Transcriptome analysis in a rat model of L-DOPA-induced dyskinesia

被引:130
作者
Konradi, C
Westin, JE
Carta, M
Eaton, ME
Kuter, K
Dekundy, A
Lundblad, M
Cenci, MA
机构
[1] McLean Hosp, Mailman Res Ctr, Lab Neuoplast, Belmont, MA 02478 USA
[2] Harvard Univ, Sch Med, Dept Psychiat, Boston, MA 02115 USA
[3] Univ Cagliari, Dept Appl Sci Biosyst, Div Human Physiol, Cagliari, Italy
[4] Wallenberg Neurosci Ctr, Dept Physiol Sci, Sect Basal Ganglia Pathophysiol, Lund, Sweden
[5] Polish Acad Sci, Inst Pharmacol, Dept Neuropsychopharmacol, Krakow, Poland
[6] Merz Pharmaceut, Dept Behav Pharmacol, D-60318 Frankfurt, Germany
关键词
L-DOPA; dyskinesia; Parkinson's disease; 6-hydroxydopamine; gene microarrays; striatum; calcium; ribosomes; ATPases; GABA;
D O I
10.1016/j.nbd.2004.07.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have examined the pattern of striatal messenger RNA expression of over 8000 genes in a rat model of levodopa (L-DOPA)-induced dyskinesia and Parkinson disease (PD). 6-Hydroxydopamine (6-OHDA)-lesioned rats were treated with L-DOPA or physiological saline for 22 days and repeatedly tested for antiakinetic response to L-DOPA and the development of abnormal involuntary movements (AIMs). In a comparison of rats that developed a dyskinetic motor response to rats that did not, we found striking differences in gene expression patterns. In rats that developed dyskinesia, GABA neurons had an increased transcriptional activity, and genes involved in Ca2+ homeostasis, in Ca2+-dependent signaling, and in structural and synaptic plasticity were upregulated. The gene expression patterns implied that the dyskinetic striatum had increased transcriptional, as well as synaptic activity, and decreased capacity for energy production. Some basic maintenance chores such as ribosome protein biosynthesis were downregulated, possibly a response to expended of ATP levels. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:219 / 236
页数:18
相关论文
共 80 条
[1]   Levodopa - Is toxicity a myth? [J].
Agid, Y .
NEUROLOGY, 1998, 50 (04) :858-863
[2]   Somatostatin receptor 2 knockout/lacZ knockin mice show impaired motor coordination and reveal sites of somatostatin action within the striatum [J].
Allen, JP ;
Hathway, GJ ;
Clarke, NJ ;
Jowett, MI ;
Topps, S ;
Kendrick, KM ;
Humphrey, PPA ;
Wilkinson, LS ;
Emson, PC .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 17 (09) :1881-1895
[3]   CNS energy metabolism as related to function [J].
Ames, A .
BRAIN RESEARCH REVIEWS, 2000, 34 (1-2) :42-68
[4]   Striatal fosB expression is causally linked with L-DOPA-induced abnormal involuntary movements and the associated upregulation of striatal prodynorphin mRNA in a rat model of Parkinson's disease [J].
Andersson, M ;
Hilbertson, A ;
Cenci, MA .
NEUROBIOLOGY OF DISEASE, 1999, 6 (06) :461-474
[5]   cAMP response element-binding protein is required for dopamine-dependent gene expression in the intact but not the dopamine-denervated striatum [J].
Andersson, M ;
Konradi, C ;
Cenci, MA .
JOURNAL OF NEUROSCIENCE, 2001, 21 (24) :9930-9943
[6]   Neurotoxicity associated with neuroleptic-induced oral dyskinesias in rats - Implications for tardive dyskinesia? [J].
Andreassen, OA ;
Jorgensen, HA .
PROGRESS IN NEUROBIOLOGY, 2000, 61 (05) :525-541
[7]   14-3-3 proteins in the nervous system [J].
Berg, D ;
Holzmann, C ;
Riess, O .
NATURE REVIEWS NEUROSCIENCE, 2003, 4 (09) :752-762
[8]   Pathophysiology of levodopa-induced dyskinesia: Potential for new therapies [J].
Bezard, E ;
Brotchie, JM ;
Gross, CE .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (08) :577-588
[9]  
Blaustein MP, 2002, ANN NY ACAD SCI, V976, P356
[10]   CB1 cannabinoid receptor signalling in Parkinson's disease [J].
Brotchie, JM .
CURRENT OPINION IN PHARMACOLOGY, 2003, 3 (01) :54-61