Margaglione M, Garofano R, Cirillo F, Ruocco A, Grandone E, Vecchione G, Milan G, Di Minno G, De Blasi A, Postiglione A
I.R.R.C.S. Casa Sollievo della Sofferenza, S. Giovanni Rotondo, Foggia, Italy.
Aging (Milano). 1995 Feb;7(1):49-54. doi: 10.1007/BF03324292.
Chromosome 21 contains genes whose altered expression has long been associated with Down's syndrome and whose altered structure with some cases of Alzheimer's disease (AD). The gene for the Cu/Zn superoxide dismutase enzyme (SOD-1), a key enzyme in the metabolism of oxygen free radicals, is located on the distal portion of chromosome 21. Due to the triplication of the SOD-1 gene, patients with Down's syndrome have an almost 50% increase in their SOD activity. On the other hand, almost 25% of the patients with Down's syndrome over 40 years of age develop progressive dementia, with clinical symptoms of AD. Therefore, we decided to evaluate whether abnormalities in the production of free radicals could be detected in blood cells from AD patients, and whether they correlated with molecular variations in the Cu/Zn SOD-1 gene. Superoxide anion production was evaluated spectrophotometrically in suspensions of monocytes from 9 sporadic AD patients, and from 9 aged-matched apparently normal controls. After stimulation with increasing concentrations of n-formyl-methionyl-leucyl-phenylalanine (fMLP) or Ca ionophore A23187, monocyte free radical generation was quantitatively and qualitatively normal. Furthermore, restriction fragment length polymorphism (RFLP) analysis of leukocyte DNA digested with a variety of enzymes, gave comparable results in patients and controls. Our data support the possibility that in addition to the generation of free radicals, other directions should be explored to elucidate the mechanisms of dementia in AD.
21号染色体包含一些基因,其表达改变长期以来一直与唐氏综合征相关,其结构改变则与某些阿尔茨海默病(AD)病例相关。铜/锌超氧化物歧化酶(SOD-1)基因是氧自由基代谢中的关键酶,位于21号染色体的远端。由于SOD-1基因的三倍体现象,唐氏综合征患者的SOD活性几乎增加了50%。另一方面,40岁以上的唐氏综合征患者中近25%会发展为进行性痴呆,出现AD的临床症状。因此,我们决定评估是否能在AD患者的血细胞中检测到自由基产生异常,以及它们是否与铜/锌SOD-1基因的分子变异相关。用分光光度法评估了9例散发性AD患者和9例年龄匹配的明显正常对照者的单核细胞悬液中超氧阴离子的产生。在用浓度递增的n-甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)或钙离子载体A23187刺激后,单核细胞自由基的产生在数量和质量上均正常。此外,用多种酶消化白细胞DNA后的限制性片段长度多态性(RFLP)分析在患者和对照中得到了类似结果。我们的数据支持这样一种可能性,即除了自由基的产生外,还应探索其他方向来阐明AD中痴呆的机制。