The cholinergic efferent inhibition of mammalian outer hair cells (OHCs) is mediated by a hyperpolarizing K+ current. We have made whole-cell tight-seal recordings from single OHCs isolated from the guinea pig cochlea to characterize the mechanism by which acetylcholine (ACh) activates K+ channels. After ACh application, OHCs exhibited a biphasic response: an early depolarizing current preceding the predominant hyperpolarizing K+ current. The current-voltage (I-V) relationship of the ACh-induced response displayed an N-shape, suggesting the involvement of Ca2+ influx. When whole-cell recording was combined with confocal calcium imaging, we simultaneously observed the ACh-induced K+ current (IK(ACh)) and a Ca2+ response restricted to the synaptic area of the cell. This IK(ACh) could be prevented by loading OHCs with 10 mM of the fast Ca2+ buffer bis(2-aminophenoxy)ethane-N,N,N',N'-tetra-acetic acid (or BAPTA), therefore allowing the observation of the ACh-induced early current in isolation. This early current revealed nicotinic features because it activated with an intrinsic delay in the millisecond range, reversed nearly in between potassium and sodium equilibrium potentials, and was blocked by curare. However, it was strongly reduced in the absence of external Ca2+, and its I-V relationship displayed an unusual outward rectification at positive membrane potentials and an inward rectification below -60 mV. The results indicate that the cholinergic response of mammalian OHCs involves a "nicotinic-like" nonspecific cation channel through which Ca2+ enters and triggers activation of nearby Ca2+-dependent K+ channels.

No abstract

No abstract

No abstract

Aminoglycoside antibiotics such as gentamicin are known to block the medial olivocochlear efferent system. In order to determine whether this inhibition takes place at the postsynaptic cholinergic receptors in outer hair cells (OHCs), we studied the effects of these polycationic molecules on cholinergic currents evoked in isolated guinea‐pig OHCs. The cholinergic response of OHCs involves nicotinic‐like receptors (nAChRs) permeable to Ca2+ ions that activate nearby Ca2+‐sensitive K+ channels (KCa(ACh) channels). The extracellular application of gentamicin and neomycin reversibly blocked ACh‐evoked K+ current (IK(ACh)) with IC50 values of 5.5 and 3.2 μm, respectively. The results showed that the blocking mechanism of IK(ACh) was due to inhibition of Ca2+ influx via nAChRs. Our study also provides interesting insights into the functional coupling between nAChRs and KCa(ACh) channels in OHCs. By directly recording the cation current flowing through nAChRs (In(ACh)) using an intracellular solution containing 10 mm BAPTA, we measured an EC50 near 110 μm for ACh‐evoked In(ACh). This EC50 for ACh is one order of magnitude higher than that measured indirectly on IK(ACh). This reveals a rather low affinity of ACh for its receptor but a very efficient coupling between nAChRs and KCa(ACh) channels. We also show that a high external Ca2+ concentration reverts the gentamicin inhibition of IK(ACh) and that gentamicin directly alters the cation current flowing through the nAChRs of OHCs. We propose that gentamicin acts as a non‐competitive cholinergic blocker by displacing Ca2+ from specific binding sites at the nAChRs. This block of the nAChRs at the level of the postsynaptic membrane in OHCs could explain the inhibitory effect of gentamicin reported on the crossed medial olivocochlear efferent system in vivo.

Intracellular photorelease of Ca2+ from caged Ca2+ (DM-nitrophen or nitr5) and the patch-clamp technique in the whole-cell configuration were used to investigate Ca(2+)-activated currents in inner hair cells (IHCs) of the mammalian cochlea. Photoliberation of intracellular Ca2+ activated outward currents with a mean amplitude of 260 +/- 110 pA when IHCs were voltage-clamped, near the resting membrane potential, at -50 mV. The photoactivated currents were reversibly blocked by extracellular application of tetraethylammonium (TEA, 10 mM), neomycin (1 mM) and charybdotoxin (1 microM), but not by apamin. The voltage dependence of membrane currents activated by photolysis of DM-nitrophen demonstrated a reversal potential near the K+ equilibrium potential (Ek) and saturation near 0 mV. The presence of Ca(2+)-activated currents was further confirmed by the effects of extracellular adenosine 5'-triphosphate (ATP, 10 microM) and the Ca2+ ionophore ionomycin (10 microM). Both agents raised intracellular Ca2+ and simultaneously activated outward currents when IHCs were voltage-clamped near the resting membrane potential. In experiments where currents were activated by depolarizing voltage steps, nifedipine (50 microM) and Cd2+ (1 mM) reduced significantly (20-50%) the whole-cell outward currents, suggesting the presence of L-type Ca2+ currents activating K+ currents. These results are the first direct evidence for Ca(2+)-activated K+ currents in mammalian IHCs, these currents being potentially important for cell repolarization during sound-induced depolarization and synaptic transmission.

Simultaneous whole cell patch-clamp and indo 1 fluorescence measurements were used to characterize ATP-evoked membrane currents and intracellular Ca2+ concentration ([Ca2+]i) changes in isolated Hensen cells of the guinea pig organ of Corti. At negative holding potential, ATP activated a biphasic inward current and a concomitant increase in [Ca2+]i. The initial current activated within < 50 ms, showed a reversal potential near 0 mV and was reversibly inhibited by 30 microM suramin, suggesting this conductance was mediated by ATP-gated nonselective cation channels. The delayed ATP-activated current was mainly carried by Cl- as indicated by its shift in reversal potential when intracellular Cl- was replaced by gluconate. This Cl- conductance appeared to be Ca(2+)-activated secondarily to Ca2+ influx, since it required the presence of extracellular Ca2+ and was suppressed when an intracellular solution containing 10 mM 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid was used. In the absence of extracellular Ca2+, ATP still increased [Ca2+]i concomitant with a monophasic inward cation current, indicating Ca2+ release from intracellular stores. We conclude that Hensen cells have ionotropic and metabotropic P2 purinoceptors. They also have Ca(2+)-activated Cl- channels that can be activated by extracellular ATP, suggesting that purinoceptors in Hensen cells could play a regulatory role in ion and water balance of cochlear fluids.

No abstract