Serum interleukin (IL-2, IL-10, IL-6, IL-4), TNFα, and INFγ concentrations are elevated in patients with atypical and idiopathic parkinsonism

被引:298
作者
Brodacki, Bogdan [2 ]
Staszewski, Jacek [2 ]
Toczylowska, Beata [3 ,4 ]
Kozlowska, Ewa [5 ]
Drela, Nadzieja [5 ]
Chalimoniuk, Malgorzata [1 ]
Stepien, Adam [2 ]
机构
[1] Polish Acad Sci, Med Res Ctr, Dept Cellular Signaling, PL-02106 Warsaw, Poland
[2] Mil Inst Hlth Serv, Dept Neurol, Warsaw, Poland
[3] Polish Acad Sci, Inst Biochem & Biophys, PL-02106 Warsaw, Poland
[4] Polish Acad Sci, Inst Biocybernet & Biomed Engn, PL-02106 Warsaw, Poland
[5] Univ Warsaw, Div Biol, Dept Immunol, Warsaw, Poland
关键词
cytokines; atypical parkinsonism; idiopathic Parkinson disease; serum;
D O I
10.1016/j.neulet.2008.06.040
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
We investigated serum levels of interleukin (IL)-2, IL-10, IL-6. IL-4, TNF alpha, INF gamma in 7 patients with atypical parkinsonism (AP), 31 idiopathic PD (iPD) patients, 17 idiopathic PD with cardiovascular risk factor (iPD-CVRF) patients, and 20 age-matched controls (healthy, non-parkinsonian patients). Cytokine concentrations were measured using the Becton Dickinson (TM) (BD (TM)) human Th1/Th2 Cytokine kit 11 with a flow cytometry system. The concentrations of IL-2, IL-10, IL-4, IL-6, TNF alpha, and INF gamma were detectable in the serum from all groups, including the control. Increased serum IL-2, IL-10, IL-4, IL-6, TNF alpha, and INF gamma concentrations were found in all groups of parkinsonian patients, as compared to the control group. The highest elevations of serum IL-2, IL-4, IL-6, TNF alpha, and INF gamma concentrations were observed in AP patients, as compared to the iPD and iPD-CVRF groups. However, the serum IL-6 concentration was higher in the iPD-CVRF group than in the iPD group. The IL-10 level was significantly higher in all groups of PD patients relative to the control group, but was the lowest in the serum from the AP patients. Moreover, the serum levels of lipid peroxidation products were enhanced 2.1 - and 1.5-fold in AP and both iPD groups, respectively. These results argue in favor of the involvement of immunological events in the process of neurodegeneration in AP and PD. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:158 / 162
页数:5
相关论文
共 32 条
[1]
[Anonymous], 1989, Quantification of Neurological Deficit
[2]
ASAKAWA T, 1980, LIPIDS, V15, P137, DOI 10.1007/BF02540959
[3]
Entry of blood-borne cytokines into the central nervous system: Effects on cognitive processes [J].
Banks, WA ;
Farr, SA ;
Morley, JE .
NEUROIMMUNOMODULATION, 2002, 10 (06) :319-327
[4]
Neurodegenerative diseases and oxidative stress [J].
Barnham, KJ ;
Masters, CL ;
Bush, AI .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (03) :205-214
[5]
Experimental models of Parkinson's disease [J].
Beal, MF .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (05) :325-332
[6]
DIFFERENTIAL VULNERABILITY OF CHOLINERGIC PROJECTIONS TO THE MEDIODORSAL NUCLEUS OF THE THALAMUS IN SENILE DEMENTIA OF ALZHEIMER TYPE AND PROGRESSIVE SUPRANUCLEAR PALSY [J].
BRANDEL, JP ;
HIRSCH, EC ;
MALESSA, S ;
DUYCKAERTS, C ;
CERVERA, P ;
AGID, Y .
NEUROSCIENCE, 1991, 41 (01) :25-31
[7]
CHUNG IY, 1990, J IMMUNOL, V144, P2999
[8]
Fahn S, 2000, MERRITTS NEUROLOGY, P679
[9]
Gilman S, 1998, J AUTONOM NERV SYST, V74, P189
[10]
PARKINSONISM - ONSET PROGRESSION AND MORTALITY [J].
HOEHN, MM ;
YAHR, MD .
NEUROLOGY, 1967, 17 (05) :427-&