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L-type and R-type Ca
2+ currents were detected in frog semicircular canal hair cells. The former was noninactivating and nifedipine-sensitive (5
μM); the latter, partially inactivated, was resistant to ω-conotoxin GVIA (5
μM), ω-conotoxin MVIIC (5
μM), and ω-agatoxin IVA (0.4
μM), but was sensitive to mibefradil (10
μM). Both currents were sensitive to Ni
2+ and Cd
2+ (>10
μM). In some cells the L-type current amplitude increased almost twofold upon repetitive stimulation, whereas the R-type current remained unaffected. Eventually, run-down occurred for both currents, but was prevented by the protease inhibitor calpastatin. The R-type current peak component ran down first, without changing its plateau, suggesting that two channel types generate the R-type current. This peak component appeared at −40
mV, reached a maximal value at −30
mV, and became undetectable for voltages ≥0
mV, suggestive of a novel transient current: its inactivation was indeed reversibly removed when Ba
2+ was the charge carrier. The L-type current and the R-type current plateau were appreciable at −60
mV and peaked at −20
mV: the former current did not reverse for voltages up to +60
mV, the latter reversed between +30 and +60
mV due to an outward Cs
+ current flowing through the same Ca
2+ channel. The physiological role of these currents on hair cell function is discussed.