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

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...

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Veröffentlicht in:British journal of pharmacology 1993-10, Vol.110 (2), p.519-520
Hauptverfasser: Bkaily, Ghassan, D'Orléans‐Juste, Pedro, Naik, Radha, Pérodin, Jacqueline, Stankova, Jana, Abdulnour, Elias, Rola‐Pleszczynski, Marek
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Sprache:eng
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Zusammenfassung: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.
ISSN:0007-1188
1476-5381
DOI:10.1111/j.1476-5381.1993.tb13841.x