Sakai M, Fonseca E S M, Dagli M L Z, Palermo-Neto J
Applied Pharmacology and Toxicology Laboratory, School of Veterinary Medicine, University of São Paulo, São Paulo, SP, Brazil.
Life Sci. 2006 Mar 13;78(16):1777-83. doi: 10.1016/j.lfs.2005.08.015. Epub 2005 Oct 28.
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.
除了已描述的苯二氮䓬类药物的中枢γ-氨基丁酸能受体外,还在内分泌类固醇生成组织、免疫器官和细胞(如巨噬细胞和淋巴细胞)中鉴定出了这些分子的外周型结合位点(PBR)。据报道,PBR激活会降低先天免疫和宿主防御能力。本实验旨在分析地西泮对艾氏腹水瘤生长以及对荷艾氏腹水瘤小鼠巨噬细胞活性的影响。结果显示,地西泮(3.0毫克/千克/天,连续7天)增加了艾氏腹水瘤细胞数量和肿瘤诱导的腹水体积。较小剂量的地西泮未观察到这些作用,提示存在剂量依赖性效应。此外,我们的结果表明,每天给予3.0毫克/千克的地西泮,连续2天,会降低:(1)注射艾氏腹水瘤后回收的腹膜白细胞数量;(2)巨噬细胞铺展百分比;(3)巨噬细胞一氧化氮产生水平。地西泮(3.0毫克/千克/天,连续2天)对巨噬细胞吞噬作用或过氧化氢产生没有影响。本文基于地西泮的直接和/或间接作用对这些数据进行了讨论。特别是,我们的发现可能是由于地西泮对巨噬细胞和肿瘤细胞上存在的PBR有直接作用,或者仍可能由下丘脑-垂体-肾上腺(HPA)轴内的PBR刺激介导。