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The Journal of Neuroscience, May 1, 2002, 22(9):3404-3413
Selective Coupling of T-Type Calcium Channels to SK Potassium
Channels Prevents Intrinsic Bursting in Dopaminergic Midbrain
Neurons
Jakob
Wolfart and
Jochen
Roeper
Medical Research Council, Anatomical Neuropharmacology Unit,
Department of Pharmacology, Oxford University, Oxford OX1 3TH, United
Kingdom
Dopaminergic midbrain (DA) neurons display two principal activity
patterns in vivo, single-spike and burst firing, the
latter coding for reward-related events. We have shown recently
that the small-conductance calcium-activated potassium channel SK3 controls pacemaker frequency and precision in DA neurons of the substantia nigra (SN), and previous studies have implicated SK channels
in the transition to burst firing. To identify the upstream calcium
sources for SK channel activation in DA SN neurons, we studied the
sensitivity of SK channel-mediated afterhyperpolarization (AHP)
currents to inhibitors of different types of voltage-gated calcium
channels in perforated patch-clamp recordings. Cobalt-sensitive AHP
currents were not affected by L-type and P/Q-type calcium channel
inhibitors and were reduced slightly (26%) by the N-type channel
inhibitor -conotoxin-GVIA. In contrast, AHP currents were blocked
substantially (85-94%) by micromolar concentrations of nickel
(IC50, 33.75 µM) and mibefradil
(IC50, 4.83 µM), indistinguishable from the nickel and mibefradil sensitivities of T-type calcium currents
(IC50 values, 33.86 and 4.59 µM,
respectively). These results indicate that SK channels are activated
selectively via T-type calcium channels in DA SN neurons. Consequently,
SK currents displayed use-dependent inactivation with similar time
constants when compared with those of T-type calcium currents and
generated a transient rebound inhibition. Both SK and T-type channels
were essential for the stability of spontaneous pacemaker activity, and, in some DA SN neurons, T-type channel inhibition was sufficient to
induce intrinsic burst firing. The functional coupling of SK to T-type
channels has important implications for the temporal integration of
synaptic input and might help to understand how DA neurons switch
between pacemaker and burst-firing modes in vivo.
Key words:
dopamine; substantia nigra (A9); electrophysiology; apamin; nifedipine; agatoxin-TK; FTX-3.3; amphotericin; cyclopiazonic
acid (CPA)
Copyright © 2002 Society for Neuroscience 0270-6474/02/2293404-10$05.00/0
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