Central moxonidine on water and NaCl intake
dc.contributor.author | Menani, José Vanderlei [UNESP] | |
dc.contributor.author | Sato, M. A. | |
dc.contributor.author | Haikel, L. | |
dc.contributor.author | Vieira, A. A. | |
dc.contributor.author | de Andrade, CAF | |
dc.contributor.author | da Silva, DCF | |
dc.contributor.author | Renzi, Antonio [UNESP] | |
dc.contributor.author | De Luca, L. A. | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-05-20T15:29:13Z | |
dc.date.available | 2014-05-20T15:29:13Z | |
dc.date.issued | 1999-07-01 | |
dc.description.abstract | In 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.affiliation | UNESP, Fac Odontol, Dept Ciências Fisiol, BR-14801903 Araraquara, SP, Brazil | |
dc.description.affiliationUnesp | UNESP, Fac Odontol, Dept Ciências Fisiol, BR-14801903 Araraquara, SP, Brazil | |
dc.format.extent | 273-279 | |
dc.identifier | http://dx.doi.org/10.1016/S0361-9230(99)00059-3 | |
dc.identifier.citation | Brain Research Bulletin. Oxford: Pergamon-Elsevier B.V., v. 49, n. 4, p. 273-279, 1999. | |
dc.identifier.doi | 10.1016/S0361-9230(99)00059-3 | |
dc.identifier.issn | 0361-9230 | |
dc.identifier.lattes | 1023597870118105 | |
dc.identifier.lattes | 6551236936295697 | |
dc.identifier.uri | http://hdl.handle.net/11449/38848 | |
dc.identifier.wos | WOS:000081399800005 | |
dc.language.iso | eng | |
dc.publisher | Elsevier B.V. | |
dc.relation.ispartof | Brain Research Bulletin | |
dc.relation.ispartofjcr | 3.440 | |
dc.relation.ispartofsjr | 1,398 | |
dc.rights.accessRights | Acesso restrito | pt |
dc.source | Web of Science | |
dc.subject | salt appetite | pt |
dc.subject | thirst | pt |
dc.subject | angiotensin | pt |
dc.subject | water deprivation | pt |
dc.subject | alpha(2) adrenergic receptors | pt |
dc.subject | imidazoline receptors | pt |
dc.title | Central moxonidine on water and NaCl intake | en |
dc.type | Artigo | pt |
dcterms.license | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dcterms.rightsHolder | Elsevier B.V. | |
dspace.entity.type | Publication | |
relation.isDepartmentOfPublication | b3ba3d9c-022e-4521-8805-0bcceea7372e | |
relation.isDepartmentOfPublication.latestForDiscovery | b3ba3d9c-022e-4521-8805-0bcceea7372e | |
relation.isOrgUnitOfPublication | ca4c0298-cd82-48ee-a9c8-c97704bac2b0 | |
relation.isOrgUnitOfPublication.latestForDiscovery | ca4c0298-cd82-48ee-a9c8-c97704bac2b0 | |
unesp.author.lattes | 1023597870118105 | |
unesp.author.lattes | 6551236936295697 | |
unesp.author.lattes | 9055280555067656[5] | |
unesp.author.orcid | 0000-0001-8270-2652[8] | |
unesp.author.orcid | 0000-0003-1167-4441[1] | |
unesp.author.orcid | 0000-0003-3393-2202[5] | |
unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquara | pt |
unesp.department | Fisiologia e Patologia - FOAR | pt |
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