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A glutamatergic reward input from the dorsal raphe to ventral tegmental area dopamine neurons

Author

Listed:
  • Jia Qi

    (National Institute on Drug Abuse, Neuronal Networks Section, National Institutes of Health)

  • Shiliang Zhang

    (National Institute on Drug Abuse, Neuronal Networks Section, National Institutes of Health)

  • Hui-Ling Wang

    (National Institute on Drug Abuse, Neuronal Networks Section, National Institutes of Health)

  • Huikun Wang

    (National Institute on Drug Abuse, Electrophysiology Research Section, National Institutes of Health)

  • Jose de Jesus Aceves Buendia

    (National Institute on Drug Abuse, Neuronal Networks Section, National Institutes of Health)

  • Alexander F. Hoffman

    (National Institute on Drug Abuse, Electrophysiology Research Section, National Institutes of Health)

  • Carl R. Lupica

    (National Institute on Drug Abuse, Electrophysiology Research Section, National Institutes of Health)

  • Rebecca P. Seal

    (University of Pittsburgh)

  • Marisela Morales

    (National Institute on Drug Abuse, Neuronal Networks Section, National Institutes of Health)

Abstract

Electrical stimulation of the dorsal raphe (DR) and ventral tegmental area (VTA) activates the fibres of the same reward pathway but the phenotype of this pathway and the direction of the reward-relevant fibres have not been determined. Here we report rewarding effects following activation of a DR-originating pathway consisting of vesicular glutamate transporter 3 (VGluT3) containing neurons that form asymmetric synapses onto VTA dopamine neurons that project to nucleus accumbens. Optogenetic VTA activation of this projection elicits AMPA-mediated synaptic excitatory currents in VTA mesoaccumbens dopaminergic neurons and causes dopamine release in nucleus accumbens. Activation also reinforces instrumental behaviour and establishes conditioned place preferences. These findings indicate that the DR–VGluT3 pathway to VTA utilizes glutamate as a neurotransmitter and is a substrate linking the DR—one of the most sensitive reward sites in the brain—to VTA dopaminergic neurons.

Suggested Citation

  • Jia Qi & Shiliang Zhang & Hui-Ling Wang & Huikun Wang & Jose de Jesus Aceves Buendia & Alexander F. Hoffman & Carl R. Lupica & Rebecca P. Seal & Marisela Morales, 2014. "A glutamatergic reward input from the dorsal raphe to ventral tegmental area dopamine neurons," Nature Communications, Nature, vol. 5(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6390
    DOI: 10.1038/ncomms6390
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    Cited by:

    1. Aki Takahashi & Romain Durand-de Cuttoli & Meghan E. Flanigan & Emi Hasegawa & Tomomi Tsunematsu & Hossein Aleyasin & Yoan Cherasse & Ken Miya & Takuya Okada & Kazuko Keino-Masu & Koshiro Mitsui & Lon, 2022. "Lateral habenula glutamatergic neurons projecting to the dorsal raphe nucleus promote aggressive arousal in mice," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
    2. Xin-Yue Wang & Wen-Bin Jia & Xiang Xu & Rui Chen & Liang-Biao Wang & Xiao-Jing Su & Peng-Fei Xu & Xiao-Qing Liu & Jie Wen & Xiao-Yuan Song & Yuan-Yuan Liu & Zhi Zhang & Xin-Feng Liu & Yan Zhang, 2023. "A glutamatergic DRN–VTA pathway modulates neuropathic pain and comorbid anhedonia-like behavior in mice," Nature Communications, Nature, vol. 14(1), pages 1-15, December.

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