Abstract

The intracellular arsenazo signal indicating the transient light-evoked change in cytosolic Ca 2+ (or Sr 2+) concentration was measured in Limulus ventral photoreceptors simultaneously with the receptor current under voltage clamp conditions at 15°C. The latency of the light-evoked arsenazo response was consistently more than 25m sec longer than the latency of the electrical light response (receptor current cr — potential). Replacing calcium by strontium in the superfusate caused, within 30–40min, reversible changes: an enlargement of the arsenazo response and a considerable prolongation of both latencies, that of the electrical and that of the arsenazo response; the difference between the two latencies, however, stayed essentially constant.

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