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J Neurophysiol 96: 2425-2436, 2006. First published July 26, 2006; doi:10.1152/jn.00545.2006
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The Transmembrane Sodium Gradient Influences Ambient GABA Concentration by Altering the Equilibrium of GABA Transporters

Yuanming Wu1, Wengang Wang1 and George B. Richerson1,2,3

1Departments of Neurology and 2Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut; and 3Neurology Service, Veteran's Affairs Medical Center, West Haven, Connecticut

Submitted 21 May 2006; accepted in final form 18 July 2006

Tonic inhibition is widely believed to be caused solely by "spillover" of GABA that escapes the synaptic cleft and activates extrasynaptic GABAA receptors. However, an exclusively vesicular source is not consistent with the observation that tonic inhibition can still occur after blocking vesicular release. Here, we made patch-clamp recordings from neurons in rat hippocampal cultures and measured the tonic current that was blocked by bicuculline or gabazine. During perforated patch recordings, the tonic GABA current was decreased by the GAT1 antagonist SKF-89976a. Zero calcium solution did not change the amount of tonic current, despite a large reduction in vesicular GABA release. Perturbations that would be expected to alter the transmembrane sodium gradient influenced the tonic current. For example, in zero calcium Ringer, TTX (which can decrease cytosolic [Na+]) reduced tonic current, whereas veratridine (which can increase cytosolic [Na+]) increased tonic current. Likewise, removal of extracellular sodium led to a large increase in tonic current. The increases in tonic current induced by veratridine and sodium removal were completely blocked by SKF89976a. When these experiments were repeated in hippocampal slices, similar results were obtained except that a GAT1- and GAT3-independent nonvesicular source(s) of GABA was found to contribute to the tonic current. We conclude that multiple sources can contribute to ambient GABA, including spillover and GAT1 reversal. The source of GABA release may be conceptually less important in determining the amount of tonic inhibition than the factors that control the equilibrium of GABA transporters.


Address for reprint requests and other correspondence: G. B. Richerson, Neurology, LCI-712B, Yale University School of Medicine, 15 York St., PO 208018, New Haven, CT 06520-8018 (E-mail: George.Richerson{at}Yale.Edu)




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K. K. Ade, M. J. Janssen, P. I. Ortinski, and S. Vicini
Differential Tonic GABA Conductances in Striatal Medium Spiny Neurons
J. Neurosci., January 30, 2008; 28(5): 1185 - 1197.
[Abstract] [Full Text] [PDF]




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