Tolerance to a suprathreshold dose of L-Dopa in MPTP mice: effects of glutamate antagonists

被引:23
作者
Fredriksson, A
Palomo, T
Chase, T
Archer, T
机构
[1] Univ Gothenburg, Dept Psychol, SE-40530 Gothenburg, Sweden
[2] Uppsala Univ, Dept Psychiat, Uppsala, Sweden
[3] Hosp 12 Octubre, Serv Psiquiatria, E-28041 Madrid, Spain
[4] NIH, Expt Therapeut Branch, Bethesda, MD 20892 USA
关键词
C57; Bl/6; mice; MPTP; suprathreshold; L-Dopa; -20mg/kg; chronic injections; tolerance; NMDA antagonists; MK-801; CGP; 40116; reinstatement; synergism; parkinsonism;
D O I
10.1007/s007020050158
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Three experiments were performed to study the development and manipulation of tolerance to a suprathreshold dose of L-Dopa (20 mg/kg, s.c.) in MPTP-treated and control (saline-injected) C57 B1/6 mice. The motor activity reinstatement effect of this dose of L-Dopa upon MPTP-treated mouse behaviour deteriorated from the 13th injection (Test Day 8) of L-Dopa onwards and reached basal level (i.e. no stimulatory effects of the drug) by the 16th administration (Test Day 10). Administration of L-Dopa to control mice reduced locomotor and rearing activity throughout the tolerance development period (Test Days 1-12) during the first hour after injection, and then increased locomotor activity during the second hour. The effects of combining either a noncompetitive, MK-801, or a competitive, CGP 40116, glutamate antagonist with L-Dopa, following tolerance development, were assessed in MPTP mice on the 23rd day of L-Dopa administration (Test Day 13). MK-801 (0.1 mg/kg, s.c.) reinstated the locomotory and rearing behaviour induced by L-Dopa; CGP 40116 did so also to a greater extent in the dose range 0.01 to 0.03 mg/kg. These results indicate that MPTP-treated mice continue to offer a useful parkinsonian model also for the examination of different aspects of the "wearing-off'' phenomenon of L-Dopa tolerance and in particular the putative glutamatergic involvement. The clinical consequences may be far-reaching for the utility of L-Dopa in Parkinson's disease, whether the effects demonstrated be of a reinstatement or synergistic nature, once therapeutically adequate glutamate antagonists are more readily available.
引用
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页码:283 / 300
页数:18
相关论文
共 56 条
[1]   CONTROLLED-RELEASE SINEMET (CR-4) - A DOUBLE-BLIND CROSSOVER STUDY IN PATIENTS WITH FLUCTUATING PARKINSONS-DISEASE [J].
AHLSKOG, JE ;
MUENTER, MD ;
MCMANIS, PG ;
BELL, GN ;
BAILEY, PA .
MAYO CLINIC PROCEEDINGS, 1988, 63 (09) :876-886
[2]   CENTRAL NORADRENALINE DEPLETION ANTAGONIZES ASPECTS OF D-AMPHETAMINE-INDUCED HYPERACTIVITY IN THE RAT [J].
ARCHER, T ;
FREDRIKSSON, A ;
JONSSON, G ;
LEWANDER, T ;
MOHAMMED, AK ;
ROSS, SB ;
SODERBERG, U .
PSYCHOPHARMACOLOGY, 1986, 88 (02) :141-146
[3]  
Archer T., 1996, DOPAMINE DIS STATES, P117
[4]  
BARBEAU A, 1969, CAN MED ASSOC J, V101, P791
[5]  
BJORK L, 1991, J PHARMACOL EXP THER, V258, P58
[6]   WEARING-OFF FLUCTUATIONS IN PARKINSONS-DISEASE - CONTRIBUTION OF POSTSYNAPTIC MECHANISMS [J].
BRAVI, D ;
MOURADIAN, MM ;
ROBERTS, JW ;
DAVIS, TL ;
SOHN, YH ;
CHASE, TN .
ANNALS OF NEUROLOGY, 1994, 36 (01) :27-31
[7]   THE NMDA ANTAGONIST MK-801 CAUSES MARKED LOCOMOTOR STIMULATION IN MONOAMINE-DEPLETED MICE [J].
CARLSSON, M ;
CARLSSON, A .
JOURNAL OF NEURAL TRANSMISSION, 1989, 75 (03) :221-226
[8]  
Chase T N, 1988, J Neural Transm Suppl, V27, P3
[9]  
CHASE TN, 1993, NEUROLOGY, V43, P23
[10]   The significance of continuous dopaminergic stimulation in the treatment of Parkinson's disease [J].
Chase, TN .
DRUGS, 1998, 55 (Suppl 1) :1-9