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Effects of acetylcholine and cholinergic antagonists on the activity of nucleus of the solitary tract neurons

dc.contributor.authorFuruya, Werner I. [UNESP]
dc.contributor.authorColombari, Eduardo [UNESP]
dc.contributor.authorFerguson, Alastair V.
dc.contributor.authorColombari, Debora S. A. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionQueens Univ
dc.date.accessioned2018-11-26T17:20:52Z
dc.date.available2018-11-26T17:20:52Z
dc.date.issued2017-03-15
dc.description.abstractPreviously we have demonstrated that microinjection of acetylcholine (ACh) into the intermediate nucleus of the solitary tract (iNTS) induced sympatho-inhibition combined with a decrease in the phrenic nerve activity (PNA), whereas in the commissural NTS (cNTS), ACh did not change sympathetic nerve activity (SNA), but increased the PNA. In view of these demonstrated distinctive effects of ACh in different subnuclei of the NTS the current studies were undertaken to examine, using patch clamp techniques, the specific effects of ACh on the excitability of individual neurons in the NTS, as well as the neuropharmacology of these actions. Coronal slices of the brainstem containing either cNTS or iNTS subnuclei were used, and whole cell patch clamp recordings obtained from individual neurons in these two subnuclei. In cNTS, 58% of recorded neurons (n = 12) demonstrated rapid reversible depolarizations in response to ACh (10 mM), effects which were inhibited by the nicotinic antagonist mecamylamine (10 mu M), but unaffected by the muscarinic antagonist atropine (10 mu M). Similarly, bath application of ACh depolarized 76% of iNTS neurons (n = 17), although in this case both atropine and mecamylamine reduced the ACh-induced depolarization. These data demonstrate that ACh depolarizes cNTS neurons through actions on nicotinic receptors, while depolarizing effects in iNTS are apparently mediated by both receptors. (C) 2017 Elsevier B.V. All rights reserved.en
dc.description.affiliationSao Paulo State Univ, Sch Dent, Dept Physiol & Pathol, Araraquara, SP, Brazil
dc.description.affiliationQueens Univ, Sch Med, Dept Biomed & Mol Sci, Kingston, ON, Canada
dc.description.affiliationUnespSao Paulo State Univ, Sch Dent, Dept Physiol & Pathol, Araraquara, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipCanadian Institutes of Health Research
dc.description.sponsorshipIdFAPESP: FAPESP 2011/20040-1
dc.description.sponsorshipIdFAPESP: 2010/17218-0
dc.description.sponsorshipIdFAPESP: 2009/54888-7
dc.description.sponsorshipIdFAPESP: 2012/05844-0
dc.description.sponsorshipIdCanadian Institutes of Health Research: MOP12192
dc.format.extent136-141
dc.identifierhttp://dx.doi.org/10.1016/j.brainres.2017.01.027
dc.identifier.citationBrain Research. Amsterdam: Elsevier Science Bv, v. 1659, p. 136-141, 2017.
dc.identifier.doi10.1016/j.brainres.2017.01.027
dc.identifier.fileWOS000395600000014.pdf
dc.identifier.issn0006-8993
dc.identifier.urihttp://hdl.handle.net/11449/162542
dc.identifier.wosWOS:000395600000014
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofBrain Research
dc.relation.ispartofsjr1,404
dc.rights.accessRightsAcesso abertopt
dc.sourceWeb of Science
dc.subjectNicotinic receptors
dc.subjectMuscarinic receptors
dc.subjectAcetylcholine
dc.subjectPatch clamp
dc.titleEffects of acetylcholine and cholinergic antagonists on the activity of nucleus of the solitary tract neuronsen
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.lattes4544450092427426[2]
unesp.author.orcid0000-0002-1395-4036[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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