Ono S, Cai L, Cherian M G
Department of Pathology, Health Sciences Centre, University of Western Ontario, London, Canada.
Radiat Res. 1998 Jul;150(1):52-7.
The induction of metallothionein (MT) synthesis in the brain was investigated in MT-I isoform-overexpressing transgenic (MT-I*) and control mice after exposure to increasing doses of 2 to 20 Gy of whole-body gamma radiation. Although the MT-I isoform was the major isoform of MT in this transgenic mouse, the other isoforms, MT-II and MT-III, were also present in the brain. The total concentration of MT in the brain was measured by a cadmium-binding assay, while zinc and lipid peroxides were measured by atomic absorption spectrophotometry and by the thiobarbituric acid method, respectively. In MT-I* mice at 24 h after radiation exposure, the level of MT in the brain was increased from a basal level of 44.4 +/- 4.0 microg/g to a maximum level of 91.0 +/- 9.0 microg/g after 5 Gy and remained high after 10 and 20 Gy. In a time-course experiment with 5 Gy, the concentration of MT in the brain of MT-I* mice increased at 3 h and reached a maximum of 175.3 +/- 15.3 microg/g at 6 h. This high level of MT remained unchanged for 48 h after radiation exposure. Metallothionein was not induced markedly in the brains of control mice either at 24 h after exposure to 2-20 Gy gamma radiation or at different times after exposure to 5 Gy gamma radiation. In both strains of mice, the total concentration of zinc in the brain decreased with increasing radiation dose. No differences in lipid peroxide levels were seen in control mice exposed to 5 Gy at 6 and 12 h or after exposure to three other doses (2, 10 and 20 Gy) at 24 h. Slight increases (1.35 and 1.22, respectively) in lipid peroxide levels were observed in control mice at 24 and 48 h after exposure to 5 Gy. Lipid peroxide levels in the brain were not changed in irradiated MT-I* mice. The results show a marked increase in the levels of MT in the brain of transgenic mice after exposure to gamma radiation. The induced synthesis of MT may be only one of several mechanisms that prevent the induction of lipid peroxidation in the brain by gamma radiation.
在全身接受2至20 Gy递增剂量的γ射线照射后,对金属硫蛋白-I(MT-I)亚型过表达的转基因小鼠(MT-I*)和对照小鼠大脑中金属硫蛋白(MT)合成的诱导情况进行了研究。尽管MT-I亚型是该转基因小鼠中MT的主要亚型,但其他亚型MT-II和MT-III在大脑中也有存在。通过镉结合测定法测量大脑中MT的总浓度,而锌和脂质过氧化物分别通过原子吸收分光光度法和硫代巴比妥酸法进行测量。在辐射暴露后24小时,MT-I小鼠大脑中MT的水平从基础水平44.4±4.0微克/克增加到5 Gy后的最高水平91.0±9.0微克/克,并在10 Gy和20 Gy后保持高水平。在5 Gy的时间进程实验中,MT-I小鼠大脑中MT的浓度在3小时增加,并在6小时达到最高值175.3±15.3微克/克。辐射暴露后48小时,这种高水平的MT保持不变。在暴露于2 - 20 Gyγ射线后24小时或暴露于5 Gyγ射线后的不同时间,对照小鼠大脑中的MT均未明显诱导。在两种品系的小鼠中,大脑中锌的总浓度均随辐射剂量增加而降低。在暴露于5 Gy后6小时和12小时或暴露于其他三种剂量(2、10和20 Gy)后24小时的对照小鼠中,脂质过氧化物水平未见差异。在暴露于5 Gy后24小时和48小时的对照小鼠中,观察到脂质过氧化物水平略有增加(分别为1.35和1.22)。照射后的MT-I*小鼠大脑中的脂质过氧化物水平未发生变化。结果表明,转基因小鼠在暴露于γ射线后大脑中MT水平显著增加。MT的诱导合成可能只是防止γ射线诱导大脑脂质过氧化的几种机制之一。