Ríos C, Tapia R
Neurosci Lett. 1987 Jun 26;77(3):321-6. doi: 10.1016/0304-3940(87)90521-0.
We studied the effect of the Parkinson-inducing drug 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and of its metabolite 1-methyl-4-phenylpyridinium (MPP+) on lipid peroxidation in mouse brain homogenates in vitro. MPTP (0.35-1.4 mM) inhibited both spontaneous and Fe2+-induced peroxidation in a dose-dependent manner. MPP+, on the other hand, produced a slight enhancement of lipid peroxidation at 1.4 and 2.1 mM concentrations. These results are discussed in terms of the possible mechanisms of MPTP and MPP+ neurotoxicity.
我们研究了诱发帕金森病的药物1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)及其代谢产物1-甲基-4-苯基吡啶鎓(MPP+)对体外小鼠脑匀浆中脂质过氧化的影响。MPTP(0.35 - 1.4 mM)以剂量依赖的方式抑制自发的和Fe2+诱导的过氧化反应。另一方面,MPP+在1.4和2.1 mM浓度时使脂质过氧化略有增强。根据MPTP和MPP+神经毒性的可能机制对这些结果进行了讨论。