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Inhibition of pain behaviour by GABAB receptors in the thalamic ventrobasal complex: effect on normal rats subjected to the formalin test of nociception.

Título
Inhibition of pain behaviour by GABAB receptors in the thalamic ventrobasal complex: effect on normal rats subjected to the formalin test of nociception.
Tipo
Artigo em Revista Científica Internacional
Ano
2006
Autores
Potes C.S.
(Autor)
Outra
A pessoa não pertence à instituição. A pessoa não pertence à instituição. A pessoa não pertence à instituição. Sem AUTHENTICUS Sem ORCID
Neto F.L.
(Autor)
FMUP
Castro-Lopes J.M.
(Autor)
FMUP
Revista
Título: Brain ResearchImportada do Authenticus Pesquisar Publicações da Revista
Vol. 1115 1
Páginas: 37-47
ISSN: 0006-8993
Editora: Elsevier
Classificação Científica
CORDIS: Ciências da Saúde > Neurociências > Neuroquímica
Outras Informações
Abstract (EN): The ventrobasal complex of the thalamus (VB) participates in the transmission and modulation of noxious information. Recent data suggested that GABA(B) receptors in the VB might be involved in the modulation of neuronal activity in response to chronic noxious input. However, in acute inflammatory pain, the role of GABA(B) receptors in the VB remains unknown. The formalin test of nociception was performed in rats stereotaxically injected in the VB contralateral to the formalin-injected paw, with saline (controls), baclofen (0.5 and 0.875 microg), a specific GABA(B) receptor agonist or CGP35348 (25 microg), a GABA(B) receptor antagonist. Control animals exhibited phase 1 (acute pain) and phase 2 (tonic pain) nociception-related activities as previously described. The higher dose of baclofen induced a significant decrease of all pain-related behaviors in both phases of the test and had no observable effects on the animals' motor function, while the lower dose could not reduce the total pain-related activities. Injection of CGP35348 prior to baclofen reduced the antinociceptive effect caused by baclofen during phase 2 in the paw-jerks and in total pain-related activities. CGP35348 alone had antinociceptive effects in both phases, though less pronounced than baclofen 0.875 microg in the total pain-related activities during phase 2. Data demonstrate that both the blockade and the activation of GABA(B) receptors in the VB of rats induce antinociception in acute and tonic pain. An important role for GABA(B) receptors on the thalamic processing of nociceptive input in the VB is suggested.
Idioma: Português
Tipo (Avaliação Docente): Científica
Contacto: fanineto@med.up.pt
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