Gibson G E, Park L C, Sheu K F, Blass J P, Calingasan N Y
Department of Neurology and Neuroscience, Weill Medical College of Cornell University, Burke Medical Research Institute, White Plains, NY 10605, USA.
Neurochem Int. 2000 Feb;36(2):97-112. doi: 10.1016/s0197-0186(99)00114-x.
Altered energy metabolism is characteristic of many neurodegenerative disorders. Reductions in the key mitochondrial enzyme complex, the alpha-ketoglutarate dehydrogenase complex (KGDHC), occur in a number of neurodegenerative disorders including Alzheimer's Disease (AD). The reductions in KGDHC activity may be responsible for the decreases in brain metabolism, which occur in these disorders. KGDHC can be inactivated by several mechanisms, including the actions of free radicals (Reactive Oxygen Species, ROS). Other studies have associated specific forms of one of the genes encoding KGDHC (namely the DLST gene) with AD, Parkinson's disease, as well as other neurodegenerative diseases. Reductions in KGDHC activity can be plausibly linked to several aspects of brain dysfunction and neuropathology in a number of neurodegenerative diseases. Further studies are needed to assess mechanisms underlying the sensitivity of KGDHC to oxidative stress and the relation of KGDHC deficiency to selective vulnerability in neurodegenerative diseases.
能量代谢改变是许多神经退行性疾病的特征。关键的线粒体酶复合物α-酮戊二酸脱氢酶复合物(KGDHC)的活性降低发生在包括阿尔茨海默病(AD)在内的多种神经退行性疾病中。KGDHC活性的降低可能是这些疾病中脑代谢下降的原因。KGDHC可通过多种机制失活,包括自由基(活性氧,ROS)的作用。其他研究将编码KGDHC的基因之一(即DLST基因)的特定形式与AD帕金森病以及其他神经退行性疾病联系起来。在许多神经退行性疾病中,KGDHC活性的降低可能与脑功能障碍和神经病理学的几个方面有合理的联系。需要进一步研究以评估KGDHC对氧化应激敏感性的潜在机制以及KGDHC缺乏与神经退行性疾病中选择性易损性的关系。