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J. Biol. Chem., Vol. 262, Issue 8, 3615-3619, Mar, 1987
GD Lopaschuk, M Michalak and H Tsang
Pantothenic acid transport was studied in the isolated perfused rat heart
and isolated sheep cardiac sarcolemmal vesicles. In the perfused heart,
pantothenic acid transport was significantly greater if hearts were
perfused as working hearts rather than Langendorff hearts, but was
unaffected by the perfusion substrates used (11 mM glucose or 1.2 mM
palmitate). Uptake rates of pantothenic acid in working hearts are
dependent on perfusate concentrations of pantothenic acid (a Vmax of 418
nmol/g dry weight/30 min and a Km for pantothenic acid of 10.7 mircoM were
obtained). Reduction in perfusate Na+ concentration from 145 to 105 mM (the
Na+ was replaced with 40 mM choline) resulted in a small but significant
decrease in pantothenic acid uptake. At 145 mM Na+, addition of a mixture
of amino acids, whose uptake is Na+- dependent, resulted in a significant
decrease in pantothenic acid uptake by the heart (173 +/- 5 to 132 +/- 12
nmol/g dry weight). If an inward Na+ gradient in isolated, purified
sarcolemmal vesicles, was imposed, a rapid uptake of pantothenic acid was
observed. Uptake rates are markedly reduced if Na+ was replaced by
equimolar concentrations of K+ or if external Na+ was reduced below 40 mM.
In the presence of Na+, increasing pantothenic acid concentrations resulted
in an increase in pantothenic acid uptake by the vesicles. Combined, these
data demonstrate that pantothenic acid is transported across the myocardial
sarcolemmal membrane by a Na+-dependent mechanism, which may be common to a
number of small molecules.
Regulation of pantothenic acid transport in the heart. Involvement of a Na+-cotransport system
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