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Stoichiometry of Na/Ca antiport obtained by magnesium inhibition in cultured vascular smooth muscle cells

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5727408
Cultured smooth muscle cells from rat aorta were loaded with Na, and Na/Ca antiport was assayed by measuring the initial rates of /sup 45/Ca influx and /sup 22/Na efflux. The replacement of extracellular Na with other monovalent ions, usually N-methyl-D-glucamine (NMG), was essential for obtaining significant antiport activity. Mg competitively inhibited /sup 45/Ca influx via the antiporter (Ki = 100 uM). External Ca stimulated /sup 22/Na efflux as expected for antiport activity. Mg did not stimulate /sup 22/Na efflux indicating that Mg is not transported by the antiporter. Mg inhibited Ca-stimulated /sup 22/Na efflux as expected from the /sup 45/Ca influx data. The stoichiometry of the antiporter was calculated from the changes in the rates of /sup 45/Ca influx and /sup 22/Na efflux at 3 Mg concentrations: 2.87 +/- 0.25 (mean +/- SE, n=5). The replacement of external NMG with potassium, but not other monovalent ions (choline, Li), decreased the potency of Mg as an inhibitor of Na/Ca antiport by about 6 fold. Other divalent cations (Co, Mn, Cd, Ba) inhibited Na/Ca antiport and high external potassium decreased the potency of each by about 6 fold. The order of effectiveness of the divalent cations as inhibitors of Na/Ca antiport (Cd>Mn>Co>Ba>Mg) correlated with the crystal ionic radius of the cation.
Research Organization:
Univ. of Alabama, Birmingham
OSTI ID:
5727408
Report Number(s):
CONF-870644-
Conference Information:
Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Journal Volume: 46:6
Country of Publication:
United States
Language:
English

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