Striatal increase of extracellular dopamine levels during dystonic episodes in a genetic model of paroxysmal dyskinesia

被引:33
作者
Hamann, M [1 ]
Richter, A [1 ]
机构
[1] Free Univ Berlin, Inst Pharmacol & Toxicol, Sch Vet Med, D-14195 Berlin, Germany
关键词
basal ganglia; caudate putamen; dystonia; microdialysis; movement disorders; monoamines;
D O I
10.1016/j.nbd.2004.01.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In vivo microdialysis was used to examine the levels of dopamine, serotonin, and their metabolites dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), and 5-hydroxyindoleacetic acid (5-HIAA) in the striatum of dt(sz) mutant hamsters, an animal model of paroxysmal dyskinesia, in which stress can precipitate dystonic episodes. Measurements were made under three different conditions in each animal: (1) at baseline in the absence of abnormal involuntary movements, (2) during an episode of paroxysmal dystonia precipitated by handling, and (3) during the recovery (postdystonic) period. In comparison to nondystonic control hamsters, which were treated in the same manner as dystonic animals, no changes could be detected under basal conditions, although the levels of DOPAC and HVA tended to be higher in mutant hamsters. Significantly elevated striatal levels of dopamine and DOPAC became evident during the period of stress-induced dystonic attacks in mutant hamsters. During dystonic episodes, dopamine levels were approximately 6.5-fold higher (followed by a 2.5-fold increase of DOPAC) in dt(sz) hamsters than in normal controls. Before the disappearance of dystonia, the levels of dopamine returned to basal concentrations in mutant hamsters. Consistent with previous pharmacologic findings, paroxysmal dystonia in mutant hamsters is associated with temporary increases of extracellular dopamine levels in the striatum. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:78 / 84
页数:7
相关论文
共 47 条
[1]   DIFFERENTIAL EFFECT OF STRESS ON INVIVO DOPAMINE RELEASE IN STRIATUM, NUCLEUS ACCUMBENS, AND MEDIAL FRONTAL-CORTEX [J].
ABERCROMBIE, ED ;
KEEFE, KA ;
DIFRISCHIA, DS ;
ZIGMOND, MJ .
JOURNAL OF NEUROCHEMISTRY, 1989, 52 (05) :1655-1658
[2]   Selective decrease in central nervous system serotonin turnover in children with dopa-nonresponsive dystonia [J].
Assmann, B ;
Köhler, M ;
Hoffmann, GF ;
Heales, S ;
Surtees, R .
PEDIATRIC RESEARCH, 2002, 52 (01) :91-94
[3]   Dopamine transmission in DYT1 dystonia:: A biochemical and autoradiographical study [J].
Augood, SJ ;
Hollingsworth, Z ;
Albers, DS ;
Yang, L ;
Leung, JC ;
Muller, B ;
Klein, C ;
Breakefield, XO ;
Standaert, DG .
NEUROLOGY, 2002, 59 (03) :445-448
[4]   Further case of paroxysmal exercise-induced dystonia and some insights into pathogenesis [J].
Barnett, MH ;
Jarman, PR ;
Heales, SJR ;
Bhatia, KP .
MOVEMENT DISORDERS, 2002, 17 (06) :1386-1387
[5]   African states, bureaucratic culture and computer fixes [J].
Berman, BJ ;
Tettey, WJ .
PUBLIC ADMINISTRATION AND DEVELOPMENT, 2001, 21 (01) :1-13
[6]   Dose-dependent effect of ethanol on extracellular dopamine in mesolimbic striatum of awake rhesus monkeys: comparison with cocaine across individuals [J].
Bradberry, CW .
PSYCHOPHARMACOLOGY, 2002, 165 (01) :67-76
[7]   Expression of cholecystokinin, somatostatin, thyrotropin-releasing hormone, glutamic acid decarboxylase and tyrosine hydroxylase genes in the central nervous motor systems of the genetically dystonic hamster [J].
Burgunder, JM ;
Richter, A ;
Löscher, W .
EXPERIMENTAL BRAIN RESEARCH, 1999, 129 (01) :114-120
[8]   Attenuation and recovery of evoked overflow of striatal serotonin in rats treated with neurotoxic doses of methamphetamine [J].
Cass, WA .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (03) :1079-1085
[9]   PAROXYSMAL DYSKINESIAS - CLINICAL-FEATURES AND CLASSIFICATION [J].
DEMIRKIRAN, M ;
JANKOVIC, J .
ANNALS OF NEUROLOGY, 1995, 38 (04) :571-579
[10]  
Fahn S, 1988, Adv Neurol, V50, P1