista State Univ, UNESP, Sch Dent, Dept Physiol, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationPaulista State Univ, UNESP, Sch Dent, Dept Morphol, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationPaulista State Univ, UNESP, Sch Pharmaceut Sci, Dept Clin Anal, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUnespPaulista State Univ, UNESP, Sch Dent, Dept Physiol, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUnespPaulista State Univ, UNESP, Sch Dent, Dept Morphol, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUnespPaulista State Univ, UNESP, Sch Pharmaceut Sci, Dept Clin Anal, BR-14801903 Araraquara, SP, Brazil
dc.format.extent234-242
dc.identifierhttp://dx.doi.org/10.1016/j.brainres.2003.09.045
dc.identifier.citationBrain Research. Amsterdam: Elsevier B.V., v. 994, n. 2, p. 234-242, 2003.
dc.identifier.doi10.1016/j.brainres.2003.09.045
dc.identifier.issn0006-8993
dc.identifier.lattes3278495911207882
dc.identifier.orcid0000-0001-5756-5828
dc.identifier.urihttp://hdl.handle.net/11449/16139
dc.identifier.wosWOS:000187249600011
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofBrain Research
dc.relation.ispartofjcr3.125
dc.relation.ispartofsjr1,404
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectalpha- and beta-adrenergic antagonistspt
dc.subjectAT(1) and AT(2) antagonistspt
dc.subjectwater intakept
dc.subjectsodium intakept
dc.subjectparaventricular nucleuspt
dc.titleEffects of subtypes of adrenergic and angiotensinergic antagonists on the water and sodium intake induced by adrenaline injected into the paraventricular nucleusen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes3278495911207882[3]
unesp.author.orcid0000-0001-5756-5828[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt
unesp.departmentFisiologia e Patologia - FOARpt
unesp.departmentMorfologia - FOARpt

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