Kumar U, Dunlop D M, Richardson J S
Department of Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Life Sci. 1994;54(24):1855-60. doi: 10.1016/0024-3205(94)90142-2.
Many of the biological abnormalities seen in samples of the brain and other tissues from patients with Alzheimer's disease, are consistent with an excessive action of oxygenic free radicals. Mitochondria from fibroblasts grown in tissue culture from skin samples taken at autopsy from patients with histologically confirmed Alzheimer's disease, take up significantly less calcium than do fibroblast mitochondria from age matched non-demented controls. Following exposure to oxygenic free radicals generated by adding ferrous ions to the incubation mixture, calcium uptake is increased to a greater extent in Alzheimer's mitochondria than in controls. At the doses used, pretreatment with the lazaroid antioxidant drug U-74500A, or with the iron chelator deferoxamine, prevents the free radical induced increase in calcium uptake by control mitochondria, but provides only partial protection for Alzheimer's mitochondria. These observations suggest that Alzheimer's fibroblast mitochondria have impaired calcium transport processes and show increased sensitivity to oxygenic free radicals.
在阿尔茨海默病患者的大脑及其他组织样本中观察到的许多生物学异常现象,都与氧自由基的过度作用相一致。从经组织学确诊为阿尔茨海默病的患者尸检时采集的皮肤样本在组织培养中生长的成纤维细胞线粒体,其摄取的钙明显少于年龄匹配的非痴呆对照者的成纤维细胞线粒体。在孵育混合物中添加亚铁离子产生氧自由基后,阿尔茨海默病线粒体中的钙摄取量比对照组增加的幅度更大。在所使用的剂量下,用拉扎罗类抗氧化药物U - 74500A或铁螯合剂去铁胺预处理,可防止自由基诱导对照线粒体钙摄取增加,但对阿尔茨海默病线粒体仅提供部分保护。这些观察结果表明,阿尔茨海默病成纤维细胞线粒体的钙转运过程受损,且对氧自由基表现出更高的敏感性。