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Veratridine induces a Ca2+ influx,cyclic GMP formation,and backward swimming inParamecium tetraurelia wildtype cells and Ca2+ current-deficient pawn mutant cells
Authors:Joachim E Schultz  Uwe Schade
Institution:(1) Pharmazeutisches Institut der Universität Tübingen, 7400 Tübingen, Federal Republic of Germany
Abstract:Summary Veratridine opens voltage-dependent Na+ channels in many metazoans. InParamecium, which has voltage-dependent Ca2+ channels and a Ca/K action potential, no such Na+ channels are known. A Ca-inward current is correlated to an intracellular increase in cGMP. The addition of veratridine toParamecium wildtype and to pawn mutant cells, which lack the Ca-inward current, transiently increased intracellular levels of cGMP about sevenfold to 40 pmol/mg protein. A half-maximal effect was obtained with 250 mgrm veratridine. The increase in cGMP was maximal about 15 sec after the addition of veratridine and declined rapidly afterwards. Intracellular cAMP levels were not affected. The effect of veratridine on cGMP was dependent on the presence of extracellular Ca2+. The time dependence and extent of stimulation closely resembled the effects observed after stimulation by Ba2+, which causes the repetitive firing of action potentials, Ca-dependent ciliary reversal, and cGMP formation. The effects of Ba2+ and veratridine were not additive. Wildtype cells and, surprisingly, also pawn mutant cells showed avoiding reactions upon addition of veratridine indicating that it induced a Ca2+ influx into the cilia, which causes ciliary reversal. The potency of veratridine to stimulate cGMP formation was little affected by Na+ in wildtype cells, three pawn mutant strains, and in the cell line fast-2, which is defective in a Ca-dependent Na-inward current. Divalent cations (Ca2+, Mg2+, and Ba2+) inhibited the effects the veratridine similar to metazoan cells. The results indicate that veratridine can open the voltage-operated Ca2+ channels inParamecium wildtype and, most interestingly, in pawn mutant cells. The pawn mutation is suggested to represent a defect in the activation of the Ca2+ channel. This explains the lack of differences in ciliary proteins between wildtype and pawn cells reported earlier.
Keywords:mutant  veratridine  calcium channel  cyclic GMP
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