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dc.contributor.authorSaad, W. A.
dc.contributor.authorCamargo, LAD
dc.contributor.authorSimoes, S.
dc.contributor.authorGuarda, R. S.
dc.contributor.authorGuarda, IFMS
dc.date.accessioned2014-05-20T13:45:44Z
dc.date.available2014-05-20T13:45:44Z
dc.date.issued2004-05-31
dc.identifierhttp://dx.doi.org/10.1016/j.autneu.2004.04.001
dc.identifier.citationAutonomic Neuroscience-basic & Clinical. Amsterdam: Elsevier B.V., v. 112, n. 1-2, p. 31-36, 2004.
dc.identifier.issn1566-0702
dc.identifier.urihttp://hdl.handle.net/11449/16110
dc.description.abstractWe determined the effects of moxonidine and rilmenidine 20 mol (alpha(2)-adrenergic and imidazoline receptor agonists) injected into the medial septal area (MSA) on the pilocarpine-induced salivation, when injected intraperitoneally (i.p.), of male Holtzman rats weighing 250300 g, with stainless-steel cannula implanted into the MSA. The rats were anesthetized with zoletil 50 mg kg(-1) b.wt. (tiletamine chloridrate 125.0 mg and zolazepan chloridrate 125.0 mg) into quadriceps muscle intramuscularly (IM), saliva was collected using pre-weighed small cotton balls inserted in the animal's mouth. The pre-treatment with moxonidine injected into the MSA reduced the salivation induced by pilocarpine (1 mg kg(-1)) injected i.p. (12 +/- 3 mg min(-1)) vs. control (99 +/- 9 mg min(-1)). The pre-treatment with rilmenidine 40 nmol also reduced the salivation induce by pilocarpine injected i.p. (20 +/- 5 mg min(-1)) vs. control (94 +/- 7 mg min(-1)). Idazoxan 40 nmol (imidazoline receptor antagonist) injected into the MSA previous to moxonidine and rilmenidine partially blocked the effect of moxonidine and totally blocked the rilmenidine effect in pilocarpine-induced salivation injected i.p. (60 +/- 8 and 95 +/- 10 mg min(-1), respectively). Yohimbine 40 nmol (alpha(2)-adrenergic receptor antagonist) injected into the MSA previously to moxonidine and rilmenidine partially blocked the moxonidine effect but produced no change on the rilmenidine effect on i.p. pilocarpine-induced salivation (70 +/- 6 and 24 +/- 6 mg min(-1), respectively). Injection of these alpha(2)-adrenergic and imidazoline agonists and antagonists agents i.p. produced no change on i.p. pilocarpine-induced salivation. These results show that central, but not peripheral, injection of alpha(2)-adrenergic and imidazoline agonists' agents inhibit pilocarpine-induced salivation. Idazoxan, an imidazoline receptor antagonist, totally inhibits the rilmenidine effect and partially inhibits the moxonidine effect on pilocarpine-induced salivation. Yohimbine produced no change on rilmenidine effect but partially inhibited the moxonidine effect. Both of these antagonists when injected into the MSA previous to pilocarpine i.p. potentiated the sialogogue effect of pilocarpine. The results suggest that alpha(2)-adrenergic/imidazoline receptor of the MSA when stimulated blocked pilocarpine-induced salivation in rats when injected intraperitonially These receptors of the medial septal area have an inhibitory mechanism on salivary secretion. (C) 2004 Elsevier B.V. All rights reserved.en
dc.format.extent31-36
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofAutonomic Neuroscience-basic & Clinical
dc.sourceWeb of Science
dc.subjectparasympatheticpt
dc.subjectrilmenidinept
dc.subjectmoxonidinept
dc.subjectadrenergic/imidazoline receptorspt
dc.subjectseptal areapt
dc.titleMoxonidine and rilmenidine injected into the medial septal area reduces the salivation induced by pilocarpineen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniv Taubate
dc.contributor.institutionUNIARA
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.description.affiliationUNESP, Paulista State Univ, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUniv Taubate, UNITAU, Dept Odontol, Taubate, SP, Brazil
dc.description.affiliationUNIARA, Dept Nat Sci, Araraquara, SP, Brazil
dc.description.affiliationUniv Fed Sao Carlos, Dept Physiol Sci, Sao Carlos, SP, Brazil
dc.description.affiliationUnespUNESP, Paulista State Univ, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, Brazil
dc.identifier.doi10.1016/j.autneu.2004.04.001
dc.identifier.wosWOS:000222896400004
dc.rights.accessRightsAcesso restrito
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Odontologia, Araraquarapt
dc.relation.ispartofjcr2.605
dc.relation.ispartofsjr0,902
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