Abstract

Motoneurons are furnished with a vast repertoire of ionotropic and metabotropic receptors as well as ion channels responsible for maintaining the resting membrane potential and involved in the regulation of the mechanisms underlying its membrane excitability and firing properties. Among them, the GABAA receptors, which respond to GABA binding by allowing the flow of Cl− ions across the membrane, mediate two distinct forms of inhibition in the mature nervous system, phasic and tonic, upon activation of synaptic or extrasynaptic receptors, respectively. In a previous work we showed that furosemide facilitates the monosynaptic reflex without affecting the dorsal root potential. Our data also revealed a tonic inhibition mediated by GABAA receptors activated in motoneurons by ambient GABA. These data suggested that the high affinity GABAA extrasynaptic receptors may have an important role in motor control, though the molecular nature of these receptors was not determined. By combining electrophysiological, immunofluorescence and molecular biology techniques with pharmacological tools here we show that GABAA receptors containing the α6 subunit are expressed in adult turtle spinal motoneurons and can function as extrasynaptic receptors responsible for tonic inhibition. These results expand our understanding of the role of GABAA receptors in motoneuron tonic inhibition.

Highlights

  • The c-aminobutiric acid (GABA) is the major inhibitory neurotransmitter in the mature central nervous system

  • We reported that the monosynaptic reflex evoked by electrical stimulation of one dorsal root in the adult turtle spinal cord was facilitated by furosemide without affecting the dorsal root potential [15]

  • Knowing that furosemide increases the excitability of cerebellar granule cells by blocking extrasynaptic a6 subunit-containing GABAA receptors [8, 9, 20, 21], we decided to test whether the facilitation of the monosynaptic reflex was mediated by a similar mechanism in motoneurons

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Summary

Introduction

The c-aminobutiric acid (GABA) is the major inhibitory neurotransmitter in the mature central nervous system. By activating on specific receptors, GABA inhibits neuronal excitability [1,2,3]. There are two main classes of GABA receptors: GABAA and GABAB. The GABAA receptor is ionotropic and consists of a pentameric protein complex which, in addition to binding sites for GABA, involves binding sites for benzodiazepines, barbiturates and other drugs such as furosemide. In an open state this receptor is preferentially permeable to Cl2 ions. The binding of two molecules of GABA induces its opening and the influx of Cl2 ions causes membrane hyperpolarization [4]. The GABAB receptors, present in the form of dimers, are metabotropic receptors coupled to G proteins [5]

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