Hypertension, Vol 11, 301-307, Copyright © 1988 by American Heart Association
S Kuriyama, L Hopp, H Tamura, N Lasker and A Aviv
Differences in cellular Na+ and K+ regulation may relate to the
pathogenesis of essential hypertension and the predisposition of blacks to
this disease. To explore these tenets, we examined several aspects of
cellular Na+ homeostasis in serially passed, cultured skin fibroblasts from
30 subjects (15 hypertensive blacks and whites and normotensive subjects
matched for sex, age, and race.) Fibroblasts from blacks demonstrated
higher cellular Na+ turnover rates than did those from whites. This
difference was expressed by accelerated Na+-K+ pump activity
(ouabain-sensitive Na+ washout rate, 3.46 +/- 0.216 for blacks vs 1.84 +/-
0.283 mEq/L/min for whites; p = 0.0006) and a higher rate of cellular
accumulation of Na+ in the presence of ouabain (0.964 +/- 0.0743 vs 0.562
+/- 0.0440 mEq/L/min for blacks and whites, respectively; p = 0.0045).
Associated with these findings, fibroblasts from blacks had higher cellular
Na+ concentration than did those from whites (9.78 +/- 0.512 vs 7.50 +/-
0.400 mEq/L; p = 0.0170, as measured by atomic absorption, and 7.84 +/-
0.470 vs 5.03 +/- 0.980 mEq/L; p = 0.0141, as derived from the equilibrium
distribution ratio of 22Na+). It is concluded that blacks differ from
whites with respect to cellular Na+ turnover rate, which is evidenced by an
increased Na+ influx and accelerated Na+-K+ pump activity in their
fibroblasts. Our findings support the tenet that innate racial differences
in cellular Na+ regulation may underlie the predisposition of blacks to
hypertension.
ARTICLES
A higher cellular sodium turnover rate in cultured skin fibroblasts from blacks
Hypertension Research Center, University of Medicine and Dentistry of New Jersey, Newark 07103.
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