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Two components of voltage-dependent calcium influx in mouse neuroblastoma cells. Measurement with arsenazo III.

Abstract
N1E-115 mouse neuroblastoma cells were injected with the calcium indicator dye arsenazo III. Optical absorbance changes during voltage-clamp depolarization were used to examine the properties of the two calcium currents present in these cells. The rapidly inactivating calcium current (Moolenar and Spector, 1979b, Journal of Physiology, 292:307-323) inactivates by a voltage-dependent mechanism. The slowly inactivating calcium current is dominant in raising intracellular calcium during depolarizations to greater than -20 mV. Lowering the extracellular calcium concentration affects the two calcium currents unequally, with the slowly inactivating current being reduced more. Intracellular calcium falls very slowly (tau greater than 1 min) after a depolarization. The rapidly inactivating calcium current is responsible for a calcium action potential under physiological conditions. In contrast, it is unlikely that the slowly inactivating calcium current has an important electrical role. Rather, its function may be to add a further increment of calcium influx over and above the calcium influx through the rapidly inactivating calcium channels.
AuthorsS R Bolsover
JournalThe Journal of general physiology (J Gen Physiol) Vol. 88 Issue 2 Pg. 149-65 (Aug 1986) ISSN: 0022-1295 [Print] United States
PMID3746249 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Azo Compounds
  • Tetraethylammonium Compounds
  • Arsenazo III
  • Cobalt
  • Tetraethylammonium
  • cobaltous chloride
  • Calcium
Topics
  • Animals
  • Arsenazo III
  • Azo Compounds
  • Calcium (metabolism, pharmacology)
  • Cobalt (metabolism, pharmacology)
  • Electrophysiology
  • Extracellular Space (metabolism)
  • Mice
  • Neuroblastoma (metabolism, physiopathology)
  • Tetraethylammonium
  • Tetraethylammonium Compounds (metabolism, pharmacology)

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