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Interaction between paraventricular nucleus and medial septal area on the renal effects induced by adrenaline

dc.contributor.authorCamargo, LADA
dc.contributor.authorSaad, W. A.
dc.contributor.authorVilla, P. D.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.date.accessioned2014-05-20T13:45:47Z
dc.date.available2014-05-20T13:45:47Z
dc.date.issued2004-04-30
dc.description.abstractThe aim of the present study was to analyze the role of alpha(1),alpha(2)-adrenoceptors, and the effects of losartan and PD123319 (selective ligands of the AT(1) and AT(2) angiotensin receptors, respectively) injected into the paraventricular nucleus (PVN) on the diuresis, natriuresis, and kaliuresis induced by administration of adrenaline into the medial septal area (MSA). Male Holtzman rats with a stainless steel cannula implanted into the MSA and bilaterally into the PVN were used. The administration of adrenaline into the MSA increased in a dose-dependent manner the urine, sodium, and potassium excretions. The previous administration of prazosin (an alpha(1)-adrenoceptor antagonist) injected into the PVN abolished the above effects of adrenaline, whereas yohimbine (an a-adrenoceptor antagonist) doesn't affect the diuresis, natriuresis, and kaliuresis induced by adrenaline. Pretreatment with losartan into the PVN decreased in a dose-dependent manner the urine, sodium, and potassium excretions induced by MSA administration of adrenaline (50 ng), while PVN PD123319 was without effect. These results indicate that urinary and electrolyte excretion effects induced by adrenaline into the MSA are mediated primarily by PVN AT, receptors. However, the doses of losartan were more effective when combined with the doses of PD123319 than given alone, suggesting that the urinary, natriuretic, and kaliuretic effects of MSA adrenaline may involve activation of multiple angiotensin II receptors subtypes into the PVN. (C) 2004 Elsevier B.V All rights reserved.en
dc.description.affiliationUNESP, Sch Dent, Dept Physiol, BR-14801903 SP Araraquara, SP, Brazil
dc.description.affiliationUniv Fed Sao Carlos, Dept Physiol, BR-13560 Sao Carlos, SP, Brazil
dc.description.affiliationUnespUNESP, Sch Dent, Dept Physiol, BR-14801903 SP Araraquara, SP, Brazil
dc.format.extent135-139
dc.identifierhttp://dx.doi.org/10.1016/j.autneu.2004.01.003
dc.identifier.citationAutonomic Neuroscience-basic & Clinical. Amsterdam: Elsevier B.V., v. 111, n. 2, p. 135-139, 2004.
dc.identifier.doi10.1016/j.autneu.2004.01.003
dc.identifier.issn1566-0702
dc.identifier.urihttp://hdl.handle.net/11449/16141
dc.identifier.wosWOS:000222187700008
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofAutonomic Neuroscience-basic & Clinical
dc.relation.ispartofjcr2.605
dc.relation.ispartofsjr0,902
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectalpha(1) and alpha(2) receptorspt
dc.subjectAT(1) and AT(2) receptorspt
dc.subjecturinept
dc.subjectsodiumpt
dc.subjectpotassiumpt
dc.subjectmedial septal areapt
dc.subjectparaventricular nucleuspt
dc.titleInteraction between paraventricular nucleus and medial septal area on the renal effects induced by adrenalineen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublicationb3ba3d9c-022e-4521-8805-0bcceea7372e
relation.isDepartmentOfPublication.latestForDiscoveryb3ba3d9c-022e-4521-8805-0bcceea7372e
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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