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dc.contributor.authorSaad, Wilson Abraopt_BR
dc.contributor.authorGuarda, Ismael Francisco Mota Siqueirapt_BR
dc.contributor.authorCamargo, Luiz Antonio de Arrudapt_BR
dc.contributor.authorFaria Brizola dos Santos, TApt_BR
dc.contributor.authorSaad, Wilson Abraopt_BR
dc.date.accessioned2019-09-12T16:53:40Z-
dc.date.available2019-09-12T16:53:40Z-
dc.date.issued2006-
dc.citation.volume83pt_BR
dc.citation.issue4pt_BR
dc.citation.spage598-
dc.citation.epage602-
dc.identifier.doi10.1016/j.pbb.2006.03.023pt_BR
dc.identifier.issn0091-3057-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/2701-
dc.description.abstractCalcium ions are widely accepted as critically important in responses of neurons to a stimulus. We have show previously the central involvement of angiotensin II (ANGII) in water intake. This study determined whether voltage-dependent calcium channels are involved in ANGII-induced behavioral drinking implicating nitrergic mechanism. The antidipsogenic actions of L-type calcium channel antagonists nifedipine, on ANGII-induced drinking behavior were studied when it is injected into the median preoptic nucleus (MnPO). The influence of nitric oxide (NO) on nifedipine antidipsogenic action was also studied by utilizing the N-W-nitro-L-arginine methyl ester (L-NAME) a constitutive nitric oxide synthase inhibitor constitutive (cNOSI) and 7-nitroindazol (7-NIT) a specific neuronal nitric oxide synthase inhibitor (nNOSI) and L-arginine a NO donor. Rats 200-250 g, with cannulae implanted into MnPO, pre-treated into MnPO with either nifedipine, followed by ANGII, drank significantly less water than controls during the first 15 min after injection. However, L-NAME potentiated the dipsogenic effect of ANGII that is blocked by prior injection of nifedipine and L-arginine. 7-NIT injected prior to ANGII into MnPO also potentiated the dipsogenic effect of ANGII but with a less intensity than L-NAME that it is also blocked by prior injection of nifedipine. The results described in this paper provide evidence that calcium channels play important roles in the ANGII-induced behavioral water intake. The structures containing NO in the brain such as MnPO include both endothelial cells and neurons might be responsible for the influence of nifedipine on dipsogenic effect of ANGII. These data shows the correlation between L-type calcium channel and a free radical gas NO produced endogenously from amino acids L-arginine by endothelial and neuronal NO synthase in the control of ANGII-dipsogenic effect. This suggests that an L-type calcium channel participates in both short- and longer-term neuronal actions of ANGII by nitrergic way. (c) 2006 Elsevier Inc. All rights reserved.en
dc.description.provenanceMade available in DSpace on 2019-09-12T16:53:40Z (GMT). No. of bitstreams: 0 Previous issue date: 2006en
dc.languageInglêspt_BR
dc.publisherPergamon-Elsevier Science Ltd-
dc.publisher.countryInglaterrapt_BR
dc.relation.ispartofPharmacology Biochemistry and Behavior-
dc.rightsEm verificaçãopt_BR
dc.sourceWeb of Sciencept_BR
dc.subject.otherAngiotensin Iien
dc.subject.otherCalcium Channelen
dc.subject.otherNitric Oxide Drinking Behavioren
dc.subject.otherMnpoen
dc.subject.otherC-Fos Expressionen
dc.subject.otherIntraventricular Infusionsen
dc.subject.otherDrinking Behavioren
dc.subject.otherModulationen
dc.subject.otherResponsesen
dc.subject.otherBrainen
dc.subject.otherReceptorsen
dc.subject.otherSodiumen
dc.subject.otherSitesen
dc.titleL-Type calcium channels mediate water intake induced by angiotensin injection into median preoptic nucleusen
dc.typeArtigo de Periódicopt_BR
dc.identifier.wosWOS:000238497300016-
dc.description.affiliationUniv Estadual Paulista, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, Brazil; , Basic Inst Biosci; UNIARA, Dept Exact & Nat Sci, Araraquara, SP, Brazil; Clin Hosp State Sao Paulo, Dept Anesthesiol, Sao Paulo, Brazil; Univ Fed Sao Carlos, Dept Physiol, BR-13560 Sao Carlos, SP, Brazil; Univ Sao Paulo, Clin Hosp, Dept Gastroenterol, Sao Paulo, Brazil-
dc.subject.wosareaBehavioral Sciencesen
dc.subject.wosareaNeurosciencesen
dc.subject.wosareaPharmacology & Pharmacyen
dc.subject.researchareaBehavioral Sciencesen
dc.subject.researchareaNeurosciences & Neurologyen
dc.subject.researchareaPharmacology & Pharmacyen
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