Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Neurol Res ; 31(4): 432-8, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19243685

RESUMO

OBJECTIVE: It is still not known whether the glial cell activation of locus coeruleus (LC) is involved in the neurophysiologic mechanism of the acute phase of heart disease. The aim of this study was to investigate whether the glial cell activation of LC responds to acute cardiac injury (ACI). METHODS: In this study, ACI was established by intramyocardial injection of formalin. Afterward, we analysed c-Fos, OX42, GFAP and P2X(4)R expression levels in the LC of the rats by immunofluorescence staining or Western blot analysis. RESULTS: There was no significant difference in the levels of these markers in the LC between the normal control and the sham-operated groups. Following ACI, up-regulation of GFAP, OX42 and P2X(4)R expression levels were observed in locus coeruleus of the rats. The peak expression time was at hour 24. P2X(4)R was colocalized with OX42 in activated microglias, but not with GFAP in activated astrocytes. Compared with the control group, the ACI group showed a high expression level of c-Fos at hour 1 with a peak expression level at hour 2. CONCLUSION: The results showed that LC glia cells, like neurons, could sensitively respond to cardiovascular nociception induced by ACI at different time points. Results of this study may provide insights into the role of glial activation in response to ACI and may represent a potential strategy for investigation of neurophysiologic mechanism of cardiac pain.


Assuntos
Astrócitos/metabolismo , Cardiopatias/complicações , Locus Cerúleo/patologia , Microglia/metabolismo , Dor/etiologia , Dor/patologia , Doença Aguda , Animais , Antígeno CD11b/metabolismo , Modelos Animais de Doenças , Formaldeído , Proteína Glial Fibrilar Ácida/metabolismo , Cardiopatias/induzido quimicamente , Masculino , Proteínas Proto-Oncogênicas c-fos/metabolismo , Ratos , Ratos Endogâmicos WKY , Receptores Purinérgicos P2/metabolismo , Receptores Purinérgicos P2X4 , Fatores de Tempo , Regulação para Cima/efeitos dos fármacos , Regulação para Cima/fisiologia
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa