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Glutamate and GABA neurotransmission are increased in paraventricular nucleus of hypothalamus in rats induced to 6-OHDA parkinsonism: Involvement of nNOS

dc.contributor.authorTurossi Amorim, Eric Diego
dc.contributor.authorde Jager, Lorena
dc.contributor.authorMartins, Andressa Busetti
dc.contributor.authorRodrigues, Ananda Totti
dc.contributor.authorCruz Lucchetti, Bruno Fernando
dc.contributor.authorAriza, Deborah
dc.contributor.authorPinge-Filho, Phileno
dc.contributor.authorCrestani, Carlos Cesar [UNESP]
dc.contributor.authorUchoa, Ernane Torres
dc.contributor.authorMartins-Pinge, Marli Cardoso
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2019-10-06T17:04:09Z
dc.date.available2019-10-06T17:04:09Z
dc.date.issued2019-07-01
dc.description.abstractAim: Parkinson's disease (PD) is a progressive neurodegenerative disease that manifests itself clinically after reaching an advanced pathological stage. Besides motor signals, PD patients present cardiovascular and autonomic alterations. Recent data showed that rats induced to Parkinsonism by 6-hydroxydopamine (6-OHDA) administration in the substantia nigra pars compacta (SNpc) showed lower mean arterial pressure (MAP) and heart rate (HR), as reduction in sympathetic modulation. The paraventricular nucleus of the hypothalamus (PVN) is an important site for autonomic and cardiovascular control, and amino acid neurotransmission has a central role. We evaluate PVN amino acid neurotransmission in cardiovascular and autonomic effects of 6-OHDA Parkinsonism. Methods: Male Wistar rats were submitted to guide cannulas implantation into the PVN. 6-OHDA or sterile saline (sham) was administered bilaterally in the SNpc. After 7 days, cardiovascular recordings in conscious state was performed. Results: Bicuculline promoted an increase in MAP and HR in sham group and exacerbated those effects in 6-OHDA group. NBQX (non-NMDA inhibitor) did not promote changes in sham as in 6-OHDA group. On the other hand, PVN microinjection of LY235959 (NMDA inhibitor) in sham group did not induced cardiovascular alterations, but decreased MAP and HR in 6-OHDA group. Compared to Sham group, 6-OHDA lesion increased the number of neuronal nitric oxide synthase (nNOS)-immunoreactive neurons in the PVN and, nNOS inhibition promoted higher increases in MAP and HR. Conclusion: Our data suggest that the decreased baseline blood pressure and heart rate in animals with Parkinsonism may be due to an increased GABAergic tone via nNOS in the PVN.en
dc.description.affiliationDepartament of Physiological Sciences Center of Biological Sciences State University of Londrina
dc.description.affiliationDepartament of Pathological Sciences Center of Biological Sciences State University of Londrina
dc.description.affiliationLaboratory of Pharmacology School of Pharmaceutical Sciences UNESP - Univ Estadual Paulista
dc.description.affiliationUnespLaboratory of Pharmacology School of Pharmaceutical Sciences UNESP - Univ Estadual Paulista
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação Araucária
dc.identifierhttp://dx.doi.org/10.1111/apha.13264
dc.identifier.citationActa Physiologica, v. 226, n. 3, 2019.
dc.identifier.doi10.1111/apha.13264
dc.identifier.issn1748-1716
dc.identifier.issn1748-1708
dc.identifier.scopus2-s2.0-85062319987
dc.identifier.urihttp://hdl.handle.net/11449/190155
dc.language.isoeng
dc.relation.ispartofActa Physiologica
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectarterial pressure
dc.subjectbaroreflex
dc.subjectbicuculline
dc.subjectheart rate
dc.subjectheart rate variability
dc.subjectnitric oxide
dc.titleGlutamate and GABA neurotransmission are increased in paraventricular nucleus of hypothalamus in rats induced to 6-OHDA parkinsonism: Involvement of nNOSen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes1117432571971568[8]
unesp.author.orcid0000-0002-9444-1530[10]
unesp.author.orcid0000-0002-1942-858X[8]
unesp.departmentPrincípios Ativos Naturais e Toxicologia - FCFpt

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