Abstract
We used the whole-cell patch-clamp recording technique on surgically excised human retina to examine whether human rod photoreceptors express hyperpolarization-activated cationic currents ( I h) and to analyze the effects of I h on rod’s voltage responses. Hyperpolarizing voltage steps from a holding potential of −60 mV evoked a slow inward-rectifying current in both rods in retinal slices and isolated rods. The slow inward-rectifying currents induced by hyperpolarization were markedly reduced by 3 mM Cs + (a blocker of I h) in the bath, but not by 3 mM Ba 2+ (an anomalous rectifier K + current blocker) or 1 mM SITS (a Cl − current blocker). A concentration–response curve for block by Cs + of the inward currents could be fitted by the Hill equation with a half-blocking concentration (IC 50) of 41 μM and a Hill coefficient of 0.91. The time course of the inward current activation was well described at all recorded voltages by the sum of two exponentials. Under current-clamp conditions, injection of steps of current, either hyperpolarizing or depolarizing, elicited an initial rapid voltage change that was followed by a gradual decay in the voltage response. The decay in the voltage responses was eliminated by bath application of 3 mM Cs +. The voltage dependence, pharmacology, and kinetics of the slow inward-rectifying currents described above suggest that human rods express I h. We suggest that I h becomes activated in the course of large hyperpolarizations generated by bright-light illumination and may modify the waveform of the photovoltage in human rods.
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