D2-Like Dopamine Receptors Modulate SKCaChannel Function in Subthalamic Nucleus Neurons Through Inhibition of Cav2.2 Channels

Abstract

The activity patterns of subthalamic nucleus (STN) neurons are intimately related to motor function/dysfunction and modulated directly by dopaminergic neurons that degenerate in Parkinson's disease (PD). To understand how dopamine and dopamine depletion influence the activity of the STN, the functions/signaling pathways/substrates of D2-like dopamine receptors were studied using patch-clamp recording. In rat brain slices, D2-like dopamine receptor activation depolarized STN neurons, increased the frequency/irregularity of their autonomous activity, and linearized/enhanced their firing in response to current injection. Activation of D2-like receptors in acutely isolated neurons reduced transient outward currents evoked by suprathreshold voltage steps. Modulation was inhibited by a D2-like receptor antagonist and occluded by voltage-dependent Ca2+(Cav) channel or small-conductance Ca2+-dependent K+(SKCa) channel blockers or Ca2+-free media. Because Cavchannels are targets of Gi/o-linked receptors, actions on step- and action potential waveform-evoked Cavchannel currents were studied. D2-like receptor activation reduced the conductance of Cav2.2 but not Cav1 channels. Modulation was mediated, in part, by direct binding of Gβγ subunits because it was attenuated by brief depolarization. D2and/or D3dopamine receptors may mediate modulation because a D4-selective agonist was ineffective and mRNA encoding D2and D3but not D4dopamine receptors was detectable. Brain slice recordings confirmed that SKCachannel-mediated action potential afterhyperpolarization was attenuated by D2-like dopamine receptor activation. Together, these data suggest that D2-like dopamine receptors potently modulate the negative feedback control of firing that is mediated by the functional coupling of Cav2.2 and SKCachannels in STN neurons.