THE NA+ K+ ATPASE MEDIATES THE ALPHA(1)-ADRENOCEPTOR STIMULATED INCREASE IN RB-86(+)-UPTAKE IN ISOLATED VENTRICULAR CARDIOMYOCYTES FROM ADULT-RAT HEART/
H. Viko et al., THE NA+ K+ ATPASE MEDIATES THE ALPHA(1)-ADRENOCEPTOR STIMULATED INCREASE IN RB-86(+)-UPTAKE IN ISOLATED VENTRICULAR CARDIOMYOCYTES FROM ADULT-RAT HEART/, Research communications in molecular pathology and pharmacology, 96(1), 1997, pp. 89-106
The aim of the present study was to identify the mechanism(s) responsi
ble for the alpha(1)-adrenoceptor stimulated increase in potassium upt
ake in ventricular cardiomyocytes isolated from adult rat heart. The N
a-/K(-)ATPase blocker ouabain the Na-/K-/2Cl(-)-cotransporter blocker
bumetanide, the Na-/H+-exchanger blocker HOE 694 and the potassium cha
nnel blocker 4-aminopyridine were used as experimental tools. Rb-86(-)
was used as potassium analogue. The basal Rb-86(-)-uptake rate was 0.
25+/-0.01 ml/g protein x min. Maximal alpha(1)-adrenoceptor stimulatio
n increased the Rb-86(+)-uptake 38+/-2 %. Ouabain dose dependently eli
minated the alpha(1)-adrenoceptor stimulated response with a -logIC(50
)-value of 3.64+/-0.23. Bumetanide did not affect the stimulated respo
nse, and there was no effect of bumetanide on the ouabain sensitive co
mponent. HOE 694 and 4-aminopyridine had no effect on the stimulated R
b-86(+)-uptake. Ouabain and HOE 694 also dose dependently inhibited a
portion of the basal Rb-86(+)-uptake (about 60 % and 20 %, respectivel
y), but there was no effect of bumetanide or 4-aminopyridine on the ba
sal Rb-86(+)-uptake. The results show that the Na+/K+ ATPase alone med
iates the alpha(1)-adrenoceptor stimulated increase in potassium uptak
e in this preparation of ventricular cardiomyocytes isolated from adul
t rat heart.