Tórsdóttir G, Kristinsson J, Sveinbjörnsdóttir S, Snaedal J, Jóhannesson T
Department of Pharmacology and Toxicology, The Institute of Pharmacy, Pharmacology and Toxicology, University of Iceland.
Pharmacol Toxicol. 1999 Nov;85(5):239-43. doi: 10.1111/j.1600-0773.1999.tb02015.x.
In a previous study we found copper dyshomeostasis in patients with Alzheimer's disease. In this study, levels of copper in plasma, of ceruloplasmin in serum and ceruloplasmin oxidative activity as well as superoxide dismutase (SOD) activity in erythrocytes were determined in 40 patients with Parkinson's disease and their healthy age- and gender-matched controls. Copper concentrations did not differ significantly in the two groups, whereas both ceruloplasmin concentrations and ceruloplasmin oxidative activity were significantly lower in the patients, also relative to ceruloplasmin mass. SOD activity was not significantly different in the two groups but decreased significantly with the duration of disease. The same was found for ceruloplasmin oxidative activity. Ceruloplasmin oxidative activity and SOD activity did not decrease with age. Levels of serum iron, serum ferritin and total iron binding capacity were determined in about 30 of the patients and an equal number of controls and were not found to differ. Transferrin levels were significantly lower in the patients than in their controls but, conversely, the transferrin saturation was significantly higher in the patients. The results indicate that patients with Alzheimer's disease and Parkinson's disease have defective ceruloplasmin and SOD activities in common and that these defects are not necessarily associated with major disturbances in iron homeostasis.
在之前的一项研究中,我们发现阿尔茨海默病患者存在铜稳态失衡。在本研究中,测定了40例帕金森病患者及其年龄和性别匹配的健康对照者血浆中的铜水平、血清中的铜蓝蛋白水平和铜蓝蛋白氧化活性以及红细胞中的超氧化物歧化酶(SOD)活性。两组的铜浓度无显著差异,而患者的铜蓝蛋白浓度和铜蓝蛋白氧化活性均显著降低,相对于铜蓝蛋白质量也是如此。两组的SOD活性无显著差异,但随疾病持续时间显著降低。铜蓝蛋白氧化活性也是如此。铜蓝蛋白氧化活性和SOD活性不随年龄降低。在约30例患者和同样数量的对照者中测定了血清铁、血清铁蛋白和总铁结合力水平,未发现有差异。患者的转铁蛋白水平显著低于其对照者,但相反,患者的转铁蛋白饱和度显著更高。结果表明,阿尔茨海默病患者和帕金森病患者共同存在铜蓝蛋白和SOD活性缺陷,且这些缺陷不一定与铁稳态的重大紊乱相关。