The effect of 2-n-propyl-3-dimethylamino-5,6-methylenedioxyindene on caffeine-induced contractures of skeletal muscle
- 1 June 1981
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Physiology and Pharmacology
- Vol. 59 (6) , 617-620
- https://doi.org/10.1139/y81-095
Abstract
It has been previously postulated that 2-n-propyl-3-dimethylamino-5,6-methylenedioxyindene (pr-MDI) exhibits calcium antagonistic properties with an intracellular site of action. The present investigation further substantiates this hypothesis by providing evidence that pr-MDI inhibits caffeine-induced contractures (which are mediated by intracellular calcium) of the isolated rat hemidiaphragm skeletal muscle both in the presence and in the absence of extracellular calcium.This publication has 3 references indexed in Scilit:
- Pharmacological evaluation of new calcium antagonists: 2-Substituted 3-dimethylamino-5,6-methylenedioxyindenes. Antiarrhythmic effectsCanadian Journal of Physiology and Pharmacology, 1979
- The role of calcium antagonism in the therapeutic action of drugsCanadian Journal of Physiology and Pharmacology, 1979
- Inhibition of Caffeine Rigor and Radiocalcium Movements by Local Anesthetics in Frog Sartorius MuscleThe Journal of general physiology, 1963