Kojima S, Matsuki O, Nomura T, Shimura N, Kubodera A, Yamaoka K, Tanooka H, Wakasugi H, Honda Y, Honda S, Sasaki T
Research Institute for Biological Sciences, Science University of Tokyo, 2669 Yamazaki, Noda-shi, Chiba 278-0022, Japan.
Brain Res. 1998 Oct 19;808(2):262-9. doi: 10.1016/s0006-8993(98)00832-4.
First, we determined the cerebral localization of reduced glutathione (GSH) in normal mice by means of autoradiography using 99mTc-meso-hexamethyl propylene oxime. A highly specific localization of GSH in the cerebellum and hippocampus was observed. Secondly, we measured the elevation of GSH level in the brain after low-dose gamma-irradiation. The cerebral GSH levels increased soon after irradiation with 50 cGy of gamma-rays, reaching a maximum at 3 h post-treatment, then remaining significantly higher than that of the non-irradiated control until 12 h and returning to the control level by 24 h. Thirdly, we examined the induction of the activities and the mRNAs of proteins involved in the synthesis and regeneration of GSH in the brain of mice subjected to low-dose gamma-ray irradiation. The level of mRNA for gamma-glutamylcysteine synthetase was significantly increased at 0.5 h, and remained high until 2 h post-irradiation (50 cGy). The level was transiently lowered to the non-irradiated control level at 3 h and slightly increased again after 6 h post-irradiation. gamma-Glutamylcysteine synthetase activity was significantly increased 3 h after irradiation, and remained high up to 24 h post-irradiation. As for glutathione reductase, the mRNA level was increased at 0.5 h, and peaked strongly at 2 h, while the enzyme activity was significantly increased at 6 h after irradiation, and continued to increase up to 24 h. The level of mRNA for thioredoxin, which contributes to GSH biosynthesis by supplying cysteine to the de novo pathway, peaked between 0.5 h and 2 h post-irradiation, and rapidly declined thereafter. The content of thioredoxin showed a transient decrease immediately after irradiation, but was then remarkably elevated, reaching a maximum at 3 h, and thereafter declining sharply. These results indicate that the increase in endogenous GSH in mouse brain soon after low-dose gamma-ray irradiation is a consequence of the induction of GSH synthesis-related proteins and occurs via both the de novo synthesis and the regeneration pathways.
首先,我们通过使用99mTc-内消旋六甲基丙烯肟的放射自显影法确定了正常小鼠体内还原型谷胱甘肽(GSH)的脑定位。观察到GSH在小脑和海马中有高度特异性的定位。其次,我们测量了低剂量γ射线照射后大脑中GSH水平的升高。用50 cGy的γ射线照射后,大脑GSH水平在照射后很快升高,在治疗后3小时达到最大值,然后在12小时内显著高于未照射的对照组,并在24小时恢复到对照水平。第三,我们研究了低剂量γ射线照射的小鼠大脑中参与GSH合成和再生的蛋白质的活性和mRNA的诱导情况。γ-谷氨酰半胱氨酸合成酶的mRNA水平在0.5小时时显著升高,并在照射后(50 cGy)一直保持高水平直至2小时。该水平在3小时时短暂降至未照射对照组水平,并在照射后6小时再次略有升高。γ-谷氨酰半胱氨酸合成酶活性在照射后3小时显著增加,并在照射后24小时内一直保持高水平。至于谷胱甘肽还原酶,mRNA水平在0.5小时时升高,并在2小时时强烈峰值,而酶活性在照射后6小时显著增加,并持续增加直至24小时。硫氧还蛋白的mRNA水平在照射后0.5小时至2小时之间达到峰值,此后迅速下降,硫氧还蛋白通过为从头合成途径提供半胱氨酸而有助于GSH生物合成。硫氧还蛋白的含量在照射后立即短暂下降,但随后显著升高,在3小时时达到最大值,此后急剧下降。这些结果表明,低剂量γ射线照射后小鼠大脑中内源性GSH的增加是GSH合成相关蛋白诱导的结果,并且通过从头合成和再生途径发生。