PAF activation of a voltage‐gated R‐type Ca2+ channel in human and canine aortic endothelial cells

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Abstract

By the use of fura‐2 and digital imaging techniques, [K]o depolarization or PAF (10−9 m) were shown to induce a sustained increase of [Ca]i in human or canine single aortic vascular endothelial cells (VEC) that was insensitive to nifedipine but sensitive to (−)‐PN200–110 or to lowering of [Ca]o. The PAF‐induced effect on [Ca]i was blocked by the PAF receptor antagonist, WEB2170. Our results suggest that [K]o depolarization and PAF increase [Ca]i via the activation of R‐type Ca2+ channels. 1993 British Pharmacological Society

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Bkaily, G., D’Orléans‐Juste, P., Naik, R., Pérodin, J., Stankova, J., Abdulnour, E., & Rola‐Pleszczynski, M. (1993). PAF activation of a voltage‐gated R‐type Ca2+ channel in human and canine aortic endothelial cells. British Journal of Pharmacology, 110(2), 519–520. https://doi.org/10.1111/j.1476-5381.1993.tb13841.x

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