Amiloride Selectively Blocks the Low Threshold (T) Calcium Channel
- 8 April 1988
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 240 (4849) , 213-215
- https://doi.org/10.1126/science.2451291
Abstract
More than one type of voltage-gated calcium channel has been identified in muscle cells and neurons. Many specific organic and inorganic blockers of the conventional, slowly inactivating high threshold (L) calcium channel have been reported. No specific blockers of the low threshold (T) channel have been as yet identified. Amiloride, a potassium sparing diuretic, has now been shown to selectively block the low threshold calcium channel in mouse neuroblastoma and chick dorsal root ganglion neurons. The selective blockade of the T-type calcium channel will allow identification of this channel in different tissues and characterization of its specific physiological role.This publication has 23 references indexed in Scilit:
- Dominant Role of N-Type Ca 2+ Channels in Evoked Release of Norepinephrine from Sympathetic NeuronsScience, 1988
- Primary structure of the receptor for calcium channel blockers from skeletal muscleNature, 1987
- Development of Two Types of Calcium Channels in Cultured Mammalian Hippocampal NeuronsScience, 1987
- Blockade of current through single calcium channels by Cd2+, Mg2+, and Ca2+. Voltage and concentration dependence of calcium entry into the pore.The Journal of general physiology, 1986
- Kinetic Properties of the Plasma Membrane Na+ -H+ ExchangerAnnual Review of Physiology, 1985
- Three types of neuronal calcium channel with different calcium agonist sensitivityNature, 1985
- Action of organic antagonists on neuronal calcium currentsNeuroscience Letters, 1985
- A low voltage-activated, fully inactivating Ca channel in vertebrate sensory neuronesNature, 1984
- Voltage-dependent block by amiloride and other monovalent cations of apical Na channels in the toad urinary bladderThe Journal of Membrane Biology, 1984
- Are dihydropyridine binding sites voltage sensitive calcium channels?Life Sciences, 1984