CIBICI   14215
CENTRO DE INVESTIGACION EN BIOQUIMICA CLINICA E INMUNOLOGIA
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Diazepam inhibits acute innate and ongoing adaptive inflammatory responses
Autor/es:
C R FALCON; MONFERRAN C; . CERVI L.; ROTH G
Lugar:
Mar del Plata
Reunión:
Congreso; LXII Reunión anual. Sociedad Argentina de Inmunología; 2014
Institución organizadora:
Sociedad Argentina de Inmunología
Resumen:
663. (721) DIAZEPAM INHIBITS ACUTE INNATE AND ONGOING ADAPTIVE INFLAMMATORY RESPONSES Falcón, Cristian Roberto1; Monferrán Clara G. 1; Cervi Laura2; Roth Germán A. 1. Centro de Investigaciones en Química Biológica de Córdoba1- Centro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-CONICET-UNC2 In addition to the central GABAergic receptors described for benzodiazepines, peripheral-type benzodiazepine receptor (PBR) was also identifid for these molecules in immune cells, such as macrophages and lymphocytes. PBR activation was reported to decrease inflmmatory immune responses. In this regard, we previously demonstrated that Diazepam (Dz) decreases LPS-induced dendritic cell activation and their ability to induce allogeneic responses, thus preventing the initiation of immune responses. In this work we demonstrate that Dz is able to diminish acute innate and adaptive ongoing inflmmatory responses in vivo. For this, we treated C57BL/6 mice with Dz (2mg/Kg) at days 0, 2 and 4, and 12 h after the last treatment the mice were injected (i.p.) with 800 µg de LPS. Dz was able to prevent LPS-induced death and inhibit the IL-6 secretion (p