Serotonin-GABA interactions modulate MDMA-induced mesolimbic dopamine release

被引:61
作者
Bankson, MG [1 ]
Yamamoto, BK [1 ]
机构
[1] Boston Univ, Sch Med, Dept Pharmacol & Expt Therapeut, Neurochem Lab, Boston, MA 02118 USA
关键词
dopamine; gamma amino butyric acid; 3,4-methylenedioxymethamphetamine; nucleus accumbens; serotonin; ventral tegmental area;
D O I
10.1111/j.1471-4159.2004.02763.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
3,4,-Methylenedioxymethamphetamine (MDMA; 'ecstasy') acts at monoamine nerve terminals to alter the release and re-uptake of dopamine and 5-HT. The present study used microdialysis in awake rats to measure MDMA-induced changes in extracellular GABA in the ventral tegmental area (VTA), simultaneous with measures of extracellular dopamine (DA) in the nucleus accumbens (NAC) shell. (+)-MDMA (0, 2.5, 5 and 10 mg/kg, i.p.) increased GABA efflux in the VTA with a bell-shaped dose-response. This increase was blocked by application of TTX through the VTA probe. MDMA (5 mg/kg) increased 5-HT efflux in VTA by 1037% (p < 0.05). The local perfusion of the 5-HT2B/2C antagonist SB 206553 into the VTA reduced VTA GABA efflux after MDMA from a maximum of 229% to a maximum of 126% of basal values (p < 0.05), while having no effect on basal extracellular GABA concentrations. DA concentrations measured simultaneously in the NAC shell were increased from a maximum of 486% to 1320% (p < 0.05). The selective DA releaser d-amphetamine (AMPH) (4 mg/kg) also increased VTA GABA efflux (180%), did not alter 5-HT and increased NAC DA (875%) (p < 0.05), but the perfusion of SB 206553 into the VTA failed to alter these effects. These results suggest that MDMA-mediated increases in DA within the NAC shell are dampened by increases in VTA GABA subsequent to activation of 5-HT2B/2C receptors in the VTA.
引用
收藏
页码:852 / 859
页数:8
相关论文
共 56 条
[1]   Pharmacological studies of the acute effects of (+)-3,4-methylenedioxymethamphetamine on locomotor activity:: Role of 5-HT1B/1D and 5-HT2 receptors [J].
Bankson, MG ;
Cunningham, KA .
NEUROPSYCHOPHARMACOLOGY, 2002, 26 (01) :40-52
[2]   A review of central 5-HT receptors and their function [J].
Barnes, NM ;
Sharp, T .
NEUROPHARMACOLOGY, 1999, 38 (08) :1083-1152
[3]  
Berg KA, 2001, J PHARMACOL EXP THER, V299, P593
[4]   COMPARISON OF EFFECTS OF L-DOPA, AMPHETAMINE AND APOMORPHINE ON FIRING RATE OF RAT DOPAMINERGIC NEURONS [J].
BUNNEY, BS ;
AGHAJANIAN, GK ;
ROTH, RH .
NATURE-NEW BIOLOGY, 1973, 245 (143) :123-125
[5]  
CALLAWAY CW, 1992, NEUROPSYCHOPHARMACOL, V7, P113
[6]   DOPAMINE D1 RECEPTORS FACILITATE TRANSMITTER RELEASE [J].
CAMERON, DL ;
WILLIAMS, JT .
NATURE, 1993, 366 (6453) :344-347
[7]   OPPOSING ROLES FOR DOPAMINE AND SEROTONIN AT PRESYNAPTIC RECEPTORS IN THE VENTRAL TEGMENTAL AREA [J].
CAMERON, DL ;
WILLIAMS, JT .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1995, 22 (11) :841-845
[8]  
De Deurwaerdère P, 1998, J NEUROSCI, V18, P6528
[9]  
Di Giovanni G, 2000, SYNAPSE, V35, P53, DOI 10.1002/(SICI)1098-2396(200001)35:1<53::AID-SYN7>3.0.CO
[10]  
2-2