Involvement of serotonin and dopamine in the mechanism of action of novel antidepressant drugs: A review

被引:87
作者
Bonhomme, N [1 ]
Esposito, E [1 ]
机构
[1] Ist Ric Farmacol Mario Negri, Consorzio Mario Negri Sud, I-66030 Santa Maria Imbaro, Italy
关键词
D O I
10.1097/00004714-199812000-00005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Several hypotheses regarding the physiopathology of major depression exist. Attention has been focused on cerebral monoaminergic systems, the dysfunction of which is thought to underlie various aspects of depressive symptomatology. There is extensive literature describing the involvement of serotonergic and dopaminergic systems in the mechanism of action of antidepressant drugs. However, a unitary analysis of the data in terms of interaction between different monoaminergic systems is still lacking. In this article, studies reporting the biochemical, behavioral, and clinical effects of tricyclic antidepressants (TCAs), monoamine oxidase inhibitors (MAOIs), selective serotonin reuptake inhibitors (SSRIs), selective blockers of presynaptic dopamine (DA) receptors, and antagonists of serotonin-2 (5-hydroxytryptamine-2 [5-HT2]) receptors were reviewed. Analysis of the current literature indicates that long-term treatment with antidepressants causes adaptive changes of the serotonergic and dopaminergic systems. In particular, long-term administration of TCAs enhances the responsiveness of postsynaptic serotonin receptors to iontophoretically applied serotonin and potentiates the behavioral responses to both direct and indirect dopaminergic agonists. Repeated administration of SSRIs and MAOIs increases serotonergic transmission by desensitizing the inhibitory 5-HT1A somatodendritic and terminal 5-HT1B/1D antoreceptors. Selective blockers of DA autoreceptors exert their antidepressant effect by enhancing DA release. A similar mechanism of action could be hypothesized for HT2 receptor antagonists. There is general agreement that the clinical effect of antidepressant drugs, which becomes evident only after long-term treatment, is caused by their ability to induce adaptive changes of the monoaminergic systems. Increases in both serotonergic and dopaminergic function have been consistently found after longterm treatment with Various classes of antidepressant drugs. Recent studies have focused on the functional interaction between the serotonergic and dopaminergic systems to explain the mechanism of the antidepressant action of SSRIs and 5-HT2 antagonists.
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页码:447 / 454
页数:8
相关论文
共 103 条
[31]   CONTROLLED RANDOMIZED GROUP COMPARISON OF NOMIFENSINE AND IMIPRAMINE IN DEPRESSIVE-ILLNESS [J].
FORREST, A ;
HEWETT, A ;
NICHOLSON, P .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1977, 4 :S215-S220
[32]   MOTOR EFFECTS OF SEROTONIN IN THE CENTRAL NERVOUS-SYSTEM [J].
GERSON, SC ;
BALDESSARINI, RJ .
LIFE SCIENCES, 1980, 27 (16) :1435-1451
[33]  
GLASER T, 1988, Drugs of the Future, V13, P429
[34]   5-HT1A PARTIAL AGONISTS - WHAT IS THEIR FUTURE [J].
GLITZ, DA ;
POHL, R .
DRUGS, 1991, 41 (01) :11-18
[35]  
GOLDEN RN, 1988, ARCH GEN PSYCHIAT, V45, P139
[36]   DOPAMINERGIC AGONIST NOMIFENSINE COMPARED WITH AMITRIPTYLINE - DOUBLE-BLIND CLINICAL-TRIAL IN ACUTE PRIMARY DEPRESSIONS [J].
GROF, P ;
SAXENA, B ;
DAIGLE, L ;
MAHUTTE, G .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1977, 4 :S221-S225
[37]   POTENTIATION BY LOW-DOSES OF SELECTED NEUROLEPTICS OF FOOD-INDUCED CONDITIONED PLACE PREFERENCE IN RATS [J].
GUYON, A ;
ASSOULYBESSE, F ;
BIALA, G ;
PUECH, AJ ;
THIEBOT, MH .
PSYCHOPHARMACOLOGY, 1993, 110 (04) :460-466
[38]  
Hammer RP, 1993, DEPRESSION, V1, P82
[39]   SEROTONIN AXON TERMINALS IN THE VENTRAL TEGMENTAL AREA OF THE RAT - FINE-STRUCTURE AND SYNAPTIC INPUT TO DOPAMINERGIC-NEURONS [J].
HERVE, D ;
PICKEL, VM ;
JOH, TH ;
BEAUDET, A .
BRAIN RESEARCH, 1987, 435 (1-2) :71-83
[40]   SEROTONIN 5-HT1A AUTORECEPTOR BLOCKADE POTENTIATES THE ABILITY OF THE 5-HT REUPTAKE INHIBITOR CITALOPRAM TO INCREASE NERVE-TERMINAL OUTPUT OF 5-HT INVIVO - A MICRODIALYSIS STUDY [J].
HJORTH, S .
JOURNAL OF NEUROCHEMISTRY, 1993, 60 (02) :776-779