Segura-Aguilar J, Metodiewa D, Baez S
Programme of Molecular and Clinical Pharmacology, ICBM, Faculty of Medicine, University of Chile, Casilla, Santiago.
Neurotox Res. 2001 Apr;3(2):157-65. doi: 10.1007/BF03033188.
We present for discussion a possible molecular mechanism explaining the formation of reactive oxygen species involved in the neurodegenerative process of dopaminergic system in Parkinson's disease. This new hypothesis involves one-electron reduction of aminochrome to o-semiquinone radical, which seems to be the reaction responsible for neurodegenerative process of dopaminergic system. Leukoaminochrome o-semiquinone is extremely reactive with oxygen, which reoxidizes by reducing oxygen to superoxide radicals. Superoxide radicals enzymatically or spontaneously dismutate to dioxygen and hydrogen peroxide which is a precursor of hydroxyl radicals. ESR-experiments have showed that aminochrome o-semiquinone is extremely reactive in the presence of oxygen compared to dopamine o-semiquinone. In addition, the antioxidant enzymes superoxide dismutase and catalase play a prooxidant role by increasing the autoxidation rate and formation of superoxide radicals. One electron reduction of aminochrome to o-semiquinone can be performed by flavoenzymes which use NADPH and NADH as electron donator. The ability of aminochrome o-semiquinone to autoxidize in the presence of oxygen gives rise to a redox cycling process which will continue until oxygen, NADH and/or NADPH are depleted. Depletion of NADPH will prevent glutathione reductase from reducing glutathione, which is one of the main antioxidants in the cell. In addition depletion of NADH will prevent the formation of ATP in the electron transport chain in the mitochondria. Two antioxidants, probably, neuroprotective reactions are also discussed.
我们提出一种可能的分子机制以供讨论,该机制解释了帕金森病中多巴胺能系统神经退行性过程中活性氧物种的形成。这个新假说涉及氨基色素单电子还原为邻半醌自由基,这似乎是多巴胺能系统神经退行性过程的关键反应。白细胞氨基色素邻半醌与氧反应性极强,它通过将氧还原为超氧自由基而重新氧化。超氧自由基可通过酶促或自发歧化生成二氧和过氧化氢,而过氧化氢是羟基自由基的前体。电子顺磁共振实验表明,与多巴胺邻半醌相比,氨基色素邻半醌在有氧存在时反应性极强。此外,抗氧化酶超氧化物歧化酶和过氧化氢酶通过提高自氧化速率和超氧自由基的形成而发挥促氧化作用。氨基色素单电子还原为邻半醌可由以烟酰胺腺嘌呤二核苷酸磷酸(NADPH)和烟酰胺腺嘌呤二核苷酸(NADH)作为电子供体的黄素酶来完成。氨基色素邻半醌在有氧存在时自氧化的能力引发了一个氧化还原循环过程,该过程将持续到氧、NADH和/或NADPH耗尽。NADPH的耗尽将阻止谷胱甘肽还原酶还原谷胱甘肽,而谷胱甘肽是细胞中的主要抗氧化剂之一。此外,NADH的耗尽将阻止线粒体电子传递链中三磷酸腺苷(ATP)的形成。文中还讨论了两种可能具有神经保护作用的抗氧化剂反应。