Cortical gamma oscillations are associated with cognitive processes and are
altered in several neuropsychiatric conditions such as schizophrenia and
Alzheimer’s disease. Since dopamine D3 receptors are possible targets in
treatment of these conditions, it is of great importance to understand their
role in modulation of gamma oscillations. The effect of D3 receptors on gamma
oscillations and the underlying cellular mechanisms were investigated by
extracellular local field potential and simultaneous intracellular sharp
micro-electrode recordings in the CA3 region of the hippocampus in vitro. D3
receptors decreased the power and broadened the bandwidth of gamma
oscillations induced by acetylcholine or kainate. Blockade of the D3 receptors
resulted in faster synchronization of the oscillations, suggesting that
endogenous dopamine in the hippocampus slows down the dynamics of gamma
oscillations by activation of D3 receptors. Investigating the underlying
cellular mechanisms for these effects showed that D3 receptor activation
decreased the rate of action potentials (APs) during gamma oscillations and
reduced the precision of the AP phase coupling to the gamma cycle in CA3
pyramidal cells. The results may offer an explanation how selective activation
of D3 receptors may impair cognition and how, in converse, D3 antagonists may
exert pro-cognitive and antipsychotic effects