Jeitner Thomas M, Xu Hui, Gibson Gary E
Department of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
J Neurochem. 2005 Jan;92(2):302-10. doi: 10.1111/j.1471-4159.2004.02868.x.
Abstract alpha-Ketoglutarate dehydrogenase (KGDHC) complex activity is diminished in a number of neurodegenerative disorders and its diminution in Alzheimer Disease (AD) is thought to contribute to the major loss of cerebral energy metabolism that accompanies this disease. The loss of KGDHC activity appears to be predominantly due to post-translation modifications. Thiamine deficiency also results in decreased KGDHC activity and a selective neuronal loss. Recently, myeloperoxidase has been identified in the activated microglia of brains from AD patients and thiamine-deficient animals. Myeloperoxidase produces a powerful oxidant, hypochlorous acid that reacts with amines to form chloramines. The aim of this study was to investigate the ability of hypochlorous acid and chloramines to inhibit the activity of KGDHC activity as a first step towards investigating the role of myeloperoxidase in AD. Hypochlorous acid and mono-N-chloramine both inhibited purified and cellular KGDHC and the order of inhibition of the purified complex was hypochlorous acid (1x) > mono-N-chloramine (approximately 50x) > hydrogen peroxide (approximately 1,500). The inhibition of cellular KGDHC occurred with no significant loss of cellular viability at all exposure times that were examined. Thus, hypochlorous acid and chloramines have the potential to inactivate a major target in neurodegeneration.
在多种神经退行性疾病中,α-酮戊二酸脱氢酶(KGDHC)复合体活性降低,其在阿尔茨海默病(AD)中的降低被认为是导致该疾病伴随的大脑能量代谢严重损失的原因。KGDHC活性的丧失似乎主要是由于翻译后修饰。硫胺素缺乏也会导致KGDHC活性降低和选择性神经元丢失。最近,在AD患者和硫胺素缺乏动物的大脑活化小胶质细胞中发现了髓过氧化物酶。髓过氧化物酶产生一种强大的氧化剂——次氯酸,次氯酸与胺反应形成氯胺。本研究的目的是研究次氯酸和氯胺抑制KGDHC活性的能力,作为研究髓过氧化物酶在AD中作用的第一步。次氯酸和一氯胺均抑制纯化的和细胞中的KGDHC,纯化复合体的抑制顺序为次氯酸(1倍)>一氯胺(约50倍)>过氧化氢(约1500倍)。在所检测的所有暴露时间下,细胞KGDHC的抑制均未伴随细胞活力的显著丧失。因此,次氯酸和氯胺有可能使神经退行性变中的一个主要靶点失活。