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PMID: 1529757 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Review

Two kinds of calcium-induced release of calcium from the sarcoplasmic reticulum of skinned cardiac cells.

Advances in experimental medicine and biology ·Vol. 311 ·1992-00-00 ·Pages 245-62

Fabiato A

Abstract

This article compares the Ca(2+)-induced release of Ca2+ that is triggered by a rapid increase of free Ca2+ concentration at the outer surface of the sarcoplasmic reticulum of a skinned cardiac cell to the spontaneous release of Ca2+ that is produced by a steady-state high free Ca2+ concentration which overloads the sarcoplasmic reticulum with Ca2+ in a skinned cardiac cell. The first process, that is triggered by a rapid increase of free Ca2+ concentration at the outer surface of the sarcoplasmic reticulum, has a time- and Ca(2+)-dependent activation and inactivation, does not require any preload of the sarcoplasmic reticulum with Ca2+, and is not affected by the addition of inositol (1,4,5)-trisphosphate. The second process, i.e. the spontaneous release of Ca2+ from the sarcoplasmic reticulum, is not inactivated by a high free Ca2+ concentration, requires an overload of the sarcoplasmic reticulum with Ca2+ and is enhanced by inositol(1,4,5)-trisphosphate. The filling inside the sarcoplasmic reticulum with Ca2+ is critical for the triggering of the spontaneous release of Ca2+. On the other hand, the spontaneous release of Ca2+ has many similarities to the "Ca(2+)-induced release of Ca2+" that is observed for isolated sarcoplasmic reticulum vesicles incorporated into a lipid bilayer which is triggered by the increase of free Ca2+ concentration at the outer surface of the sarcoplasmic reticulum. Although the Ca(2+)-induced release of Ca2+ with time- and Ca(2+)-dependent activation and inactivation and the spontaneous release of Ca2+ are regulated by difference mechanisms, they are both inhibited by ryanodine, which suggests that they may take place through the same channel and may even have some partial common pathway.

MeSH Terms
Animals Calcium/metabolism,pharmacology Heart/drug effects Heart Ventricles In Vitro Techniques Kinetics Models, Biological Myocardium/metabolism Rats Sarcoplasmic Reticulum/drug effects,metabolism
Chemicals
Calcium
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Fabiato A
Department of Physiology and Biophysics, Medical College of Virginia, Richmond 23298.
Article Info
Journal
Advances in experimental medicine and biology
Abbr.
Adv Exp Med Biol
ISSN
0065-2598
Published
1992-00-00
Pages
245-62
Language
English
Region
United States
NLM ID
0121103
Subset
IM
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