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PMID: 6849912 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Effects of divalent and trivalent cations on Na+-Ca2+ exchange in cardiac sarcolemmal vesicles.

Biochimica et biophysica acta ·Vol. 731 ·No. 1 ·1983-05-26 ·Pages 63-8

Trosper TL, Philipson KD

Abstract

Inhibition of Na+-Ca2+ exchange processes in canine cardiac sarcolemmal vesicles by several divalent and trivalent cations has been investigated. The order of cation effectiveness in inhibiting initial rates of Nai+-induced Ca2+ uptake in the presence of 140 mM Nai+ and 20 microM Cao2+ is La3+ greater than Nd3+ greater than Tm3+ approximately Y3+ greater than Cd2+ much greater than Sr2+ greater than Ba2+ approximately Mn2+ much greater than Mg2+. The effectiveness of the divalent ions is related to their ionic crystal radius as compared with that of Ca2+. No such relationship was observed for the trivalent ions, which appeared instead to be more effective the larger their radius. Very low concentrations of trivalent ions ((1-6).10(-7)M) caused slight stimulation of Ca2+-exchange uptake. The trivalent ions also inhibited passive and Nao+-induced Ca2+ efflux from sarcolemmal vesicles, in the same concentration range as that for inhibiting uptake. The divalent ions, however, stimulated Ca2+ efflux, possibly via divalent cation-Ca2+ exchange. These various results suggest that the divalent and trivalent cations interact differently with the exchange apparatus in the sarcolemma.

MeSH Terms
Animals Biological Transport/drug effects Calcium/metabolism Cations/pharmacology Dogs Heart/drug effects Myocardium/metabolism Sarcolemma/drug effects,metabolism Sodium/metabolism
Chemicals
Cations Sodium Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Trosper T L
Philipson K D
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1983-05-26
Pages
63-8
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NHLBI NIH HHS · R01 HL 27821-02 · United States
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