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Novel evidence that nitric oxide of the medial septal area influences the salivary secretion induced by pilocarpine

dc.contributor.authorSaad, W. A.
dc.contributor.authorGuarda, IFMS
dc.contributor.authorCamargo, LAD
dc.contributor.authordos Santos, TAFB
dc.contributor.authorSimoes, S.
dc.contributor.authorGuarda, R. S.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUNITAU
dc.contributor.institutionJulho Med Hosp
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T13:45:45Z
dc.date.available2014-05-20T13:45:45Z
dc.date.issued2002-04-05
dc.description.abstractOur studies have focused on the effect of injection of L-NAME and sodium nitroprussiate (SNP) on the salivary secretion, arterial blood pressure, sodium excretion and urinary volume induced by pilocarpine which was injected into the medial septal area (MSA). Rats were anesthetized with urethane (1.25 g/kg b. wt.) and a stainless steel cannula was implanted into their MSA. The amount of saliva secretion was studied over a five-minute period after injection of pilocarpine into MSA. Injection of pilocarpine (10, 20, 40, 80, 160 mug/mul) into MSA produced a dose-dependent increase in salivary secretion. L-NG-nitro arginine methyl-esther (L-NAME) (40 mug/mul), a nitric oxide (NO) synthase inhibitor, was injected into MSA prior to the injection of pilocarpine into MSA, producing an increase in salivary secretion due to the effect of pilocarpine. Sodium nitroprussiate (SNP) (30 mug/mul) was injected into MSA prior to the injection of pilocarpine into MSA attenuating the increase in salivary secretion induced by pilocarpine. Medial arterial pressure (MAP) increase after injections of pilocarpine into the MSA. L-NAME injected into the MSA prior to injection of pilocarpine into MSA increased the MAP. SNP injected into the MSA prior to pilocarpine attenuated the effect of pilocarpine on MAP. Pilocarpine (40 mug/mul) injected into the MAS induced an increase in sodium and urinary excretion. L-NAME injected prior to pilocarpine into the MSA increased the urinary sodium excretion and urinary volume induced by pilocarpine. SNP injected prior to pilocarpine into the MSA decreased the sodium excretion and urinary volume induced by pilocarpine. All these roles of pilocarpine depend on the release of nitric oxide into the MSA. We may also conclude that the MSA is involved with the cholinergic excitatory mechanism that induce salivary secretion, increase in MAP and increase in sodium excretion and urinary volume. (C) 2002 Elsevier B.V. All rights reserved.en
dc.description.affiliationPaulista State Univ, Dept Physiol & Pathol, Sch Dent, UNESP, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUNITAU, Dept Dent, Taubate, SP, Brazil
dc.description.affiliationJulho Med Hosp, Dept Anesthesiol 9, São Paulo, Brazil
dc.description.affiliationUniv São Paulo, Sch Med, Dept Surg, BR-05508 São Paulo, Brazil
dc.description.affiliationUnespPaulista State Univ, Dept Physiol & Pathol, Sch Dent, UNESP, BR-14801903 Araraquara, SP, Brazil
dc.format.extent2403-2412
dc.identifierhttp://dx.doi.org/10.1016/S0024-3205(02)01531-X
dc.identifier.citationLife Sciences. Oxford: Pergamon-Elsevier B.V., v. 70, n. 20, p. 2403-2412, 2002.
dc.identifier.doi10.1016/S0024-3205(02)01531-X
dc.identifier.issn0024-3205
dc.identifier.urihttp://hdl.handle.net/11449/16123
dc.identifier.wosWOS:000175521500007
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofLife Sciences
dc.relation.ispartofjcr3.234
dc.relation.ispartofsjr1,071
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectpilocarpinept
dc.subjectnitric oxidept
dc.subjectseptal areapt
dc.subjectsalivationpt
dc.subjectarterial pressurept
dc.subjectsodium excretionpt
dc.titleNovel evidence that nitric oxide of the medial septal area influences the salivary secretion induced by pilocarpineen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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