Dopamine Neurons Mediate a Fast Excitatory Signal via Their Glutamatergic Synapses

• DOI: 10.1523/jneurosci.4317-03.2004
• Publication Date: 2004-01-29T03:23:41Z
• Authors: Nao Chuhma; Hui Zhang; Justine Masson; Xiaoxi Zhuang; David Sulzer; René Hen; Stephen Rayport
• Keywords: Male; Neurons; Heterozygote; Motivation; Patch-Clamp Techniques; Receptors, Dopamine D2; Dopamine; Glutamic Acid; Mice, Transgenic; Neural Inhibition; In Vitro Techniques; Nucleus Accumbens; Luminescent Proteins; Mice; 03 medical and health sciences; 0302 clinical medicine; Bacterial Proteins; Genes, Reporter; Dopamine Agonists; Synapses; Animals; Female

Dopamine neurons are thought to convey a fast, incentive salience signal, faster than can be mediated by dopamine. A resolution of this paradox may be that midbrain dopamine neurons exert fast excitatory actions. Using transgenic mice with fluorescent dopamine neurons, in which the axonal projections of the neurons are visible, we made horizontal brain slices encompassing the mesoaccumbens dopamine projection. Focal extracellular stimulation of dopamine neurons in the ventral tegmental area evoked dopamine release and early monosynaptic and late polysynaptic excitatory responses in postsynaptic nucleus accumbens neurons. Local superfusion of the ventral tegmental area with glutamate, which should activate dopamine neurons selectively, produced an increase in excitatory synaptic events. Local superfusion of the ventral tegmental area with the D2 agonist quinpirole, which should increase the threshold for dopamine neuron activation, inhibited the early response. So dopamine neurons make glutamatergic synaptic connections to accumbens neurons. We propose that dopamine neuron glutamatergic transmission may be the initial component of the incentive salience signal.