Morrison L D, Smith D D, Kish S J
Human Neurochemical Pathology Laboratory, Clarke Institute of Psychiatry, University of Toronto, Ontario, Canada.
J Neurochem. 1996 Sep;67(3):1328-31. doi: 10.1046/j.1471-4159.1996.67031328.x.
S-Adenosylmethionine is an essential ubiquitous metabolite central to many biochemical pathways, including transmethylation and polyamine biosynthesis. Reduced CSF S-adenosylmethionine levels in Alzheimer's disease have been reported; however, no information is available regarding the status of S-adenosylmethionine or S-adenosylmethionine-dependent methylation in the brain of patients with this disorder. S-Adenosylmethionine concentrations were measured in postmortem brain of 11 patients with Alzheimer's disease. We found decreased levels of S-adenosylmethionine (-67 to -85%) and its demethylated product S-adenosylhomocysteine (-56 to -79%) in all brain areas examined (cerebral cortical subdivisions, hippocampus, and putamen) as compared with matched controls (n = 14). S-Adenosylmethionine and S-adenosylhomocysteine levels were normal in occipital cortex of patients with idiopathic Parkinson's disease (n = 10), suggesting that the decreased S-adenosylmethionine levels in Alzheimer's disease are not simply a consequence of a chronic, neurodegenerative condition. Reduced S-adenosylmethionine levels could be due to excessive utilization in polyamine biosynthesis. The severe reduction in levels of this essential biochemical substrate would be expected to compromise seriously metabolism and brain function in patients with Alzheimer's disease and may provide the basis for the observations of improved cognition in some Alzheimer's patients following S-adenosylmethionine therapy.
S-腺苷甲硫氨酸是一种必需的普遍存在的代谢产物,是许多生化途径的核心,包括转甲基作用和多胺生物合成。已有报道称阿尔茨海默病患者脑脊液中S-腺苷甲硫氨酸水平降低;然而,关于该疾病患者大脑中S-腺苷甲硫氨酸或S-腺苷甲硫氨酸依赖性甲基化状态尚无相关信息。对11例阿尔茨海默病患者的死后大脑进行了S-腺苷甲硫氨酸浓度测定。我们发现,与匹配的对照组(n = 14)相比,在所检查的所有脑区(大脑皮质亚区、海马体和壳核)中,S-腺苷甲硫氨酸水平降低了67%至85%,其去甲基化产物S-腺苷同型半胱氨酸水平降低了56%至79%。特发性帕金森病患者(n = 10)枕叶皮质中的S-腺苷甲硫氨酸和S-腺苷同型半胱氨酸水平正常,这表明阿尔茨海默病患者S-腺苷甲硫氨酸水平降低并非仅仅是慢性神经退行性疾病的结果。S-腺苷甲硫氨酸水平降低可能是由于在多胺生物合成中过度利用。这种必需生化底物水平的严重降低预计会严重损害阿尔茨海默病患者的代谢和脑功能,并可能为一些阿尔茨海默病患者接受S-腺苷甲硫氨酸治疗后认知改善的观察结果提供依据。