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Central moxonidine on water and NaCl intake

dc.contributor.authorMenani, José Vanderlei [UNESP]
dc.contributor.authorSato, M. A.
dc.contributor.authorHaikel, L.
dc.contributor.authorVieira, A. A.
dc.contributor.authorde Andrade, CAF
dc.contributor.authorda Silva, DCF
dc.contributor.authorRenzi, Antonio [UNESP]
dc.contributor.authorDe Luca, L. A.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:29:13Z
dc.date.available2014-05-20T15:29:13Z
dc.date.issued1999-07-01
dc.description.abstractIn this study we investigated: (a) the effects of intracerebroventricular (i.c.v.) injections of moxonidine (an alpha(2)-adrenergic and imidazoline receptor agonist) on the ingestion of water and NaCl induced by 24 h of water deprivation; (b) the effects of i.c.v. injection of moxonidine on central angiotensin II (ANG II)- and carbachol-induced water intake; (c) the effects of the pre-treatment with i.c.v, idazoxan (an alpha(2)-adrenergic and imidazoline receptor antagonist) and RX 821002 (a selective alpha(2)-adrenergic antagonist) on the antidipsogenic action of central moxonidine. Male Holtzman rats had stainless steel cannulas implanted in the lateral cerebral ventricle. Intracerebroventricular injection of moxonidine (5 and 20 nmol/1 mu l) reduced the ingestion of 1.5% NaCl solution (4.1 +/- 1.1 and 2.9 +/- 2.5 ml/2 h, respectively vs. control = 7.4 +/- 2.1 ml/2 h) and water intake (2.0 +/- 0.6 and 0.3 +/- 0.2 ml/h, respectively vs. control = 13.0 +/- 1.4 ml/h) induced by water deprivation, Intracerebroventricular moxonidine (5 nmol/1 mu l) also reduced i.c.v. ANG Ii-induced water intake (2.8 +/- 0.9 vs. control = 7.9 +/- 1.7 ml/1 h) and i.c.v. moxonidine (10 and 20 nmol/1 mu l) reduced i.c.v. carbachol-induced water intake (4.3 +/- 1.7 and 2.1 +/- 0.9, respectively vs. control = 9.2 +/- 1.0 ml/1 h). The pre-treatment with i.c.v. idazoxan (40 to 320 nmol/1 mu l) abolished the inhibitory effect of i.c.v, moxonidine on carbachol-induced water intake. Intracerebroventricular idazoxan (320 nmol/1 mu l) partially reduced the inhibitory effect of moxonidine on water deprivation-induced water intake and produced only a tendency to reduce the antidipsogenic effect of moxonidine on ANG Ii-induced water intake. RX 821002 (80 and 160 nmol/1 mu l) completely abolished the antidipsogenic action of moxonidine on ANG Ii-induced water intake. The results show that central injections c: moxonidine strongly inhibit water and NaCl ingestion. They also suggest the involvement of central alpha(2)-adrenergic receptors in the antidipsogenic action of moxonidine. (C) 1999 Elsevier B.V.en
dc.description.affiliationUNESP, Fac Odontol, Dept Ciências Fisiol, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Odontol, Dept Ciências Fisiol, BR-14801903 Araraquara, SP, Brazil
dc.format.extent273-279
dc.identifierhttp://dx.doi.org/10.1016/S0361-9230(99)00059-3
dc.identifier.citationBrain Research Bulletin. Oxford: Pergamon-Elsevier B.V., v. 49, n. 4, p. 273-279, 1999.
dc.identifier.doi10.1016/S0361-9230(99)00059-3
dc.identifier.issn0361-9230
dc.identifier.lattes1023597870118105
dc.identifier.lattes6551236936295697
dc.identifier.urihttp://hdl.handle.net/11449/38848
dc.identifier.wosWOS:000081399800005
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofBrain Research Bulletin
dc.relation.ispartofjcr3.440
dc.relation.ispartofsjr1,398
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectsalt appetitept
dc.subjectthirstpt
dc.subjectangiotensinpt
dc.subjectwater deprivationpt
dc.subjectalpha(2) adrenergic receptorspt
dc.subjectimidazoline receptorspt
dc.titleCentral moxonidine on water and NaCl intakeen
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.author.lattes1023597870118105
unesp.author.lattes6551236936295697
unesp.author.lattes9055280555067656[5]
unesp.author.orcid0000-0001-8270-2652[8]
unesp.author.orcid0000-0003-1167-4441[1]
unesp.author.orcid0000-0003-3393-2202[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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