Blockade of dopamine D3 receptors improves hippocampal synaptic function and rescues age‐related cognitive phenotype

Dopamine D3 receptors (D3Rs) modulate neuronal activity in several brain regions including the hippocampus. Although previous studies reported that blocking D3Rs exerts pro‐cognitive effects, their involvement in hippocampal synaptic function and memory in the healthy and aged brain has not been thoroughly investigated. We demonstrated that in adult wild type (WT) mice, D3R pharmacological blockade or genetic deletion as in D3 knock out (KO) mice, converted the weak form of long‐term potentiation (LTP1) into the stronger long‐lasting LTP (LTP2) via the cAMP/PKA pathway, and allowed the formation of long‐term memory. D3R effects were mainly mediated by post‐synaptic mechanisms as their blockade enhanced basal synaptic transmission (BST), AMPAR‐mediated currents, mEPSC amplitude, and the expression of the post‐synaptic proteins PSD‐95, phospho(p)GluA1 and p‐CREB. Consistently, electron microscopy revealed a prevalent expression of D3Rs in post‐synaptic dendrites. Interestingly, with age, D3Rs decreased in axon terminals while maintaining their levels in post‐synaptic dendrites. Indeed, in aged WT mice, blocking D3Rs reversed the impairment of LTP, BST, memory, post‐synaptic protein expression, and PSD length. Notably, aged D3‐KO mice did not exhibit synaptic and memory deficits. In conclusion, we demonstrated the fundamental role of D3Rs in hippocampal synaptic function and memory, and their potential as a therapeutic target to counteract the age‐related hippocampal cognitive decline. Dopamine D3 receptors (D3Rs) blockade acts through the cAMP/PKA pathway leading to long‐lasting LTP and memory. D3Rs are mainly located in post‐synaptic dendrites and their blockade enhances basal synaptic transmission, AMPAR‐mediated currents, mEPSC amplitude, and the expression of PSD‐95, pGluA1, pCREB. In aged mice, D3R blockade reversed synaptic transmission and plasticity, post‐synaptic protein expression, and PSD length. Aged D3‐KO mice did not exhibit synaptic and memory deficits.