Logotipo do repositório
 

Publicação:
Inhibitory mechanism of the nucleus of the solitary tract involved in the control of cardiovascular, dipsogenic, hormonal, and renal responses to hyperosmolality

dc.contributor.authorBlanch, Graziela T. [UNESP]
dc.contributor.authorFreiria-Oliveira, André H. [UNESP]
dc.contributor.authorMurphy, David
dc.contributor.authorPaulin, Renata F.
dc.contributor.authorAntunes-Rodrigues, José
dc.contributor.authorColombari, Eduardo [UNESP]
dc.contributor.authorMenani, José Vanderlei [UNESP]
dc.contributor.authorColombari, Débora S.A. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Bristol
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-27T11:29:40Z
dc.date.available2014-05-27T11:29:40Z
dc.date.issued2013-06-11
dc.description.abstractThe nucleus of the solitary tract (NTS) is the primary site of visceral afferents to the central nervous system. In the present study, we investigated the effects of lesions in the commissural portion of the NTS (commNTS) on the activity of vasopressinergic neurons in the hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei, plasma vasopressin, arterial pressure, water intake, and sodium excretion in rats with plasma hyperosmolality produced by intragastric 2 M NaCl (2 ml/rat). Male Holtzman rats with 15-20 days of sham or electrolytic lesion (1 mA; 10 s) of the commNTS were used. CommNTS lesions enhanced a 2 M NaCl intragastrically induced increase in the number of vasopressinergic neurons expressing c-Fos in the PVN (28 ± 1, vs. sham: 22 ± 2 c-Fos/AVP cells) and SON (26 ± 4, vs. sham: 11 ± 1 c-Fos/AVP cells), plasma vasopressin levels (21 ± 8, vs. sham: 6.6 ± 1.3 pg/ml), pressor responses (25 ± 7 mmHg, vs. sham: 7 ± 2 mmHg), water intake (17.5 ± 0.8, vs. sham: 11.2 ± 1.8 ml/2 h), and natriuresis (4.9 ± 0.8, vs. sham: 1.4 ± 0.3 meq/1 h). The pretreatment with vasopressin antagonist abolished the pressor response to intragastric 2 M NaCl in commNTS-lesioned rats (8 ± 2.4 mmHg at 10 min), suggesting that this response is dependent on vasopressin secretion. The results suggest that inhibitory mechanisms dependent on commNTS act to limit or counterbalance behavioral, hormonal, cardiovascular, and renal responses to an acute increase in plasma osmolality. © 2013 the American Physiological Society.en
dc.description.affiliationDepartment of Physiology and Pathology School of Dentistry São Paulo State University, Araraquara, SP
dc.description.affiliationHenry Wellcome Laboratories for Integrative Neuroscience University of Bristol
dc.description.affiliationDepartment of Physiology School of Medicine of Ribeirão Preto University of São Paulo, Ribeirão Preto, SP
dc.description.affiliationUnespDepartment of Physiology and Pathology School of Dentistry São Paulo State University, Araraquara, SP
dc.identifierhttp://dx.doi.org/10.1152/ajpregu.00191.2012
dc.identifier.citationAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology, v. 304, n. 7, 2013.
dc.identifier.doi10.1152/ajpregu.00191.2012
dc.identifier.issn0363-6119
dc.identifier.issn1522-1490
dc.identifier.lattes4544450092427426
dc.identifier.lattes1023597870118105
dc.identifier.scopus2-s2.0-84878258048
dc.identifier.urihttp://hdl.handle.net/11449/75631
dc.identifier.wosWOS:000317001600006
dc.language.isoeng
dc.relation.ispartofAmerican Journal of Physiology: Regulatory Integrative and Comparative Physiology
dc.relation.ispartofjcr3.082
dc.relation.ispartofsjr1,550
dc.relation.ispartofsjr1,550
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.subjectBlood pressure
dc.subjectC-Fos expression
dc.subjectOsmoreceptor
dc.subjectThirst
dc.subjectVasopressin
dc.subjectsodium chloride
dc.subjectvasopressin
dc.subjectvasopressin antagonist
dc.subjectoxytocin
dc.subjectprotein c fos
dc.subjectvasopressin derivative
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectarterial pressure
dc.subjectbrain stem injury
dc.subjectcardiovascular function
dc.subjectheart rate
dc.subjecthormone action
dc.subjecthormone blood level
dc.subjecthyperosmolality
dc.subjecthypothalamic paraventricular nucleus
dc.subjectkidney function
dc.subjectmale
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectrat
dc.subjectsolitary tract nucleus
dc.subjectsolitary tract nucleus lesion
dc.subjectthirst
dc.subjectanimal
dc.subjectblood pressure
dc.subjectcytology
dc.subjectdrinking
dc.subjectgenetics
dc.subjectkidney
dc.subjectmetabolic disorder
dc.subjectmetabolism
dc.subjectosmolarity
dc.subjectphysiology
dc.subjectSprague Dawley rat
dc.subjectsupraoptic nucleus
dc.subjectAnimals
dc.subjectBlood Pressure
dc.subjectDrinking
dc.subjectKidney
dc.subjectMale
dc.subjectOsmolar Concentration
dc.subjectOxytocin
dc.subjectParaventricular Hypothalamic Nucleus
dc.subjectProto-Oncogene Proteins c-fos
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectSolitary Nucleus
dc.subjectSupraoptic Nucleus
dc.subjectVasopressins
dc.subjectWater-Electrolyte Imbalance
dc.titleInhibitory mechanism of the nucleus of the solitary tract involved in the control of cardiovascular, dipsogenic, hormonal, and renal responses to hyperosmolalityen
dc.typeArtigopt
dcterms.licensehttp://www.the-aps.org/mm/Publications/Info-For-Authors/Copyright
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[6]
unesp.author.lattes1023597870118105
unesp.author.orcid0000-0002-1395-4036[6]
unesp.author.orcid0000-0003-1167-4441[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

Arquivos