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Interaction of serotonin and cholecystokinin in the lateral parabrachial nucleus to control sodium intake

dc.contributor.authorDe Gobbi, Juliana Irani Fratucci [UNESP]
dc.contributor.authorDe Luca Jr., Laurival Antonio [UNESP]
dc.contributor.authorJohnson, Alan Kim
dc.contributor.authorMenani, José Vanderlei [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversity of Iowa
dc.date.accessioned2022-04-28T19:56:11Z
dc.date.available2022-04-28T19:56:11Z
dc.date.issued2001-01-01
dc.description.abstractInteraction of serotonin and cholecystokinin in the lateral parabrachial nucleus to control sodium intake. Am J Physiol Regulatory Integrative Comp Physiol 280: R1301-R1307, 2001.-Serotonin [5-hydroxytryptamine (5-HT)] and CCK injected into the lateral parabrachial nucleus (LPBN) inhibit NaCl and water intake. In this study, we investigated interactions between 5-HT and CCK into the LPBN to control water and NaCl intake. Male Holtzman rats with cannulas implanted bilaterally in the LPBN were treated with furosemide + captopril to induce water and NaCl intake. Bilateral LPBN injections of high doses of the 5-HT antagonist methysergide (4 μg) or the CCK antagonist proglumide (50 μg), alone or combined, produced similar increases in water and 1.8% NaCl intake. Low doses of methysergide (0.5 μg) + proglumide (20 μg) produced greater increases in NaCl intake than when they were injected alone. The 5-HT2a/2c agonist 2,5-dimetoxy-4-iodoamphetamine hydrobromide (DOI; 5 μg) into the LPBN reduced water and NaCl intake. After proglumide (50 μg) + DOI treatment, the intake was not different from vehicle treatment. CCK-8 (1 μg) alone produced no effect. CCK-8 combined with methysergide (4 μg) reduced the effect of methysergide on NaCl intake. The data suggest that functional interactions between 5-HT and CCK in the LPBN may be important for exerting inhibitory control of NaCl intake.en
dc.description.affiliationDept. of Physiology and Pathology School of Dentistry Paulista State University (UNESP), 14801-903 Araraquara, São Paulo
dc.description.affiliationDepts. of Psychol. and Pharmacol. E. Cardiovascular Center University of Iowa, Iowa City, IA 52242-1407
dc.description.affiliationDept. of Physiology and Pathology School of Dentistry UNESP, Rua Humaitá, 1680, 14801-903 Araraquara-SP
dc.description.affiliationUnespDept. of Physiology and Pathology School of Dentistry Paulista State University (UNESP), 14801-903 Araraquara, São Paulo
dc.description.affiliationUnespDept. of Physiology and Pathology School of Dentistry UNESP, Rua Humaitá, 1680, 14801-903 Araraquara-SP
dc.identifierhttp://dx.doi.org/10.1152/ajpregu.2001.280.5.r1301
dc.identifier.citationAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology, v. 280, n. 5 49-5, 2001.
dc.identifier.doi10.1152/ajpregu.2001.280.5.r1301
dc.identifier.issn0363-6119
dc.identifier.scopus2-s2.0-0343831909
dc.identifier.urihttp://hdl.handle.net/11449/224388
dc.language.isoeng
dc.relation.ispartofAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
dc.sourceScopus
dc.subject5-hydroxytryptamine
dc.subjectAngiotensin II
dc.subjectMethysergide
dc.subjectNaCl intake
dc.subjectProglumide
dc.subjectSodium appetite
dc.titleInteraction of serotonin and cholecystokinin in the lateral parabrachial nucleus to control sodium intakeen
dc.typeArtigopt
dspace.entity.typePublication
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relation.isDepartmentOfPublication.latestForDiscoveryb3ba3d9c-022e-4521-8805-0bcceea7372e
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unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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