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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/64858
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dc.contributor.authorDe Luca Jr., Laurival A.-
dc.contributor.authorBarbosa, Silas P.-
dc.contributor.authorSugawara, Alexandre M.-
dc.contributor.authorMenani, José Vanderlei-
dc.date.accessioned2014-05-27T11:18:07Z-
dc.date.accessioned2016-10-25T18:14:00Z-
dc.date.available2014-05-27T11:18:07Z-
dc.date.available2016-10-25T18:14:00Z-
dc.date.issued1996-10-08-
dc.identifierhttp://dx.doi.org/10.1016/S0167-0115(96)00055-9-
dc.identifier.citationRegulatory Peptides, v. 66, n. 1-2, p. 31-35, 1996.-
dc.identifier.issn0167-0115-
dc.identifier.urihttp://hdl.handle.net/11449/64858-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/64858-
dc.description.abstractAngiotensin II (Ang II) non-peptide antagonists were injected i.c.v. (6.25-200 nmol, n = 5-8 rats/group): In sodium replete rats, losartan (AT1 receptor antagonist) induced an increase in mean arterial pressure (MAP) and in heart rate (HR) by 3rd ventricular (3rdV) injection, and a weaker pressor response and bradycardia by 4th ventricular (4thV) injection. PD123319 (AT2 receptor antagonist) induced an increase in MAP and in HR by 3rdV injection, and an increase in MAP and no alteration in HR by 4thV injection. In sodium deplete (furosemide plus removal of ambient sodium for 24 h) rats, losartan induced an increase in MAP and no alteration in HR by 3rdV injection, and no alteration in MAP and bradycardia by 4thV injection. PD123319 induced an increase in MAP and in HR by 3rdV injection, and an increase in MAP and bradycardia by 4thV injection. Thus, there was no fall in MAP by central injections of Ang II antagonists. Intravenous injection of losartan, but not of PD123319, induced a fall in MAP in both sodium replete and sodium deplete animals. Therefore, losartan and PD123319 can have similar effects on MAP and HR when injected intracerebroventricularly, although some differences are also present. The bradycardia is consistent with an withdrawal of Ang II inhibitory action on baroreflex.en
dc.format.extent31-35-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAngiotensin II-
dc.subjectAngiotensin receptor subtype-
dc.subjectAT1 receptor-
dc.subjectAT2 receptor-
dc.subjectSodium depletion-
dc.subject1 (4 dimethylamino 3 methylbenzyl) 5 diphenylacetyl 4,5,6,7 tetrahydro 1h imidazo[4,5 c]pyridine 6 carboxylic acid-
dc.subjectangiotensin 1 receptor-
dc.subjectangiotensin 2 receptor-
dc.subjectangiotensin 2 receptor antagonist-
dc.subjectfurosemide-
dc.subjectlosartan-
dc.subjectanimal experiment-
dc.subjectarterial pressure-
dc.subjectcontrolled study-
dc.subjectheart rate-
dc.subjectintracerebroventricular drug administration-
dc.subjectmale-
dc.subjectnonhuman-
dc.subjectpressoreceptor-
dc.subjectpriority journal-
dc.subjectrat-
dc.subjectsodium depletion-
dc.subjectAnimals-
dc.subjectBiphenyl Compounds-
dc.subjectBlood Pressure-
dc.subjectCohort Studies-
dc.subjectHeart Rate-
dc.subjectImidazoles-
dc.subjectInjections, Intraventricular-
dc.subjectLosartan-
dc.subjectMale-
dc.subjectPyridines-
dc.subjectRats-
dc.subjectReceptors, Angiotensin-
dc.subjectSodium-
dc.subjectTetrazoles-
dc.subjectAnimalia-
dc.subjectTheilovirus-
dc.titleEffects of intracerebroventricular injections of losartan or PD123319 on arterial pressure and heart rate of sodium replete and sodium deplete ratsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Physiological Sciences School of Odontology Paulista State University (UNESP), 14801-906 Araraquara, Sao Paulo-
dc.description.affiliationUnespDepartment of Physiological Sciences School of Odontology Paulista State University (UNESP), 14801-906 Araraquara, Sao Paulo-
dc.identifier.doi10.1016/S0167-0115(96)00055-9-
dc.identifier.wosWOS:A1996VN31600006-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofRegulatory Peptides-
dc.identifier.scopus2-s2.0-0030575633-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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