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PMID: 8218911 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Activation of Na-Ca exchange current by photolysis of "caged calcium".

Biophysical journal ·Vol. 65 ·No. 2 ·1993-08-00 ·Pages 882-91

Niggli E, Lederer WJ

Abstract

Intracellular photorelease of Ca2+ from "caged calcium" (DM-nitrophen) was used to investigate the Ca(2+)-activated currents in ventricular myocytes isolated from guinea pig hearts. The patch-clamp technique was applied in the whole-cell configuration to measure membrane current and to dialyze the cytosol with a pipette solution containing the caged compound. In the presence of inhibitors for Ca2+, K+, and Na+ channels, concentration jumps of [Ca2+]i induced a rapidly activating inward Na-Ca exchange current which then decayed slowly (tau approximately 500 ms). The initial peak of the inward current and the time-course of current decay were voltage-dependent, and no reversal of the current direction was found between -100 and +100 mV. The observed shallow voltage dependence can be described in terms of the movement of an apparently fractional elementary charge (+0.44e-) across an energy barrier located symmetrically in the electrical field of the membrane. The currents were dependent on extracellular Na+ with a half-maximal activation at 73 mM and a Hill coefficient of 2.8. No change of membrane conductance was activated by the Ca2+ concentration jump when extracellular Na+ was completely replaced by Li+ or N-methyl-D-glucamine (NMG) or when the Na-Ca exchange was inhibited by extracellular Ni2+, La3+, or dichlorobenzamil (DCB). The velocity of relengthening after a twitch induced by photorelease of Ca2+ was only reduced drastically when both the sarcoplasmic reticulum and the Na-Ca exchange were inhibited suggesting that all other Ca2+ removing mechanisms have a low transport capacity under these conditions. In conclusion, we have used a novel approach to study Na-Ca exchange activity with photolysis of "caged" calcium. We found that in guinea pig heart muscle cells the Na-Ca exchange is a potent mechanism for Ca2+ extrusion, is weakly voltage-dependent (118 mV for e-fold change) and can be studied without contamination with other Ca(2+)-activated currents.

MeSH Terms
Acetates/metabolism Animals Calcium/metabolism Calcium Channels/physiology Carrier Proteins/metabolism Cells, Cultured Chelating Agents/metabolism Ethylenediamines/metabolism Guinea Pigs Heart/drug effects,physiology Heart Ventricles Myocardial Contraction/drug effects,physiology Myocardium/metabolism Nickel/pharmacology Photic Stimulation Photolysis Sodium/metabolism Sodium Channels/physiology Sodium-Calcium Exchanger
Chemicals
Acetates Calcium Channels Carrier Proteins Chelating Agents Ethylenediamines Sodium Channels Sodium-Calcium Exchanger DM-nitrophen Nickel Sodium Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Niggli E
Department of Physiology, University of Bern, Switzerland.
Lederer W J
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40 references, click to expand
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Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
0006-3495
Published
1993-08-00
Pages
882-91
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC1225788
Subset
IM
Grants
NHLBI NIH HHS · HL25675 · United States
NHLBI NIH HHS · HL36974 · United States
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