Department of Radiology and Medical Physics, Kashan University of Medical Sciences, Kashan, Iran.
Mutat Res. 2012 Oct-Nov;738-739:19-27. doi: 10.1016/j.mrfmmm.2012.08.006. Epub 2012 Sep 7.
The close relationship between free radicals effects and apoptosis process has been proved. Melatonin has been reported as a direct free radical scavenger. We investigated the capability of melatonin in the modification of radiation-induced apoptosis and apoptosis-associated upstream regulators expression in rat peripheral blood lymphocytes. Rats were irradiated with a single whole body Cobalt 60-gamma radiation dose of 8Gy at a dose rate of 101cGy/min with or without melatonin pretreatments at different concentrations of 10 and 100mg/kg body weight. The rats were divided into eight groups of control, irradiation-only, vehicle-only, vehicle plus irradiation, 10mg/kg melatonin alone, 10mg/kg melatonin plus irradiation, 100mg/kg melatonin alone and 100mg/kg melatonin plus irradiation. Rats were given an intraperitoneal (IP) injection of melatonin or the same volume of vehicle alone 1h prior to irradiation. Blood samples were taken 4, 24, 48 and 72h after irradiation for evaluation of flow cytometric analysis of apoptotic lymphocytes using Annexin V/PI assay and measurement of bax and bcl-2 expression using quantitative real-time PCR (RT(2)qPCR). Irradiation-only and vehicle plus irradiation showed an increase in the percentage of apoptotic lymphocytes significantly different from control group (P<0.01), while melatonin pretreatments in a dose-dependent manner reduced it as compared with the irradiation-only and vehicle plus irradiation groups (P<0.01) in all time points. This reduced apoptosis by melatonin was related to the downregulation of bax, upregulation of bcl-2, and therefore reduction of bax/bcl-2 ratio. Our results suggest that melatonin in these doses may provide modulation of bax and bcl-2 expression as well as bax/bcl-2 ratio to protect rat peripheral blood lymphocytes from gamma irradiation-induced apoptosis.
自由基效应与细胞凋亡过程之间的密切关系已得到证实。褪黑素已被报道为一种直接的自由基清除剂。我们研究了褪黑素在修饰辐射诱导的细胞凋亡和凋亡相关上游调节因子表达方面的能力,这些研究是在大鼠外周血淋巴细胞中进行的。大鼠接受单次全身钴 60-γ射线照射,剂量率为 101cGy/min,照射剂量为 8Gy,同时或不同浓度(10 和 100mg/kg 体重)的褪黑素预处理。大鼠分为对照组、单纯照射组、单纯溶剂组、溶剂加照射组、10mg/kg 褪黑素组、10mg/kg 褪黑素加照射组、100mg/kg 褪黑素组和 100mg/kg 褪黑素加照射组。照射前 1h,大鼠腹腔内(IP)注射褪黑素或等量溶剂。照射后 4、24、48 和 72h 采血,采用 Annexin V/PI 法评估凋亡淋巴细胞的流式细胞分析,采用实时定量 PCR(RT(2)qPCR)测量 bax 和 bcl-2 的表达。单纯照射组和溶剂加照射组与对照组相比,凋亡淋巴细胞的百分比显著增加(P<0.01),而褪黑素预处理呈剂量依赖性降低,与单纯照射组和溶剂加照射组相比(P<0.01)在所有时间点均如此。褪黑素降低凋亡与 bax 下调、bcl-2 上调有关,因此 bax/bcl-2 比值降低。我们的结果表明,这些剂量的褪黑素可能通过调节 bax 和 bcl-2 表达以及 bax/bcl-2 比值来保护大鼠外周血淋巴细胞免受γ射线诱导的凋亡。