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Brief Communications

Rewarding Effects of Optical Stimulation of Ventral Tegmental Area Glutamatergic Neurons

Hui-Ling Wang, Jia Qi, Shiliang Zhang, Huikun Wang and Marisela Morales
Journal of Neuroscience 2 December 2015, 35 (48) 15948-15954; DOI: https://doi.org/10.1523/JNEUROSCI.3428-15.2015
Hui-Ling Wang
Neuronal Networks Section, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224
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Jia Qi
Neuronal Networks Section, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224
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Shiliang Zhang
Neuronal Networks Section, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224
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Huikun Wang
Neuronal Networks Section, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224
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  • ORCID record for Huikun Wang
Marisela Morales
Neuronal Networks Section, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224
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Abstract

Ventral tegmental area (VTA) neurons play roles in reward and aversion. The VTA has three major neuronal phenotypes: dopaminergic, GABAergic, and glutamatergic. VTA glutamatergic neurons—expressing vesicular glutamate transporter-2 (VGluT2)—project to limbic and cortical regions, but also excite neighboring dopaminergic neurons. Here, we test whether local photoactivation of VTA VGluT2 neurons expressing Channelrhodopsin-2 (ChR2) under the VGluT2 promoter causes place preference and supports operant responding for the stimulation. By using a Cre-dependent viral vector, ChR2 (tethered to mCherry) was expressed in VTA glutamatergic neurons of VGluT2::Cre mice. The mCherry distribution was evaluated by immunolabeling. By confocal microscopy, we detected expression of mCherry in VTA cell bodies and local processes. In contrast, VGluT2 expression was restricted to varicosities, some of them coexpressing mCherry. By electron microscopy, we determined that mCherry-VGluT2 varicosities correspond to axon terminals, forming asymmetric synapses on neighboring dopaminergic neurons. These findings indicate that ChR2 was present in terminals containing glutamatergic synaptic vesicles and involved in local synaptic connections. Photoactivation of VTA slices from ChR2-expressing mice induced AMPA/NMDA receptor-dependent firing of dopaminergic neurons projecting to the nucleus accumbens. VTA photoactivation of ChR2-expressing mice reinforced instrumental behavior and established place preferences. VTA injections of AMPA or NMDA receptor antagonists blocked optical self-stimulation and place preference. These findings suggest a role in reward function for VTA glutamatergic neurons through local excitatory synapses on mesoaccumbens dopaminergic neurons.

SIGNIFICANCE STATEMENT We show that previously discovered glutamatergic neurons within the ventral tegmental area (VTA), through their local connections, play a role in reward. The participation of VTA glutamatergic neurons in reward involves VTA glutamatergic neurons that establish local excitatory connections. These neurons concentrate the protein VGluT2 in their axon terminals to transport and accumulate glutamate into vesicles for its synaptic release. The VTA activation of these terminals is rewarding and involves local synaptic glutamate release, which in turn activates glutamatergic receptors in neighboring mesoaccumbens dopaminergic neurons.

  • addiction
  • aversion
  • dopamine
  • reward
  • VGluT2
  • VTA
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The Journal of Neuroscience: 35 (48)
Journal of Neuroscience
Vol. 35, Issue 48
2 Dec 2015
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Rewarding Effects of Optical Stimulation of Ventral Tegmental Area Glutamatergic Neurons
Hui-Ling Wang, Jia Qi, Shiliang Zhang, Huikun Wang, Marisela Morales
Journal of Neuroscience 2 December 2015, 35 (48) 15948-15954; DOI: 10.1523/JNEUROSCI.3428-15.2015

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Rewarding Effects of Optical Stimulation of Ventral Tegmental Area Glutamatergic Neurons
Hui-Ling Wang, Jia Qi, Shiliang Zhang, Huikun Wang, Marisela Morales
Journal of Neuroscience 2 December 2015, 35 (48) 15948-15954; DOI: 10.1523/JNEUROSCI.3428-15.2015
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Keywords

  • addiction
  • aversion
  • dopamine
  • reward
  • VGLUT2
  • VTA

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