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Dopamine neurons projecting to medial shell of the nucleus accumbens drive heroin reinforcement.

Julie Corre | Ruud van Zessen | Michaël Loureiro | Tommaso Patriarchi | Lin Tian | Vincent Pascoli | Christian Lüscher
eLife | 2018

The dopamine (DA) hypothesis posits the increase of mesolimbic dopamine levels as a defining commonality of addictive drugs, initially causing reinforcement, eventually leading to compulsive consumption. While much experimental evidence from psychostimulants supports this hypothesis, it has been challenged for opioid reinforcement. Here, we monitor genetically encoded DA and calcium indicators as well as cFos in mice to reveal that heroin activates DA neurons located in the medial part of the VTA, preferentially projecting to the medial shell of the nucleus accumbens (NAc). Chemogenetic and optogenetic manipulations of VTA DA or GABA neurons establish a causal link to heroin reinforcement. Inhibition of DA neurons blocked heroin self-administration, while heroin inhibited optogenetic self-stimulation of DA neurons. Likewise, heroin occluded the self-inhibition of VTA GABA neurons. Together, these experiments support a model of disinhibition of a subset of VTA DA neurons in opioid reinforcement.

Pubmed ID: 30373717

Associated grants

  • Agency: European Commission, International
    Id: MeSSI
  • Agency: NINDS NIH HHS, United States
    Id: U01 NS090604
  • Agency: NINDS NIH HHS, United States
    Id: U01 NS103522
  • Agency: NIMH NIH HHS, United States
    Id: DP2 MH107056
  • Agency: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, International
    Id: 310030B_170266
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA034388

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