Effects of arousal- and feeding-related neuropeptides on dopaminergic and GABAergic neurons in the ventral tegmental area of the rat

被引:137
作者
Korotkova, T. M. [1 ]
Brown, R. E. [1 ]
Sergeeva, O. A. [1 ]
Ponomarenko, A. A. [1 ]
Haas, H. L. [1 ]
机构
[1] Univ Dusseldorf, Inst Neurophysiol, D-40001 Dusseldorf, Germany
关键词
CART; CRF; NPY; reward; substance P;
D O I
10.1111/j.1460-9568.2006.04792.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Many neuropeptides regulate feeding and arousal; the ventral tegmental area (VTA) is likely to be one site where they act. We used whole-cell patch-clamp and single-unit extracellular recordings to examine the effects of such neuropeptides on the activity of VTA neurons. Substance P (SP; 300 nM) increased the firing rate of the majority of VTA dopaminergic and gamma-aminobutyric acid (GABA)ergic neurons, and induced oscillations in two dopaminergic cells. Corticotropin-releasing factor (CRF; 200 nM) excited the majority of VTA cells directly, whereas neuropeptide Y (NPY; 300 nM) directly inhibited a subset of dopaminergic and GABAergic cells. Consecutive application of several neuropeptides revealed that all the neurons were excited by at least one of the excitatory neuropeptides SP, CRF or/and orexins. alpha-Melanocyte-stimulating hormone had no effect on dopaminergic cells (at concentrations of 500 nM and 1 mu M) and affected only a small proportion of GABAergic neurons. Ghrelin (500 nM), agouti-related peptide (1 mu M); cocaine and amphetamine-related transcript (500 nM) and leptin (500 nM and 1 mu M) did not modulate the firing rate and membrane potential of VTA neurons. Single-cell reverse transcription polymerase chain reaction analysis showed that all NPY receptors were present in VTA neurons, and all but one cell expressed NPY and/or at least one NPY receptor. CRF was expressed in 70% of dopaminergic VTA cells; the expression of CRF receptor 2 was more abundant than that of receptor 1. These findings suggest a link between the ability of neuropeptides to promote arousal and their action on VTA neurons.
引用
收藏
页码:2677 / 2685
页数:9
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