Abstract

Acetylcholine (ACh) is the principal vestibular efferent neurotransmitter among mammalians. Pharmacologic studies prove that ACh activates a small conductance Ca2+-activated K+ channels (KCa) current (SK2), mediated by α9-containing nicotinic ACh receptor (α9nAChR) in mammalian type II vestibular hair cells (VHCs II). However, our studies demonstrate that the m2 muscarinic ACh receptor (m2mAChR) mediates a big conductance KCa current (BK) in VHCs II. To better elucidate the correlation between these two distinct channels in VHCs II of guinea pig, this study was designed to verify whether these two channels and their corresponding AChR subtypes co-exist in the same VHCs II by whole-cell patch clamp recordings. We found that m2mAChR sensitive BK currents were activated in VHCs II isolated by collagenase IA, while α9nAChR sensitive SK2 currents were activated in VHCs II isolated by trypsin. Interestingly, after exposing the patched cells isolated by trypsin to collagenase IA for 3 min, the α9nAChR sensitive SK2 current was abolished, while m2mAChR-sensitive BK current was activated. Therefore, our findings provide evidence that the two distinct channels and their corresponding AChR subtypes may co-exist in the same VHCs II, and the alternative presence of these two ACh receptors-sensitive currents depended on isolating preparation with different enzymes.

Highlights

  • Hair cells in a higher vertebrate’s vestibule are generally divided into two categories: the flask shaped type I vestibular hair cells (VHCs I) and the cylindrical shaped type II vestibular hair cells (VHCs II) [1]

  • We presented our results in three parts: (1) VHCs II isolated by collagenase IA routinely displayed the m2 muscarinic ACh receptor (m2mAChR) sensitive big conductance KCa current (BK) current; (2) VHCs II isolated by trypsin routinely displayed the α9-containing nicotinic ACh receptor (α9nAChR) sensitive SK2 current; (3) After brief exposing the patched cells isolated by trypsin to collagenase IA for 3 min, the α9nAChR sensitive SK2 current was abolished, while a non-inactivating BK current was activated by ACh

  • Our previous finding showed that the BK currents activated by ACh in VHCs II isolated by collagenase IA were mediated by m2mAChR [19], which could be potently inhibited by the BK

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Summary

Introduction

Hair cells in a higher vertebrate’s vestibule are generally divided into two categories: the flask shaped type I vestibular hair cells (VHCs I) and the cylindrical shaped type II vestibular hair cells (VHCs II) [1]. VHCs II are innervated by a number of button-shaped efferent nerve endings, which are cholinergic efferent fibers demonstrated by investigation of ACh-esterase activities in rat [2] and studies of choline acetyltransferase (ChAT) activities in rat [2,3], human [4] and mouse [5]. All these results support that acetylcholine (ACh) is the principal inhibitory neurotransmitter mediating the efferent activities to the vestibule [6]. M1, m2, m5mAChR subtypes have been observed in human vestibular periphery by reverse transcription polymerase chain reaction (RT-PCR)

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