Plant alkaloids, tetrandrine and hernandezine, inhibit calcium-depletion stimulated calcium entry in human and bovine endothelial cells
- 1 May 1996
- journal article
- Published by Elsevier in Life Sciences
- Vol. 58 (25) , 2327-2335
- https://doi.org/10.1016/0024-3205(96)00233-0
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Tetrandrine: A new ligand to block voltage-dependent Ca2+ and Ca2+-activated K+ channelsLife Sciences, 1994
- Different mechanisms can activate Ca2+ entrance via cation currents in endothelial cellsLife Sciences, 1994
- Plant‐derived drugs acting on cellular ca 2+ mobilization in vascular smooth muscle: Tetramethylpyrazine and tetrandrineThe International Journal of Cell Cloning, 1994
- Emptying of intracellular Ca2+ stores releases a novel small messenger that stimulates Ca2+ influxNature, 1993
- Tetrandrine: a vasodilator of medicinal herb origin with a novel contractile effect on dog saphenous veinEuropean Journal of Pharmacology, 1993
- Depletion of intracellular calcium stores activates a calcium current in mast cellsNature, 1992
- Tetrandrine: A novel calcium channel antagonist inhibits type I calcium channels in neuroblastoma cellsNeuropharmacology, 1991
- SK&F 96365, a novel inhibitor of receptor-mediated calcium entryBiochemical Journal, 1990
- Inhibition by tetrandrine of calcium currents at mouse motor nerve endingsBrain Research, 1990
- A model for receptor-regulated calcium entryCell Calcium, 1986