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Dopamine neuron dependent behaviors mediated by glutamate cotransmission.

eLife | 2017

Dopamine neurons in the ventral tegmental area use glutamate as a cotransmitter. To elucidate the behavioral role of the cotransmission, we targeted the glutamate-recycling enzyme glutaminase (gene Gls1). In mice with a dopamine transporter (Slc6a3)-driven conditional heterozygous (cHET) reduction of Gls1 in their dopamine neurons, dopamine neuron survival and transmission were unaffected, while glutamate cotransmission at phasic firing frequencies was reduced, enabling a selective focus on the cotransmission. The mice showed normal emotional and motor behaviors, and an unaffected response to acute amphetamine. Strikingly, amphetamine sensitization was reduced and latent inhibition potentiated. These behavioral effects, also seen in global GLS1 HETs with a schizophrenia resilience phenotype, were not seen in mice with an Emx1-driven forebrain reduction affecting most brain glutamatergic neurons. Thus, a reduction in dopamine neuron glutamate cotransmission appears to mediate significant components of the GLS1 HET schizophrenia resilience phenotype, and glutamate cotransmission appears to be important in attribution of motivational salience.

Pubmed ID: 28703706 RIS Download

Associated grants

  • Agency: NIMH NIH HHS, United States
    Id: R01 MH087758
  • Agency: NIMH NIH HHS, United States
    Id: P50 MH086404
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA017978
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH117128
  • Agency: NIDA NIH HHS, United States
    Id: P01 DA010154
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA038966
  • Agency: NCI NIH HHS, United States
    Id: P30 CA013696

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