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4-aminopyridine and l-cis-diltiazem block the cGMP-activated K+ channels closed by light in the molluscan extra-ocular photoreceptors.

作者信息

Gotow T, Nishi T, Murakami M

机构信息

Department of Physiology, Faculty of Medicine, Kagoshima University, Japan.

出版信息

Brain Res. 1997 Jan 16;745(1-2):303-8. doi: 10.1016/s0006-8993(96)01214-0.

DOI:10.1016/s0006-8993(96)01214-0
PMID:9037422
Abstract

The cGMP-activated K+ channels closed by light lead to the depolarizing photocurrent of photoreceptors in the Onchidium ganglion. Whole-cell current records showed that external application of 100-200 microM 4-aminopyridine or 200-400 microM l-cis-diltiazem completely blocked the macroscopic photocurrent at any depolarizing and hyperpolarizing potentials. Single-channel current recordings suggested that both 4-aminopyridine and l-cis-diltiazem act to block the cGMP-activated K+ channels in their open state from inside the cell.

摘要

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