Lange K W, Youdim M B, Riederer P
Department of Clinical Neurochemistry, University of Würzburg, Federal Republic of Germany.
J Neural Transm Suppl. 1992;38:27-44.
Recent findings of impaired mitochondrial function, altered iron metabolism and increased lipid peroxidation in the substantia nigra in Parkinson's disease emphasize the significance of oxidative stress and free radical formation in the pathogenesis of the disease. Future research will focus on improvements in neuroprotective therapy to prevent or slow the rate of progression of Parkinson's disease. Possible neuroprotective strategies include free radical scavengers, monoamine oxidase-B inhibitors, iron chelators and glutamate antagonists.
帕金森病患者黑质线粒体功能受损、铁代谢改变及脂质过氧化增加的最新研究结果,凸显了氧化应激和自由基形成在该疾病发病机制中的重要性。未来的研究将聚焦于改善神经保护疗法,以预防或减缓帕金森病的进展速度。可能的神经保护策略包括自由基清除剂、单胺氧化酶B抑制剂、铁螯合剂和谷氨酸拮抗剂。