Please use this identifier to cite or link to this item: http://repositorio.unitau.br/jspui/handle/20.500.11874/1872
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dc.contributor.authorSaad, Wilson Abraopt_BR
dc.contributor.authorGuarda, Ismael Francisco Motta Sigueirapt_BR
dc.contributor.authorCarmago, Luis Antonio de Arrudapt_BR
dc.contributor.authorSantos, Talmir Augusto Faria Brizola dospt_BR
dc.contributor.authorSaad, William Abrãopt_BR
dc.date.accessioned2019-09-12T16:26:07Z-
dc.date.available2019-09-12T16:26:07Z-
dc.date.issued2007-
dc.citation.volume7pt_BR
dc.citation.issue5pt_BR
dc.citation.spage806-
dc.citation.epage810-
dc.identifier.doi10.3923/jbs.2007.806.810pt_BR
dc.identifier.issn17273048-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-34948897022&doi=10.3923%2fjbs.2007.806.810&partnerID=40&md5=588fe8c2d93a7ffd28a6d42a25a41403-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/1872-
dc.description.abstractWe study the effects of angiotensin receptors antagonists, arginine vasopressin receptor antagonist, L-arginine and L-NAME, injected into supraoptic nucleus of the hypothalamus (SON) on sodium intake induced by the injection of angiotensin II (ANGII). Holtzman rats weighing 200-250 g with canulae implanted into the SON were used. The drugs were injected in 0.5 μL over 30-60 sec. Sodium intake after injection of saline SAL+SAL 0.15 M NaCl was 0.10±00.1 mL 2 h-1; SAL+ANGII injected into SON increased sodium intake. Losartan injected prior to ANGII into SON decreased sodium intake induced by ANGII. PD123319 injected prior to ANGII produced no changes in sodium intake induced by ANGII. AVPA receptor V1 antagonist injected prior to ANGII reduced sodium intake with a less intensity than losartan. L-arginine injected prior to ANGII decreases sodium intake at a same intensity than losartan. L-NAME injected prior to ANGII potentiated sodium intake induced by ANGII. Losartan injected simultaneously with L-arginine prior to ANGII blocked the natriorexigenic effect of ANGII. These results confirm the importance of SON in the control of sodium intake. Also suggest that both AT1 and arginine vasopressin V1 receptors interact with nitrergic pathways within the SON influencing the sodium metabolism by changing sodium appetite induced by ANGII. © 2007 Asian Network for Scientific Information.en
dc.description.provenanceMade available in DSpace on 2019-09-12T16:26:07Z (GMT). No. of bitstreams: 0 Previous issue date: 2007en
dc.languageInglêspt_BR
dc.publisherAsian Network for Scientific Information-
dc.relation.ispartofJournal of Biological Sciences-
dc.rightsAcesso Abertopt_BR
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceScopuspt_BR
dc.subject.otherAngiotensin antagonistsen
dc.subject.otherNitric oxideen
dc.subject.otherReceptorsen
dc.subject.otherSodium metabolismen
dc.subject.otherSupraoptic nucleusen
dc.subject.otherVasopressin antagonist receptoren
dc.subject.other1 (4 dimethylamino 3 methylbenzyl) 5 diphenylacetyl 4,5,6,7 tetrahydro 1h imidazo[4,5 c]pyridine 6 carboxylic aciden
dc.subject.otherangiotensin 1 receptoren
dc.subject.otherangiotensin IIen
dc.subject.otherangiotensin receptor antagonisten
dc.subject.otherarginineen
dc.subject.otherargipressinen
dc.subject.otherargipressin receptoren
dc.subject.otherlosartanen
dc.subject.othern(g) nitroarginine methyl esteren
dc.subject.othernitric oxideen
dc.subject.othersodiumen
dc.subject.othersodium chlorideen
dc.subject.otheranimal experimenten
dc.subject.otheranimal modelen
dc.subject.otheranimal tissueen
dc.subject.otherarticleen
dc.subject.otherbody weighten
dc.subject.othercontrolled studyen
dc.subject.otherhypothalamusen
dc.subject.othernonhumanen
dc.subject.otherprotein interactionen
dc.subject.otherraten
dc.subject.othersodium appetiteen
dc.subject.othersodium intakeen
dc.subject.othersodium metabolismen
dc.subject.otherSprague Dawley raten
dc.subject.othersupraoptic nucleusen
dc.subject.otherRattusen
dc.titleEffects of nitric oxide and arginine vasopressin on sodium intake induced by central angiotensin II. Part 2en
dc.typeArtigo de Periódicopt_BR
dc.description.affiliationSaad, W.A., Basic Institute of Bioscience, University of Taubaté, Taubaté, SP, Brazil, Centro Universitário de Araraquarsa, Araraquara, SP Uniara, Brazil, Department of Physiology and Pathology, School of Dentistry, Paulista State University, Araraquara, SP, Brazil, Department of Gatroenterology, School of Medicine, University of São Paulo, São Paulo, Brazil, Rua Humaitá 1680, 14801-903 Araraquara, SP, Brazil-
dc.description.affiliationGuarda, I.F.M.S., Department of Anesthesiology, Clinic Hospital State of São Paulo, São Paulo, Brazil-
dc.description.affiliationCarmago, L.A. de A., Department of Physiology and Pathology, School of Dentistry, Paulista State University, Araraquara, SP, Brazil-
dc.description.affiliationdos Santos, T.A.F.B., Basic Institute of Bioscience, University of Taubaté, Taubaté, SP, Brazil-
dc.description.affiliationSaad, W.A., Basic Institute of Bioscience, University of Taubaté, Taubaté, SP, Brazil, Centro Universitário de Araraquarsa, Araraquara, SP Uniara, Brazil, Department of Physiology and Pathology, School of Dentistry, Paulista State University, Araraquara, SP, Brazil, Department of Gatroenterology, School of Medicine, University of São Paulo, São Paulo, Brazil, Rua Humaitá 1680, 14801-903 Araraquara, SP, Brazil-
dc.identifier.scopus2-s2.0-34948897022-
dc.contributor.scopus7102555761pt_BR
dc.contributor.scopus6508355383pt_BR
dc.contributor.scopus22233718900pt_BR
dc.contributor.scopus35577775000pt_BR
dc.contributor.scopus7102555761pt_BR
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