Diazepam effects on Ehrlich tumor growth and macrophage activity in mice

Autor(es)

Sakai‚ M. ; Fonseca‚ ESM ; Dagli‚ MLZ ; Palermo-Neto‚ J.

• Tipo de documento: Artigo Científico
• Fonte: Life Sciences; v. 78, n. 16, p. 1777-1783, 2006.

Resumo

Besides the central gabaergic receptors described for benzodiazepines, peripheral type binding sites (PBR) were also identified for these molecules in endocrine steroidogenic tissues, immune organs and cells, such as macrophages and lymphocytes. PBR activation was reported to decrease innate immunity and host defense. The present experiment was designed to analyze the effects of diazepam on Ehrlich tumor growth, and on macrophage activity of Ehrlich tumor bearing mice. Results showed that diazepam (3.0 mg/kg/day, for 7 days) increased the number of Ehrlich tumor cells and the volume of tumor-induced ascitic fluid. These effects were not observed after smaller doses of diazepam, suggesting a dose-dependant effect. Furthermore, our results show that 3.0 mg/kg of diazepam, administered daily, for 2 days, decreased (1) the number of peritoneal leukocytes retrieved after injection of the Ehrlich tumor, (2) the percents of macrophage spreading, and (3) the levels of macrophage NO production. Diazepam (3.0 mg/kg/day for 2 days) had no effect on macrophage phagocytosis or on H2O2 production. The present data is discussed based on a direct and/or indirect action of diazepam. Particularly, our findings might be due to a direct effect of diazepam on PBRs present on macrophages and tumor cells, or could still be mediated by PBR stimulation within the hypothalamus-pituitary-adrenal (HPA) axis. (c) 2005 Elsevier Inc. All rights reserved. (AU)

• Processo FAPESP: 02/04975-1 - Efeitos do diazepam sobre a resposta imune de animais portadores do tumor de Ehrlich
• Beneficiário: Mônica Sakai
• Modalidade de apoio: Bolsas no Brasil - Mestrado
• Processo FAPESP: 04/14128-0 - Neuroimunomodulação: efeitos do estresse e de citocinas nas relações bidirecionais entre os sistemas nervosos central e imune
• Beneficiário: João Palermo Neto
• Modalidade de apoio: Auxílio à Pesquisa - Temático