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The Journal of Neuroscience, December 5, 2007, 27(49):13552-13566; doi:10.1523/JNEUROSCI.3430-07.2007

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Cellular/Molecular
Nav1.6 Sodium Channels Are Critical to Pacemaking and Fast Spiking in Globus Pallidus Neurons

Jeff N. Mercer, C. Savio Chan, Tatiana Tkatch, Joshua Held, and D. James Surmeier

Department of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611

Correspondence should be addressed to D. James Surmeier, Department of Physiology, Feinberg School of Medicine, Northwestern University, 303 East Chicago Avenue, Chicago, IL 60611. Email: j-surmeier{at}northwestern.edu

Neurons in the external segment of the globus pallidus (GPe) are autonomous pacemakers that are capable of sustained fast spiking. The cellular and molecular determinants of pacemaking and fast spiking in GPe neurons are not fully understood, but voltage-dependent Na⁺ channels must play an important role. Electrophysiological studies of these neurons revealed that macroscopic activation and inactivation kinetics of their Na⁺ channels were similar to those found in neurons lacking either autonomous activity or the capacity for fast spiking. What was distinctive about GPe Na⁺ channels was a prominent resurgent gating mode. This mode was significantly reduced in GPe neurons lacking functional Nav1.6 channels. In these Nav1.6 null neurons, pacemaking and the capacity for fast spiking were impaired, as was the ability to follow stimulation frequencies used to treat Parkinson's disease (PD). Simulations incorporating Na⁺ channel models with and without prominent resurgent gating suggested that resurgence was critical to fast spiking but not to pacemaking, which appeared to be dependent on the positioning of Na⁺ channels in spike-initiating regions of the cell. These studies not only shed new light on the mechanisms underlying spiking in GPe neurons but also suggest that electrical stimulation therapies in PD are unlikely to functionally inactivate neurons possessing Nav1.6 Na⁺ channels with prominent resurgent gating.

Key words: patch clamp; Parkinson's disease; deep brain stimulation; scRT-PCR; burst firing; Nav1.6; Nav1.1; resurgent; basal ganglia; NEURON; med^TG

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Received Dec. 6, 2006; revised Oct. 2, 2007; accepted Oct. 2, 2007.

Correspondence should be addressed to D. James Surmeier, Department of Physiology, Feinberg School of Medicine, Northwestern University, 303 East Chicago Avenue, Chicago, IL 60611. Email: j-surmeier{at}northwestern.edu

This article has been cited by other articles:

				C. Gunay, J. R. Edgerton, and D. Jaeger Channel Density Distributions Explain Spiking Variability in the Globus Pallidus: A Combined Physiology and Computer Simulation Database Approach J. Neurosci., July 23, 2008; 28(30): 7476 - 7491. [Abstract] [Full Text] [PDF]

				A. H. Gittis and S. du Lac Similar Properties of Transient, Persistent, and Resurgent Na Currents in GABAergic and Non-GABAergic Vestibular Nucleus Neurons J Neurophysiol, May 1, 2008; 99(5): 2060 - 2065. [Abstract] [Full Text] [PDF]

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