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Published on: February 11, 2011
Voltage-dependent outward K(+) current in intermediate cell of stria vascularis of gerbil cochlea
1Department of Physiology, Kochi Medical School, Nankoku 783-8505, Japan. takeuchi@kochi-ms.ac.jp
Insights
Researchers studied voltage-dependent potassium (K(V)) currents in cochlear stria vascularis melanocytes. This K(V) current stabilizes membrane potential and aids potassium secretion, crucial for hearing.
Area of Science:
- Otolaryngology
- Cell Physiology
- Molecular Biology
Background:
- The stria vascularis in the cochlea maintains the endocochlear potential, essential for hearing.
- Intermediate cells (melanocytes) play a role in cochlear function, but their ion transport mechanisms are not fully understood.
Purpose of the Study:
- To characterize the voltage-dependent outward potassium (K(V)) current in cochlear stria vascularis intermediate cells.
- To investigate the physiological role of this K(V) current in relation to membrane potential and potassium secretion.
Main Methods:
- Whole-cell patch-clamp electrophysiology was used to record K(V) currents.
- Pharmacological agents were employed to identify the properties and blockers of the current.
- Kinetic analysis was performed to describe activation and inactivation properties.
Main Results:
- A distinct K(V) current was identified with a threshold of -80 mV and 50% activation at -42.6 mV.
- The current exhibited slow activation and incomplete inactivation, independent of intracellular calcium.
- Quinine, verapamil, Ba(2+), and tetraethylammonium dose-dependently inhibited the current, while 4-aminopyridine was ineffective.
Conclusions:
- The identified K(V) current likely stabilizes the intermediate cell membrane potential.
- This conductance may contribute to potassium secretion into the intercellular space, influencing the endocochlear potential.
- These findings offer insights into the electrophysiology of cochlear melanocytes and hearing.
Abstract:
A voltage-dependent outward K(+) (K(V)) current in the intermediate cell (melanocyte) of the cochlear stria vascularis was studied using the whole cell patch-clamp technique. The K(V) current had an activation threshold voltage of approximately -80 mV, and 50% activation was observed at -42.6 mV. The time courses of activation and inactivation were well fitted by two exponential functions: the time constants at 0 mV were 7.9 and 58.8 ms for activation and 0.6 and 4.3 s for inactivation. The half-maximal activation time was 13. 8 ms at 0 mV. Inactivation of the current was incomplete even after a prolonged depolarization of 10 s. This current was independent of intracellular Ca(2+). Quinine, verapamil, Ba(2+), and tetraethylammonium inhibited the current in a dose-dependent manner, but 4-aminopyridine was ineffective at 50 mM. We conclude that the K(V) conductance in the intermediate cell may stabilize the membrane potential, which is thought to be closely related to the endocochlear potential, and may provide an additional route for K(+) secretion into the intercellular space.
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