Please use this identifier to cite or link to this item: http://repositorio.unitau.br/jspui/handle/20.500.11874/2824
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dc.contributor.authorCamargo, Gabriela Maria Pavan de Arrudapt_BR
dc.contributor.authorCamargo, Luiz Antonio de Arrudapt_BR
dc.contributor.authorSaad, William Abraopt_BR
dc.date.accessioned2019-09-12T16:53:52Z-
dc.date.available2019-09-12T16:53:52Z-
dc.date.issued2009-
dc.citation.volume21pt_BR
dc.citation.issue2pt_BR
dc.citation.spage151-
dc.citation.epage154-
dc.identifier.doi10.1111/j.1365-2826.2008.01816.xpt_BR
dc.identifier.issn0953-8194-
dc.identifier.issn1365-2826-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/2824-
dc.description.abstractThe present study aimed to determine the effects of selective antagonists of V-1a, V-2, and V-1a/V-2 (Conivaptan; Astellas Pharma Inc., Tokyo, Japan) arginine vasopressin (AVP) receptors on the flow of urine and sodium excretion induced by AVP, by means of microinjections into the medial septal area (MSA) of the rat brain. Male Holtzman rats had a guide cannula implanted into the dorsal surface of the MSA. Intravenous infusion of hypotonic saline was used to promote urinary flow, which was collected for 4 h. Pretreatment with the V-1a antagonist decreased, and the V-2 antagonist and Conivaptan (a V-1a/V-2 antagonist) increased, the urinary flow induced by AVP. Administration of AVP increased sodium excretion. Pretreatment with V-2 or V-1a antagonists decreased, and Conivaptan abolished, the sodium excretion induced by AVP. These results indicate that the V-1a and V-2 receptors of the MSA are important in the central regulation of urine and sodium excretion.en
dc.description.provenanceMade available in DSpace on 2019-09-12T16:53:52Z (GMT). No. of bitstreams: 0 Previous issue date: 2009en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)pt_BR
dc.languageInglêspt_BR
dc.publisherWiley-
dc.publisher.countryEstados Unidospt_BR
dc.relation.ispartofJournal of Neuroendocrinology-
dc.rightsEm verificaçãopt_BR
dc.sourceWeb of Sciencept_BR
dc.subject.otherVasopressinen
dc.subject.otherMedial Septal Areaen
dc.subject.otherV-1a And V-2 Receptorsen
dc.subject.otherUrine Excretionen
dc.subject.otherSodium Excretionen
dc.subject.otherParaventricular Nucleusen
dc.subject.otherAngiotensin Receptorsen
dc.subject.otherAntagonisten
dc.subject.otherConivaptanen
dc.subject.otherWateren
dc.subject.otherV-1aen
dc.subject.otherEfficacyen
dc.subject.otherYmo87en
dc.subject.otherSiadhen
dc.subject.otherMsaen
dc.titleMedial Septal Area Vasopressin Receptor Subtypes in the Regulation of Urine and Sodium Excretion in Ratsen
dc.typeArtigo de Periódicopt_BR
dc.identifier.wosWOS:000262476900008-
dc.description.affiliation[de Arruda Camargo, G. M. P.] Sao Paulo State Univ, Dept Clin Anal, UNESP, Sao Paulo, Brazil-
dc.description.affiliation[de Arruda Camargo, L. A.; Saad, W. A.] Sao Paulo State Univ, Dept Physiol, UNESP, Sao Paulo, Brazil-
dc.description.affiliation[de Arruda Camargo, L. A.; Saad, W. A.] Univ Fed Sao Carlos, UFSCAR, Dept Physiol, BR-13560 Sao Carlos, Brazil-
dc.description.affiliation[Saad, W. A.] Universidade de Taubaté (Unitau), , Sao Paulo, Brazil-
dc.description.affiliation[Saad, W. A.] Univ Araraquara, UNIARA, Sao Paulo, Brazil-
dc.subject.wosareaEndocrinology & Metabolismen
dc.subject.wosareaNeurosciencesen
dc.subject.researchareaEndocrinology & Metabolismen
dc.subject.researchareaNeurosciences & Neurologyen
Appears in Collections:Artigos de Periódicos

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