EFFECT OF NONDOPAMINERGIC DRUGS ON L-DOPA-INDUCED DYSKINESIAS IN MPTP-TREATED MONKEYS

被引:172
作者
GOMEZMANCILLA, B
BEDARD, PJ
机构
[1] HOP ENFANTS JESUS,CTR RECH NEUROBIOL,1401 18E RUE,QUEBEC CITY G1J 1Z4,PQ,CANADA
[2] UNIV LAVAL,FAC MED,DEPT PHARMACOL,QUEBEC CITY G1K 7P4,QUEBEC,CANADA
关键词
L-DOPA; MPTP-INDUCED PARKINSONISM; DYSKINESIA; NONDOPAMINERGIC DRUG THERAPY;
D O I
10.1097/00002826-199310000-00004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A group of four monkeys was rendered parkinsonian with the toxin MPTP. They were then treated chronically with L-DOPA/benserazide 50/12.5 mg/kg given orally daily for 2 months. This dose produced a striking antiparkinsonian effect, but all animals manifested dyskinesia. A series of agents acting primarily on neurotransmitters other than dopamine were then tested in combination with L-DOPA to see if the dyskinetic movements would be modified. Several drugs, including clonidine, physostigmine, methysergide, 5-MDOT, propranolol, and MK-801, markedly reduced the dyskinetic movements but at the cost of a return of parkinsonian symptomatology. However, yohimbine and meperidine reduced predominantly the dyskinetic movements. Baclofen was also useful in one monkey against a more dystonic form of dyskinesia. Atropine converted the dystonic movements into chorea.
引用
收藏
页码:418 / 427
页数:10
相关论文
共 50 条
[1]  
BEDARD PJ, 1986, BRAIN RES, P379
[2]   DIFFERENTIAL-EFFECTS OF D1 AND D2 AGONISTS IN MPTP-TREATED PRIMATES - FUNCTIONAL IMPLICATIONS FOR PARKINSONS-DISEASE [J].
BOYCE, S ;
RUPNIAK, NMJ ;
STEVENTON, MJ ;
IVERSEN, SD .
NEUROLOGY, 1990, 40 (06) :927-933
[3]   CHARACTERIZATION OF DYSKINESIAS INDUCED BY L-DOPA IN MPTP-TREATED SQUIRREL-MONKEYS [J].
BOYCE, S ;
RUPNIAK, NMJ ;
STEVENTON, MJ ;
IVERSEN, SD .
PSYCHOPHARMACOLOGY, 1990, 102 (01) :21-27
[4]   A PRIMATE MODEL OF PARKINSONISM - SELECTIVE DESTRUCTION OF DOPAMINERGIC-NEURONS IN THE PARS COMPACTA OF THE SUBSTANTIA NIGRA BY N-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE [J].
BURNS, RS ;
CHIUEH, CC ;
MARKEY, SP ;
EBERT, MH ;
JACOBOWITZ, DM ;
KOPIN, IJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (14) :4546-4550
[5]   THE NONCOMPETITIVE NMDA ANTAGONISTS MK-801 AND PCP, AS WELL AS THE COMPETITIVE NMDA ANTAGONIST SDZ EAA494 (D-CPPENE), INTERACT SYNERGISTICALLY WITH CLONIDINE TO PROMOTE LOCOMOTION IN MONOAMINE-DEPLETED MICE [J].
CARLSSON, M ;
SVENSSON, A .
LIFE SCIENCES, 1990, 47 (19) :1729-1736
[6]  
COHEN DJ, 1980, ARCH GEN PSYCHIAT, V37, P1350
[7]   MPTP-INDUCED PARKINSONISM IN THE MONKEY - NEUROCHEMICAL PATHOLOGY, COMPLICATIONS OF TREATMENT AND PATHOPHYSIOLOGICAL MECHANISMS [J].
CROSSMAN, AR ;
CLARKE, CE ;
BOYCE, S ;
ROBERTSON, RG ;
SAMBROOK, MA .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1987, 14 (03) :428-435
[8]   EFFECT OF THE NMDA ANTAGONIST MK-801 ON MPTP-INDUCED PARKINSONISM IN THE MONKEY [J].
CROSSMAN, AR ;
PEGGS, D ;
BOYCE, S ;
LUQUIN, MR ;
SAMBROOK, MA .
NEUROPHARMACOLOGY, 1989, 28 (11) :1271-1273
[9]  
DIAMOND BI, 1978, NEUROLOGY, V28, P1085
[10]   THE PHYSIOLOGY AND PHARMACOLOGY OF MAMMALIAN BASAL GANGLIA [J].
DRAY, A .
PROGRESS IN NEUROBIOLOGY, 1980, 14 (04) :221-335