Glutamatergic neurons are present in the rat ventral tegmental area

被引:264
作者
Yamaguchi, Tsuyoshi [1 ]
Sheen, Whitney [1 ]
Morales, Marisela [1 ]
机构
[1] Natl Inst Drug Abuse, Baltimore, MD 21224 USA
关键词
dopamine; midbrain; reward; Sprague-Dawley rat; substantia nigra; VGluT2;
D O I
10.1111/j.1460-9568.2006.05263.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ventral tegmental area (VTA) is thought to play an important role in reward function. Two populations of neurons, containing either dopamine (DA) or gamma-amino butyric acid (GABA), have been extensively characterized in this area. However, recent electrophysiological studies are consistent with the notion that neurons that utilize neurotransmitters other than DA or GABA are likely to be present in the VTA. Given the pronounced phenotypic diversity of neurons in this region, we have proposed that additional cell types, such as those that express the neurotransmitter glutamate may also be present in this area. Thus, by using in situ hybridization histochemistry we investigated whether transcripts encoded by genes for the two vesicular glutamate transporters, VGluT1 or VGluT2, were expressed in the VTA. We found that VGluT2 mRNA but not VGluT1 mRNA is expressed in the VTA. Neurons expressing VGluT2 mRNA were differentially distributed throughout the rostro-caudal and medio-lateral aspects of the VTA, with the highest concentration detected in rostro-medial areas. Phenotypic characterization with double in situ hybridization of these neurons indicated that they rarely co-expressed mRNAs for tyrosine hydroxylase (TH, marker for DAergic neurons) or glutamic acid decarboxylase (GAD, marker for GABAergic neurons). Based on the results described here, we concluded that the VTA contains glutamatergic neurons that in their vast majority are clearly non-DAergic and non-GABAergic.
引用
收藏
页码:106 / 118
页数:13
相关论文
共 51 条
[1]   Molecular and functional analysis of a novel neuronal vesicular glutamate transporter [J].
Bai, LQ ;
Xu, H ;
Collins, JF ;
Ghishan, FK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (39) :36764-36769
[2]  
Bellocchio EE, 1998, J NEUROSCI, V18, P8648
[3]   Uptake of glutamate into synaptic vesicles by an inorganic phosphate transporter [J].
Bellocchio, EE ;
Reimer, RJ ;
Fremeau, RT ;
Edwards, RH .
SCIENCE, 2000, 289 (5481) :957-960
[4]   GDNF enhances the synaptic efficacy of dopaminergic neurons in culture [J].
Bourque, MJ ;
Trudeau, LE .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (09) :3172-3180
[5]   A subset of ventral tegmental area neurons is inhibited by dopamine, 5-hydroxytryptamine and opioids [J].
Cameron, DL ;
Wessendorf, MW ;
Williams, JT .
NEUROSCIENCE, 1997, 77 (01) :155-166
[6]  
Carr DB, 2000, SYNAPSE, V38, P114, DOI 10.1002/1098-2396(200011)38:2<114::AID-SYN2>3.0.CO
[7]  
2-R
[9]   D2 receptors inhibit the secretory process downstream from calcium influx in dopaminergic neurons:: Implication of K+ channels [J].
Congar, P ;
Bergevin, A ;
Trudeau, LE .
JOURNAL OF NEUROPHYSIOLOGY, 2002, 87 (02) :1046-1056
[10]   Dopamine neurons in culture express VGLUT2 explaining their capacity to release glutamate at synapses in addition to dopamine [J].
Dal Bo, G ;
St-Gelais, F ;
Danik, M ;
Williams, S ;
Cotton, M ;
Trudeau, LE .
JOURNAL OF NEUROCHEMISTRY, 2004, 88 (06) :1398-1405