Diminished catalepsy and dopamine metabolism distinguish aripiprazole from haloperidol or risperidone

被引:38
作者
Nakai, S
Hirose, T
Uwahodo, Y
Imaoka, T
Okazaki, H
Miwa, T
Nakai, M
Yamada, S
Dunn, B
Burris, KD
Molinoff, PB
Tottori, K
Altar, CA
Kikuchi, T
机构
[1] Otsuka Pharmaceut Co Ltd, Inst New Drug Res 2, Tokushima 7710192, Japan
[2] Otsuka Maryland Res Inst, Rockville, MD 20850 USA
[3] Bristol Myers Squibb Co, Pharmaceut Res Inst, Neurosci & Genitourinary Drug Discovery, Wallingford, CT 06492 USA
关键词
aripiprazole; haloperidol; risperidone; catalepsy; dopamine; partial agonist; atypical antipsychotic;
D O I
10.1016/S0014-2999(03)01857-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Catalepsy and changes in striatal and limbic dopamine metabolism were investigated in mice after oral administration of aripiprazole, haloperidol, and risperidone. Catalepsy duration decreased with chronic (21 day) aripiprazole compared with acute (single dose) treatment across a wide dose range, whereas catalepsy duration persisted with chronic haloperidol treatment. At the time of maximal catalepsy, acute aripiprazole did not alter neostriatal dopamine metabolite/dopamine ratios or homovanillic acid (HVA) levels, and produced small increases in dihydroxyphenylacetic acid (DOPAC). Effects were similar in the olfactory tubercle. Dopamine metabolism was essentially unchanged in both regions after chronic aripiprazole. Acute treatments with haloperidol or risperidone elevated DOPAC, HVA, and metabolite/dopamine ratios in both brain areas and these remained elevated with chronic treatment. The subtle effects of aripiprazole on striatal and limbic dopamine metabolism, and the decrease in catalepsy with chronic administration, illustrate fundamental differences in dopamine neurochemical actions and behavioral sequelae of aripiprazole compared to haloperidol or risperidone. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 97
页数:9
相关论文
共 49 条
[1]  
ALTAR CA, 1986, BRAIN RES BULL, V16, P517
[2]  
ALTAR CA, 1988, MOL PHARMACOL, V33, P690
[3]  
ALTAR CA, 1987, EUR J PHARMACOL, V134, P303
[4]   Experimental investigations for the mariculture of Gracilaria in Saldanha Bay, South Africa [J].
Anderson, RJ ;
Levitt, GJ ;
Share, A .
JOURNAL OF APPLIED PHYCOLOGY, 1996, 8 (4-5) :421-430
[5]   Differentiation of classical and novel antipsychotics using animal models [J].
Arnt, J ;
Skarsfeldt, T ;
Hyttel, J .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1997, 12 :S9-S17
[6]   Do novel antipsychotics have similar pharmacological characteristics? A review of the evidence [J].
Arnt, J ;
Skarsfeldt, T .
NEUROPSYCHOPHARMACOLOGY, 1998, 18 (02) :63-101
[7]   TOLERANCE PHENOMENA WITH NEUROLEPTICS CATALEPSY, APOMORPHINE STEREOTYPES AND STRIATAL DOPAMINE METABOLISM IN RAT AFTER SINGLE AND REPEATED ADMINISTRATION OF LOXAPINE AND HALOPERIDOL [J].
ASPER, H ;
BAGGIOLINI, M ;
BURKI, HR ;
LAUENER, H ;
RUCH, W ;
STILLE, G .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1973, 22 (03) :287-294
[8]   SENSITIZATION VERSUS TOLERANCE TO HALOPERIDOL-INDUCED CATALEPSY - MULTIPLE DETERMINANTS [J].
BARNES, DE ;
ROBINSON, B ;
CSERNANSKY, JG ;
BELLOWS, EP .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 36 (04) :883-887
[9]   REGIONAL SELECTIVITY OF NEUROLEPTIC DRUGS - AN ARGUMENT FOR SITE SPECIFICITY [J].
BORISON, RL ;
DIAMOND, BI .
BRAIN RESEARCH BULLETIN, 1983, 11 (02) :215-218
[10]   MODULATION OF INVIVO DOPAMINE RELEASE BY D-2 BUT NOT D-1 RECEPTOR AGONISTS AND ANTAGONISTS [J].
BOYAR, WC ;
ALTAR, CA .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (03) :824-831