Thapsigargin, A Ca2+-ATPase inhibitor, relaxes rat aorta via nitric oxide formation
- 31 December 1994
- journal article
- research article
- Published by Elsevier in Life Sciences
- Vol. 54 (9) , PL153-PL158
- https://doi.org/10.1016/0024-3205(94)00875-2
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Selective inhibition of agonist‐induced but not shear stress‐dependent release of endothelial autacoids by thapsigarginBritish Journal of Pharmacology, 1993
- Comparison of the Effects of Thapsigargin and BAY K 8644 on Spontaneous Mechanical Activity in Rat Portal Vein and Contractile Responses of Rat Cardiac MuscleBasic & Clinical Pharmacology & Toxicology, 1992
- Capacitative calcium entry revisitedCell Calcium, 1990
- Calcium‐dependent nitric oxide synthesis in endothelial cytosol is mediated by calmodulinFEBS Letters, 1990
- l‐NG‐nitro arginine (l‐NOARG), a novel, l‐arginine‐reversible inhibitor of endothelium‐dependent vasodilatation in vitroBritish Journal of Pharmacology, 1990
- Role of Ca2+-ATPases in regulation of cellular Ca2+ signalling, as studied with the selective microsomal Ca2+-ATPase inhibitor, thapsigarginInflammation Research, 1990
- Effect of calcium on endothelium-derived relaxing factor formation and cGMP levels in endothelial cellsEuropean Journal of Pharmacology, 1989
- Inhibition of vascular smooth muscle relaxation by LY83583Naunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1988
- Effects of Thapsigargin in Isolated Rat Thoracic AortaBasic & Clinical Pharmacology & Toxicology, 1988
- Voltage-activated potassium, but not calcium currents in cultured bovine aortic endothelial cellsPflügers Archiv - European Journal of Physiology, 1987