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dc.contributor.authorCioato, Stefania Giotti-
dc.contributor.authorMedeiros, Liciane Fernandes-
dc.contributor.authorLopes, Bettega Costa-
dc.contributor.authorSouza, Andressa de-
dc.contributor.authorMedeiros, Helouise Richardt-
dc.contributor.authorAssumpção, José Antônio Fagundes-
dc.contributor.authorCaumo, Wolnei-
dc.contributor.authorRoesler, Rafael-
dc.contributor.authorTorres, Iraci L. S.-
dc.date.accessioned2021-08-02T15:39:02Z-
dc.date.available2021-08-02T15:39:02Z-
dc.date.issued2020-
dc.identifier.citationCIOATO, S. G. et al. Antinociceptive and neurochemical effects of a single dose of IB-MECA in chronic pain rat models. Purinergic Signalling, v. 16, n. 4, p. 576-584, dez., 2020. Disponível em: https://link.springer.com/article/10.1007%2Fs11302-020-09751-w. Acesso em: 02 ago. 2021.pt_BR
dc.identifier.urihttp://hdl.handle.net/11690/1907-
dc.description.abstractThis study aimed to evaluate the effect of a single administration of IB-MECA, an A3 adenosine receptor agonist, upon the nociceptive response and central biomarkers of rats submitted to chronic pain models. A total of 136 adult male Wistar rats were divided into two protocols: (1) chronic inflammatory pain (CIP) using complete Freund's adjuvant and (2) neuropathic pain (NP) by chronic constriction injury of the sciatic nerve. Thermal and mechanical hyperalgesia was measured using von Frey (VF), Randal-Selitto (RS), and hot plate (HP) tests. Rats were treated with a single dose of IB-MECA (0.5 μmol/kg i.p.), a vehicle (dimethyl sulfoxide-DMSO), or positive control (morphine, 5 mg/kg i.p.). Interleukin 1β (IL-1β), brain-derived neurotrophic factor (BDNF), and nerve growth factor (NGF) levels were measured in the brainstem and spinal cord using enzyme-linked immunosorbent assay (ELISA). The establishment of the chronic pain (CIP or NP) model was observed 14 days after induction by a decreased nociceptive threshold in all three tests (GEE, P < 0.05). The antinociceptive effect of a single dose of IB-MECA was observed in both chronic pain models, but this was more effective in NP model. There was an increase in IL-1β levels promoted by CIP. NP model promoted increase in the brainstem BDNF levels, which was reversed by IB-MECA.pt_BR
dc.language.isoen_USpt_BR
dc.publisherSpringerpt_BR
dc.rightsOpen Accessen
dc.subjectAdenosine receptorpt_BR
dc.subjectBiomarkerspt_BR
dc.subjectInflammatory painpt_BR
dc.subjectNeuropathic painpt_BR
dc.subjectRatspt_BR
dc.titleAntinociceptive and neurochemical effects of a single dose of IB-MECA in chronic pain rat modelspt_BR
dc.typeArtigopt_BR
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