cAMP-mediated upregulation of HCN channels in VTA dopamine neurons promotes cocaine reinforcement

Abstract

Abstract Chronic cocaine exposure induces enduring neuroadaptations that facilitate motivated drug taking. Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels are known to modulate neuronal firing and pacemaker activity in ventral tegmental area (VTA) dopamine neurons. However, it remained unknown whether cocaine self-administration affects HCN channel function and whether HCN channel activity modulates motivated drug taking. We report that rat VTA dopamine neurons predominantly express Hcn3-4 mRNA, while VTA GABA neurons express Hcn1–4 mRNA. Both neuronal types display similar hyperpolarization-activated currents (I h ), which are facilitated by acute increases in cAMP. Acute cocaine application decreases voltage-dependent activation of I h in VTA dopamine neurons, but not in GABA neurons. Unexpectedly, chronic cocaine self-administration results in enhanced I h selectively in VTA dopamine neurons. This differential modulation of I h currents is likely mediated by a D 2 autoreceptor-induced decrease in cAMP as D 2 ( Drd2 ) mRNA is predominantly expressed in dopamine neurons, whereas D 1 ( Drd1 ) mRNA is barely detectable in the VTA. Moreover, chronically decreased cAMP via Gi-DREADD stimulation leads to an increase in I h in VTA dopamine neurons and enhanced binding of HCN3/HCN4 with tetratricopeptide repeat-containing Rab8b-interacting protein (TRIP8b), an auxiliary subunit that is known to facilitate HCN channel surface trafficking. Finally, we show that systemic injection and intra-VTA infusion of the HCN blocker ivabradine reduces cocaine self-administration under a progressive ratio schedule and produces a downward shift of the cocaine dose-response curve. Our results suggest that cocaine self-administration induces an upregulation of I h in VTA dopamine neurons, while HCN inhibition reduces the motivation for cocaine intake.