DECREASED SERUM SELENIUM CONCENTRATIONS IN PATIENTS WITH PARKINSONS-DISEASE

被引:18
作者
JIMENEZJIMENEZ, FJ
MOLINA, JA
ARRIETA, FJ
AGUILAR, MV
CABRERAVALDIVIA, F
VAZQUEZ, A
JORGESANTAMARIA, A
SEIJAS, V
FERNANDEZCALLE, P
MARTINEZPARA, MC
机构
[1] HOSP UNIV PRINCIPE ASTURIAS, DEPT NEUROL, MADRID, SPAIN
[2] DOCE OCTUBRE, DEPT NEUROL, MADRID, SPAIN
[3] UNIV ALCALA DE HENARES, FAC PHARM, DEPT NUTR & BROMATOL, MADRID, SPAIN
[4] UNIV SAN CARLOS, DEPT NEUROL, MADRID, SPAIN
[5] CIUDAD SANIT LA PAZ, DEPT BIOCHEM, MADRID, SPAIN
关键词
GLUTATHIONE PEROXIDASE; OXIDATIVE STRESS; PARKINSONS DISEASE; SELENIUM; SERUM LEVELS;
D O I
10.1111/j.1468-1331.1995.tb00102.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Selenium is an essential component of the antioxidant enzyme glutathione peroxidase. The activity of this enzyme is reduced in the substantia nigra of patients with Parkinson's disease (PD), but the results of studies on erythrocytes are controversial. We compared the serum levels of selenium and the 24 h urinary selenium excretion (measured by hydride generation atomic absorption spectrophotometry) in 29 PD patients and 30 matched controls. Serum selenium levels were significantly lower in PD patients than in controls (34.6+/-2.35 and 45.2+/-3.83 mu g/l, p < 0.05) while urinary excretion was similar for both groups (47.1+/-6.25 and 45.5+/-5.38 mu g/24 h). These values were not influenced by antiparkinsonian drugs, and they did not correlate with age, age at onset and duration of the PD, scores of the Unified PD Rating Scale or the Hoehn and Yahr staging in the PD group. These results might suggest a possible role of low serum selenium levels in the risk for, or a consequence of the oxidative stress in PD.
引用
收藏
页码:111 / 114
页数:4
相关论文
共 19 条
[1]   BRAIN PEROXIDASE AND CATALASE IN PARKINSON DISEASE [J].
AMBANI, LM ;
VANWOERT, MH ;
MURPHY, S .
ARCHIVES OF NEUROLOGY, 1975, 32 (02) :114-118
[2]   THE POTENTIAL USE OF VITAMIN-E AND SELENIUM IN PARKINSONISM [J].
CADET, JL .
MEDICAL HYPOTHESES, 1986, 20 (01) :87-94
[3]   SELENIUM CONTENT AND DISTRIBUTION IN RAT-TISSUES IRRADIATED WITH GAMMA-RAYS [J].
DJUJIC, IS ;
JOZANOVSTANKOV, O ;
MANDIC, M ;
DEMAJO, M ;
VRVIC, MM .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1992, 33 :197-204
[4]   THE OXIDANT STRESS HYPOTHESIS IN PARKINSONS-DISEASE - EVIDENCE SUPPORTING IT [J].
FAHN, S ;
COHEN, G .
ANNALS OF NEUROLOGY, 1992, 32 (06) :804-812
[5]  
Fahn S. M. C., 1987, RECENT DEV PARKINSON, P153
[6]  
FERNANDEZPERIS E, 1986, SIGMA BASE DATOS BIO
[7]   OXIDANTS AND THE CENTRAL-NERVOUS-SYSTEM - SOME FUNDAMENTAL QUESTIONS - IS OXIDANT DAMAGE RELEVANT TO PARKINSONS-DISEASE, ALZHEIMERS-DISEASE, TRAUMATIC INJURY OR STROKE [J].
HALLIWELL, B .
ACTA NEUROLOGICA SCANDINAVICA, 1989, 80 :23-33
[8]   PARKINSONISM - ONSET PROGRESSION AND MORTALITY [J].
HOEHN, MM ;
YAHR, MD .
NEUROLOGY, 1967, 17 (05) :427-&
[9]   GLUTATHIONE-PEROXIDASE IN EARLY AND ADVANCED PARKINSONS-DISEASE [J].
JOHANNSEN, P ;
VELANDER, G ;
MAI, J ;
THORLING, EB ;
DUPONT, E .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1991, 54 (08) :679-682
[10]  
KERIMOV B F, 1991, Ukrainskii Biokhimicheskii Zhurnal, V63, P62