The antipsychotic aripiprazole is a potent, partial agonist at the human 5-HT1A receptor

被引:458
作者
Jordan, S
Koprivica, V
Chen, RY
Tottori, K
Kikuchi, T
Altar, CA
机构
[1] Otsuka Maryland Res Inst, Maryland Res Labs, Dept Neurosci, Rockville, MD 20850 USA
[2] Otsuka Pharmaceut Co Ltd, CNS Res Grp, Res Inst Pharmacol & Therapeut Dev, Tokushima 7710192, Japan
关键词
aripiprazole (OPC-14597); partial agonist; schizophrenia; 5-HT; (5-hydroxytryptomine; seretonin); dopamine;
D O I
10.1016/S0014-2999(02)01532-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aripiprazole, 7-{4-[4-(2,3-dichlorophenyl)-1-piperazinyl]butyloxy}-3,4-dihydro-2(1H)-quinolinone, a novel antipsychotic with partial agonist activity at dopamine D2 receptors, bound with high affinity to recombinant human 5-HT1A receptors (h5-HT1A) in Chinese hamster ovary cell membranes and displayed potent, partial agonism at 5-HT1A receptors in a guanosine-5'-O-(3-[S-35]thio)-triphosphate ([S-35]GTPgammaS)-binding assay that was blocked completely by a selective 5-HT1A receptor antagonist. An interaction with 5-HT1A receptors may contribute to the overall efficacy of aripiprazole against symptoms of schizophrenia. including anxiety, depression, cognitive and negative symptoms, and to its favorable side-effect profile. Combined with previous studies demonstrating the potent partial agonism of aripiprazole at dopamine D2 receptors, this study suggests aripiprazole is the first dopamine-serotonin system stabilizer. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
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页码:137 / 140
页数:4
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