Heterosynaptic dopamine neurotransmission selects sets of corticostriatal terminals

被引:283
作者
Bamford, NS
Zhang, H
Schmitz, Y
Wu, NP
Cepeda, C
Levine, MS
Schmauss, C
Zakharenko, SS
Zablow, L
Sulzer, D [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Neurol, New York, NY 10032 USA
[2] Univ Washington, Childrens Hosp & Reg Med Ctr, Dept Neurol, Dept Pediat, Seattle, WA 98105 USA
[3] Columbia Univ, Coll Phys & Surg, Dept Psychiat, New York, NY 10032 USA
[4] Columbia Univ, Coll Phys & Surg, Ctr Neurobiol & Behav, Howard Hughes Med Inst, New York, NY 10032 USA
[5] Univ Calif Los Angeles, Mental Retardat Res Ctr, David Geffen Sch Med, Los Angeles, CA 90095 USA
[6] New York State Psychiat Inst & Hosp, Dept Neurosci, New York, NY 10032 USA
关键词
D O I
10.1016/S0896-6273(04)00265-X
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Dopamine input to the striatum is required for voluntary motor movement, behavioral reinforcement, and responses to drugs of abuse. It is speculated that these functions are dependent on either excitatory or inhibitory modulation of corticostriatal synapses onto medium spiny neurons (MSNs). While dopamine modulates MSN excitability, a direct presynaptic effect on the corticostriatal input has not been clearly demonstrated. We combined optical monitoring of synaptic vesicle exocytosis from motor area corticostriatal afferents and electrochemical recordings of striatal dopamine release to directly measure effects of dopamine at the level of individual presynaptic terminals. Dopamine released by either electrical stimulation or amphetamine acted via D2 receptors to inhibit the activity of subsets of corticostriatal terminals. Optical and electrophysiological data suggest that heterosynaptic inhibition was enhanced by higher frequency stimulation and was selective for the least active terminals. Thus, dopamine, by filtering less active inputs, appears to reinforce specific sets of corticostriatal synaptic connections.
引用
收藏
页码:653 / 663
页数:11
相关论文
共 41 条
[1]
OPTICAL ANALYSIS OF SYNAPTIC VESICLE RECYCLING AT THE FROG NEUROMUSCULAR-JUNCTION [J].
BETZ, WJ ;
BEWICK, GS .
SCIENCE, 1992, 255 (5041) :200-203
[2]
Brager DH, 2003, J NEUROSCI, V23, P10475
[3]
Ultrastructural localization of D1 dopamine receptor immunoreactivity in rat striatonigral neurons and its relation with dopaminergic innervation [J].
Caille, I ;
Dumartin, B ;
Bloch, B .
BRAIN RESEARCH, 1996, 730 (1-2) :17-31
[4]
CALABRESI P, 1993, BRAIN, V116, P433
[5]
Calabresi P, 1997, J NEUROSCI, V17, P4536
[6]
Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice [J].
Cepeda, C ;
Hurst, RS ;
Altemus, KL ;
Flores-Hernández, J ;
Calvert, CR ;
Jokel, ES ;
Grandy, DK ;
Low, MJ ;
Rubinstein, M ;
Ariano, MA ;
Levine, MS .
JOURNAL OF NEUROPHYSIOLOGY, 2001, 85 (02) :659-670
[7]
D-2 DOPAMINE-RECEPTOR PROTEIN LOCATION - GOLGI IMPREGNATION-GOLD TONED AND ULTRASTRUCTURAL ANALYSIS OF THE RAT NEOSTRIATUM [J].
FISHER, RS ;
LEVINE, MS ;
SIBLEY, DR ;
ARIANO, MA .
JOURNAL OF NEUROSCIENCE RESEARCH, 1994, 38 (05) :551-564
[8]
FloresHernandez J, 1997, SYNAPSE, V25, P185, DOI 10.1002/(SICI)1098-2396(199702)25:2<185::AID-SYN9>3.0.CO
[9]
2-8
[10]
TERMINAL EXCITABILITY OF THE CORTICOSTRIATAL PATHWAY .1. REGULATION BY DOPAMINE RECEPTOR STIMULATION [J].
GARCIAMUNOZ, M ;
YOUNG, SJ ;
GROVES, PM .
BRAIN RESEARCH, 1991, 551 (1-2) :195-206