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¹ Northwestern University, Department of Physiology, Feinberg School of Medicine, 303 E. Chicago Avenue, Chicago, IL 60611, USA
² Université de Bordeaux 2, Laboratoire Mouvement Adaptation Cognition, UMR CNRS 5227, 146 Rue Léo Saignat, 33076 Bordeaux Cedex, France

Reciprocally connected glutamatergic subthalamic nucleus (STN) and GABAergic external globus pallidus (GP) neurons normally exhibit weakly correlated, irregular activity but following the depletion of dopamine in Parkinson's disease they express more highly correlated, rhythmic bursting activity. Patch clamp recording was used to test the hypothesis that dopaminergic modulation reduces the capability of GABAergic inputs to pattern ‘pathological’ activity in STN neurons. Electrically evoked GABA_A receptor-mediated IPSCs exhibited activity-dependent plasticity in STN neurons, i.e. IPSCs evoked at frequencies between 1 and 50 Hz exhibited depression that increased with the frequency of activity. Dopamine, the D₂-like dopamine receptor agonist quinpirole and external media containing a low [Ca²⁺] reduced both the magnitude of IPSCs evoked at 1–50 Hz and synaptic depression at 10–50 Hz. Dopamine/quinpirole also reduced the frequency but not the amplitude of miniature IPSCs recorded in the presence of tetrodotoxin. D₁-like and D₄ agonists were ineffective and D_2/3 but not D4 receptor antagonists reversed the effects of dopamine or quinpirole. Together these data suggest that presynaptic D_2/3 dopamine receptors modulate the short-term dynamics of GABAergic transmission in the STN by lowering the initial probability of transmitter release. Simulated GABA_A receptor-mediated synaptic conductances representative of control or modulated transmission were then generated in STN neurons using the dynamic clamp technique. Dopamine-modulated transmission was less effective at resetting autonomous activity or generating rebound burst firing than control transmission. The data therefore support the conclusion that dopamine acting at presynaptic D₂-like receptors reduces the propensity for GABAergic transmission to generate correlated, bursting activity in STN neurons.

(Received 14 January 2008; accepted after revision 20 February 2008; first published online 21 February 2008)
Corresponding authors M. D. Bevan: Northwestern University, Department of Physiology, Feinberg School of Medicine, 303 E. Chicago Avenue, Chicago, IL 60611, USA. J. Baufreton: Université de Bordeaux 2; Laboratoire Mouvement Adaptation Cognition, UMR CNRS 5227, 146 Rue Léo Saignat, 33076 Bordeaux Cedex, France. Email: jerome.baufreton{at}u-bordeaux2.fr; Email: m-bevan{at}northwestern.edu

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