Cellular perspectives on the glutamate-monoamine interactions in limbic lobe structures and their relevance for some psychiatric disorders

被引:77
作者
Pralong, E
Magistretti, P
Stoop, R
机构
[1] Univ Lausanne, Inst Biol Cellulaire & Morphol, CH-1005 Lausanne, Switzerland
[2] Univ Lausanne, Inst Physiol, CH-1005 Lausanne, Switzerland
关键词
D O I
10.1016/S0301-0082(02)00017-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dopaminergic, serotonergic and noradrenergic nuclei form the trimonoamine modulating system (TMMS). This system modulates emotional/motivational activities mediated by the limbic circuitry, where glutamate is the major excitatory neurotransmitter. Two main concepts are the basis of this review. First, since 1950 and the discovery of the antipsychotic activity of the dopamine D2 receptor antagonist chlorpromazine, it appears that drugs that can modulate the TMMS possess therapeutic psychiatric properties. Second, the concept of glutamate/trimonoamine imbalance in the cortico-striato-thalamo-cortical loop that has been so successful in explaining the pathophysiology of Parkinson disease has been applied in the pathophysiology of schizophrenia. This review will focus on the complex interactions between the fast synaptic glutamatergic transmission and the TMMS in specific parts of the limbic lobe and we will try to link these interactions to some psychiatric disorders, mainly depression, schizophrenia and drug addiction. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:173 / 202
页数:30
相关论文
共 395 条
[1]   D1 dopamine receptor activation reduces extracellular glutamate and GABA concentrations in the medial prefrontal cortex [J].
Abekawa, T ;
Ohmori, T ;
Ito, K ;
Koyama, T .
BRAIN RESEARCH, 2000, 867 (1-2) :250-254
[2]   The NMDA antagonist model for schizophrenia: Promise and pitfalls [J].
Abi-Saab, WM ;
D'Souza, DC ;
Moghaddam, B ;
Krystal, JH .
PHARMACOPSYCHIATRY, 1998, 31 :104-109
[3]   Delayed onset of enhanced MK-801-induced motor hyperactivity after neonatal lesions of the rat ventral hippocampus [J].
Al-Amin, HA ;
Weickert, CS ;
Weinberger, DR ;
Lipska, BK .
BIOLOGICAL PSYCHIATRY, 2001, 49 (06) :528-539
[4]  
ALEXANDER GE, 1990, PROG BRAIN RES, V85, P119
[5]   FACILITATION OF NEOCORTICAL KINDLING BY DEPLETION OF FOREBRAIN NORADRENALINE [J].
ALTMAN, IM ;
CORCORAN, ME .
BRAIN RESEARCH, 1983, 270 (01) :174-177
[6]   Effect of catecholamine depletion on lithium-induced long-term remission of bipolar disorder [J].
Anand, A ;
Darnell, A ;
Miller, HL ;
Berman, RM ;
Cappiello, A ;
Oren, DA ;
Woods, SW ;
Charney, DS .
BIOLOGICAL PSYCHIATRY, 1999, 45 (08) :972-978
[7]   PHARMACOLOGICALLY DISTINCT ACTIONS OF SEROTONIN ON SINGLE PYRAMIDAL NEURONS OF THE RAT HIPPOCAMPUS RECORDED INVITRO [J].
ANDRADE, R ;
NICOLL, RA .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 394 :99-124
[8]   A-G PROTEIN COUPLES SEROTONIN AND GABA-B RECEPTORS TO THE SAME CHANNELS IN HIPPOCAMPUS [J].
ANDRADE, R ;
MALENKA, RC ;
NICOLL, RA .
SCIENCE, 1986, 234 (4781) :1261-1265
[9]   Acceleration of the effect of selected antidepressant drugs in major depression by 5-HT1A antagonists [J].
Artigas, F ;
Romero, L ;
deMontigny, C ;
Blier, P .
TRENDS IN NEUROSCIENCES, 1996, 19 (09) :378-383
[10]  
ASSAF SY, 1979, J PHYSIOL-LONDON, V292, pP52