Wüllner U, Löschmann P A, Schulz J B, Schmid A, Dringen R, Eblen F, Turski L, Klockgether T
Department of Neurology, Eberhard-Karls-University, Tübingen, Germany.
Neuroreport. 1996 Mar 22;7(4):921-3. doi: 10.1097/00001756-199603220-00018.
Glutathione levels are decreased in the substantia nigra of patients with Parkinson's disease. We studied whether glutathione depletion contributes to dopaminergic cell death using a specific inhibitor of glutathione biosynthesis, L-buthionine sulfoximine (BSO). We found no significant reduction of tyrosine hydroxylase-positive cells in the substantia nigra pars compacta (SNpc) when BSO was administered systemically to preweanling mice or locally to the SNpc of adult rats. However, the combination of BSO with MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) in preweanling mice and the combination of nigral injections of BSO with intrastriatal injections of MPP+ (1-methyl-4-phenylpyridinium), the active metabolite of MPTP in adult rats, potentiated the toxic effects of MPTP and MPP+ on nigral neurones. Our data show that glutathione depletion can result in cell death if the nigrostriatal system is metabolically compromised.
帕金森病患者黑质中的谷胱甘肽水平降低。我们使用谷胱甘肽生物合成的特异性抑制剂L-丁硫氨酸亚砜胺(BSO)研究了谷胱甘肽耗竭是否导致多巴胺能细胞死亡。当对断奶前小鼠全身给药BSO或对成年大鼠黑质致密部(SNpc)局部给药时,我们发现SNpc中酪氨酸羟化酶阳性细胞没有显著减少。然而,在断奶前小鼠中BSO与MPTP(1-甲基-4-苯基-1,2,3,6-四氢吡啶)联合使用,以及在成年大鼠中黑质注射BSO与纹状体内注射MPTP的活性代谢产物MPP +(1-甲基-4-苯基吡啶鎓)联合使用,增强了MPTP和MPP +对黑质神经元的毒性作用。我们的数据表明,如果黑质纹状体系统代谢受损,谷胱甘肽耗竭会导致细胞死亡。