Please use this identifier to cite or link to this item: http://repositorio.unitau.br/jspui/handle/20.500.11874/2630
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dc.contributor.authorSaad, Wilson Abraopt_BR
dc.contributor.authorCamargo, Luiz Antonio de Arrudapt_BR
dc.contributor.authorCerri, Paulo Sérgiopt_BR
dc.contributor.authorSimões, Silviopt_BR
dc.contributor.authorGarcia, Gustavopt_BR
dc.contributor.authorGutierrez, Laura Izabelpt_BR
dc.contributor.authorGuarda, Ismaelpt_BR
dc.contributor.authorGuarda, Renata Saadpt_BR
dc.contributor.authorSaad, William Abrãopt_BR
dc.date.accessioned2019-09-12T16:53:34Z-
dc.date.available2019-09-12T16:53:34Z-
dc.date.issued2004-
dc.citation.volume111pt_BR
dc.citation.issue1pt_BR
dc.citation.spage66-
dc.citation.epage70-
dc.identifier.doi10.1016/j.autneu.2003.08.013pt_BR
dc.identifier.issn1566-0702-
dc.identifier.issn1872-7484-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/2630-
dc.description.abstractIn this study we investigated the influence of d(CH2)(5)-Tyr(Me)-[Arg(8)]vasopressin (AAVP) and [adamanteanacetyl(1),0-ET-DTyr(2), Val(4), aminobutyryl(6), Arg(8,9)]-[Arg(8)]vasopressin (ATAVP), which are antagonists of vasopressin V-1 and V-2 receptors, and the effects of losartan, a selective angiotensin AT(1) receptor antagonist, and CGP42112A, a selective AT(2) receptor antagonist, injected into the lateral septal area (LSA) on thirst and hypertension induced by [Arg(8)]vasopressin (AVP). AAVP and ATAVP injected into the LSA reduced the drinking responses elicited by injecting AVP into the LSA. Both the AT(1) and AT(2) ligands administered into the LSA elicited a concentration-dependent decrease in the water intake induced by AVP injected into the LSA, but losartan was more effective than CGP42112A. The increase in MAP, due to injection of AVP into the LSA, was reduced by prior injection of AAVP from 18 +/- 1 to 6 +/- 1 mm Hg. Losartan injected into the LSA prior to AVP reduced the increase in MAP to 7 +/- 0.8 mm Hg. ATAVP and CGP42112A produced no changes in the pressor effect of AVP. These results suggest that the dipsogenic effects induced by injecting AVP into the LSA were mediated primarily by AT(1) receptors. However, doses of losartan were more effective when combined with CGP42112A than when given alone, suggesting that the thirst induced by AVP injections into LSA may involve activation of multiple AVP and angiotensin II receptor subtypes. The pressor response of AVP was reduced by losartan and by AAVP. CGP42112A and ATAVP did not change the AVP pressor response. These results suggest that facilitator effects of AVP on water intake are mediated through the activation of V-1 receptors and that the inhibitory effect requires V-2 receptors. The involvement of AT(1) and AT(2) receptors can be postulated. Based on the present findings, we suggest that the AVP in the LSA may play a role in the control of water and arterial blood pressure balance. (C) 2004 Elsevier B.V. All rights reserved.en
dc.description.provenanceMade available in DSpace on 2019-09-12T16:53:34Z (GMT). No. of bitstreams: 0 Previous issue date: 2004en
dc.languageInglêspt_BR
dc.publisherElsevier Science Bv-
dc.publisher.countryHolandapt_BR
dc.relation.ispartofAutonomic Neuroscience-Basic & Clinical-
dc.rightsAcesso Restritopt_BR
dc.sourceWeb of Sciencept_BR
dc.subject.otherVasopressinen
dc.subject.otherAntagonist V-1en
dc.subject.otherAntagonist V-2en
dc.subject.otherAngiotensin Receptor Subtypesen
dc.subject.otherWater Intakeen
dc.subject.otherArterial Pressureen
dc.subject.otherLateral Septal Areaen
dc.subject.otherBinding-Sitesen
dc.subject.otherSalt Appetiteen
dc.subject.otherBrainen
dc.subject.otherNeuronsen
dc.subject.otherLocalizationen
dc.subject.otherExcretionen
dc.subject.otherOxytocinen
dc.subject.otherDrinkingen
dc.subject.otherBlockadeen
dc.subject.otherPathwaysen
dc.titleInfluence of arginine vasopressin receptors and angiotensin receptor subtypes on the water intake and arterial blood pressure induced by vasopressin injected into the lateral septal area of the raten
dc.typeArtigo de Periódicopt_BR
dc.contributor.orcidCerri, Paulo https://orcid.org/0000-0001-5756-5828pt_BR
dc.contributor.researcheridCerri, Paulo/F-5338-2012pt_BR
dc.identifier.wosWOS:000221315700008-
dc.description.affiliationPaulista State Univ, Sch Dent, Dept Physiol, BR-14801903 Araraquara, SP, Brazil; , Dept Dent; State Univ, UNESP, UNIARA, Sch Dent Paulista,Dept Morphol, Araraquara, SP, Brazil-
dc.subject.wosareaNeurosciencesen
dc.subject.researchareaNeurosciences & Neurologyen
Appears in Collections:Artigos de Periódicos

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