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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/67281
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dc.contributor.authorSaad, Wilson Abrão-
dc.contributor.authorDe Arruda Camargo, Luiz Antonio-
dc.date.accessioned2014-05-27T11:20:39Z-
dc.date.accessioned2016-10-25T18:18:37Z-
dc.date.available2014-05-27T11:20:39Z-
dc.date.available2016-10-25T18:18:37Z-
dc.date.issued2003-05-01-
dc.identifierhttp://dx.doi.org/10.1590/S0066-782X2003000400004-
dc.identifier.citationArquivos Brasileiros de Cardiologia, v. 80, n. 4, p. 401-405, 2003.-
dc.identifier.issn0066-782X-
dc.identifier.issn1678-4170-
dc.identifier.urihttp://hdl.handle.net/11449/67281-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/67281-
dc.description.abstractObjective - We determined the effects of losartan and PD 123319 (antagonists of the AT1 and AT2 angiotensin receptors, respectively), and [Sar1, Ala8] ANG II (a relatively peptide antagonist of angiotensin receptors) injected into the paraventricular nucleus (PVN) on water and 3% NaCl intake, and the diuretic, natriuretic, and pressor effects induced by administration of angiotensin II (ANG II) into the medial septal area (MSA) of conscious rats. Methods - Holtzman rats were used. Animals were anesthetized with tribromoethanol (20 mg) per 100 grams of body weight, ip. A stainless steel guide cannula was implanted into the MSA and PVN. All drugs were injected in 0.5-μl volumes for 10-15 seconds. Seven days after brain surgery, water and 3% NaCl intake, urine and sodium excretion, and arterial blood pressure were measured. Results - Losartan (40 nmol) and [Sar1, Ala8] ANG II (40 nmol) completely eliminated whereas PD 123319 (40 nmol) partially blocked the increase in water and sodium intake and the increase in arterial blood pressure induced by ANG II (10 nmol) injected into the MSA. The PVN administration of PD 123319 and [Sar1, Ala8] ANG II blocked whereas losartan attenuated the diuresis and natriuresis induced by MSA administration of ANG II. Conclusion - MSA involvement with PVN on water and sodium homeostasis and arterial pressure modulation utilizing ANGII receptors is suggested.en
dc.format.extent401-405-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBlood pressure-
dc.subjectCentral nervous system-
dc.subjectSodium balance-
dc.subject1 (4 dimethylamino 3 methylbenzyl) 5 diphenylacetyl 4,5,6,7 tetrahydro 1h imidazo[4,5 c]pyridine 6 carboxylic acid-
dc.subjectangiotensin II-
dc.subjectbromethol-
dc.subjectlosartan-
dc.subjectreceptor subtype-
dc.subjectsodium chloride-
dc.subjectstainless steel-
dc.subjectangiotensin receptor-
dc.subjectantihypertensive agent-
dc.subjectimidazole derivative-
dc.subjectpyridine derivative-
dc.subjectsaralasin-
dc.subjectsodium-
dc.subjectvasoconstrictor agent-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectanimal tissue-
dc.subjectarterial pressure-
dc.subjectattenuation-
dc.subjectblood pressure measurement-
dc.subjectbody weight-
dc.subjectbrain surgery-
dc.subjectcannula-
dc.subjectcontrolled study-
dc.subjectdiuresis-
dc.subjectfluid intake-
dc.subjectmale-
dc.subjectmeasurement-
dc.subjectnatriuresis-
dc.subjectnonhuman-
dc.subjectrat-
dc.subjectseptum pellucidum-
dc.subjectsodium excretion-
dc.subjectsodium intake-
dc.subjectthalamus midline nucleus-
dc.subjecturinary excretion-
dc.subjectanimal-
dc.subjectanterior hypothalamus-
dc.subjectblood pressure-
dc.subjectdrinking-
dc.subjectdrug antagonism-
dc.subjectdrug effect-
dc.subjecthomeostasis-
dc.subjectmetabolism-
dc.subjectSprague Dawley rat-
dc.subjectAngiotensin II-
dc.subjectAnimals-
dc.subjectAntihypertensive Agents-
dc.subjectBlood Pressure-
dc.subjectDiuresis-
dc.subjectDrinking-
dc.subjectHomeostasis-
dc.subjectImidazoles-
dc.subjectLosartan-
dc.subjectMale-
dc.subjectParaventricular Hypothalamic Nucleus-
dc.subjectPyridines-
dc.subjectRats-
dc.subjectRats, Sprague-Dawley-
dc.subjectReceptors, Angiotensin-
dc.subjectSaralasin-
dc.subjectSeptum of Brain-
dc.subjectSodium-
dc.subjectVasoconstrictor Agents-
dc.titleInfluence of angiotensin II receptor subtypes of the paraventricular nucleus on the physiological responses induced by angiotensin II injection into the medial septal areaen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Physiology School of Dentistry - Paulista State University UNESP, Rua Humaitá, 1680, 14801-903 - Araraquara, SP-
dc.description.affiliationUnespDepartment of Physiology School of Dentistry - Paulista State University UNESP, Rua Humaitá, 1680, 14801-903 - Araraquara, SP-
dc.identifier.doi10.1590/S0066-782X2003000400004-
dc.identifier.scieloS0066-782X2003000400004-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-4444274375.pdf-
dc.relation.ispartofArquivos Brasileiros de Cardiologia-
dc.identifier.scopus2-s2.0-4444274375-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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