TY - JOUR
T1 - Stimulation of potassium efflux in rat liver by a low dose of thyroid hormone
T2 - Evidence for enhanced cation permeability in the absence of Na, K-ATPase induction
AU - Haber, Richard S.
AU - Loeb, John N.
PY - 1986/1
Y1 - 1986/1
N2 - The effects of a low dose of T3 on passive cellular K+ efflux and Na, K-ATPase activity were studied in hypothyroid rat liver. Male Sprague-Dawley rats were rendered hypothyroid by 4 weeks of a low iodine diet with 0.5% NaCIO4added to the drinking water, and for the last 2 weeks of this period received daily sc injections of either T3 (1 μg/100 g BW) or diluent alone. At the end of this time, both the passive efflux of 86Rb+ (a K+ analog) from liver slices isotopically prelabeled in vitro and Na, K-ATPase activity in liver homogenates were determined. The T3 treatment regimen resulted in a 55% increase in the 86Rb+ efflux rate constant (P < 0.003), while, in contrast, Na, K-ATPase activity remained unchanged. These results show that T3, even at a low dose, enhances passive K+ efflux from liver slices and that, consistent with previous observations, this enhancement can occur in the absence of any detectable change in the number of Na, K pumps. Since the rate of Na, K pump function appears in general to be limited by the rate of passive cation permeation, rather than by Na, K pump number per se, these observations provide additional evidence that increased cation permeability may play a role in the stimulation of active cation transport by thyroid hormone.
AB - The effects of a low dose of T3 on passive cellular K+ efflux and Na, K-ATPase activity were studied in hypothyroid rat liver. Male Sprague-Dawley rats were rendered hypothyroid by 4 weeks of a low iodine diet with 0.5% NaCIO4added to the drinking water, and for the last 2 weeks of this period received daily sc injections of either T3 (1 μg/100 g BW) or diluent alone. At the end of this time, both the passive efflux of 86Rb+ (a K+ analog) from liver slices isotopically prelabeled in vitro and Na, K-ATPase activity in liver homogenates were determined. The T3 treatment regimen resulted in a 55% increase in the 86Rb+ efflux rate constant (P < 0.003), while, in contrast, Na, K-ATPase activity remained unchanged. These results show that T3, even at a low dose, enhances passive K+ efflux from liver slices and that, consistent with previous observations, this enhancement can occur in the absence of any detectable change in the number of Na, K pumps. Since the rate of Na, K pump function appears in general to be limited by the rate of passive cation permeation, rather than by Na, K pump number per se, these observations provide additional evidence that increased cation permeability may play a role in the stimulation of active cation transport by thyroid hormone.
UR - https://www.scopus.com/pages/publications/0022631514
U2 - 10.1210/endo-118-1-207
DO - 10.1210/endo-118-1-207
M3 - Article
C2 - 2416552
AN - SCOPUS:0022631514
SN - 0013-7227
VL - 118
SP - 207
EP - 211
JO - Endocrinology
JF - Endocrinology
IS - 1
ER -