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J Physiol Volume 566, Number 1, 103-118, July 1, 2005 DOI: 10.1113/jphysiol.2005.087155
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Biophysical and pharmacological characterization of nicotinic cholinergic receptors in rat cochlear inner hair cells

María Eugenia Gómez-Casati1, Paul A Fuchs2, Ana Belén Elgoyhen1 and Eleonora Katz1,3

1 Instituto de Investigaciones en Ingeniería Genética y Biología Molecular, Consejo Nacional de Investigaciones Científicas y Técnicas – Universidad de Buenos Aires, Buenos Aires, Argentina
2 Cochlear Neurotransmission Laboratory, Center for Hearing and Balance, Department of Otolaryngology – Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA
3 Departamento de Fisiología, Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina

Before the onset of hearing, a transient efferent innervation is found on inner hair cells (IHCs). This synapse is inhibitory and mediated by a nicotinic cholinergic receptor (nAChR) probably formed by the {alpha}9 and {alpha}10 subunits. We analysed the pharmacological and biophysical characteristics of the native nAChR using whole-cell recordings from IHCs in acutely excised apical turns of the rat organ of Corti. Nicotine did not activate but rather blocked the acetylcholine (ACh)-evoked currents with an IC50 of 1 ± 0.1 µM. Antagonists of non-cholinergic receptors such as strychnine, bicuculline and ICS-205930 blocked ACh-evoked responses with an IC50 of 8.6 ± 0.8 nM, 59 ± 4 nM and 0.30 ± 0.02 µM, respectively. The IHC nAChR was both permeable to (PCa/PNa = 8 ± 0.9) and modulated by external Ca2+. ACh-evoked currents were potentiated by Ca2+ up to 500 µM but were reduced by higher concentrations of this cation. Ba2+ mimicked the effects of Ca2+ whereas Mg2+ only blocked these currents. In addition, elevation of extracellular Ca2+ reduced the amplitude of spontaneous synaptic currents without affecting their time course. The receptor had an EC50 for ACh of 60.7 ± 2.8 µM in 0.5 mM Ca2+. In the absence of Ca2+, the EC50 for ACh increased, suggesting that potentiation by Ca2+ involves changes in the apparent affinity for the agonist. These pharmacological and biophysical characteristics of the IHC nAChR closely resemble those of the recombinant {alpha}9{alpha}10 nAChR, reinforcing the hypothesis that the functional nAChR at the olivocochlear efferent–IHC synapse is composed of both the {alpha}9 and {alpha}10 subunits.

(Received 23 March 2005; accepted after revision 21 April 2005; first published online 28 April 2005)
Corresponding author Eleonora Katz: INGEBI, Vuelta de Obligado 2490, 1428 Buenos Aires, Argentina. Email: ekatz{at}dna.uba.ar




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