Effects of Alterations in Cell Phenotype and Hypokalemia on Sodium-Potassium Pump Activity in Rabbit Vascular Smooth Muscle
- 1 January 1985
- journal article
- research article
- Published by Taylor & Francis in Clinical and Experimental Hypertension. Part A: Theory and Practice
- Vol. 7 (11) , 1563-1582
- https://doi.org/10.3109/10641968509073610
Abstract
We investigated in cell culture, how alterations in phenotype accompanying proliferation of rabbit aortic smooth muscle and chronic hypokalemia could affect the Na, K pump. Total rubidium-86 uptake as well as ouabain and frusemide-sensitive uptake into cells was measured in physiological salts solution (PSS), PSS containing 5% foetal calf serum and PSS containing foetal calf serum plus 15μM monensin. In physiological salts solution 90% of the rubidium-86 uptake into contractile or synthetic state cells was frusemide-sensitive and less than 8% ouabain-sensitive. Total and frusemide-sensitive rubidium-86 uptakes, measured in PSS or PSS containing foetal calf serum were similar in cells cultured and maintained in the contractile phenotype, cells in the synthetic phenotype and those which had recently reverted from the synthetic to contractile phenotype. When cells were sodium loaded in the presence of monensin and foetal calf serum, ouabain-sensitive rubidium-86 uptake was 50% higher in cells which were maintained in culture in the contractile phenotype. Frusemide-sensitive rubidium-86 uptake was similar in each cell phenotype. To examine how cell culture in hypokalemic media would affect the Na, K pump, we determined ouabain-sensitive rubidium-86 uptake in the presence of monensin plus foetal calf serum in cells incubated for 24 hours in low and normal potassium containing culture media. Ouabain-sensitive uptake was 20% higher in cells cultured in a 0.76mM potassium medium than i n those cultured i n 5.4mM potassium medium. Frusemide-sensitive rubidium-86 uptake was unaffected. These results demonstrate that ‘maximal’ Na, K pump activity in sodium-loaded cells is reduced when cells change from the contractile to synthetic phenotype. This reduction appears only very slowly reversible when cells revert from the synthetic to contractile phenotype. Prolonged hypokalemia increases ‘maximal’ activity of the Na, K pump.Keywords
This publication has 32 references indexed in Scilit:
- Regulation of Na/K/Cl cotransport in vascular smooth muscle cellsBiochemical and Biophysical Research Communications, 1984
- Dietary Chloride as a Determinant of "Sodium-Dependent" HypertensionScience, 1983
- Sodium and potassium ion transport accelerations in erythrocytes of DOC, DOC-salt, two-kidney, one clip, and spontaneously hypertensive rats. Role of hypokalemia and cell volume.Hypertension, 1983
- Changes in erythrocyte sodium, sodium transport and 3H ouabain binding capacity during digoxin administration in the pigLife Sciences, 1983
- Function of the sodium pump in arterial smooth muscle in experimental hypertension: role of pressure.Hypertension, 1982
- Increased circulating levels of an endogenous digoxin-like factor in hypertensive monkeys.Hypertension, 1982
- Sodium fluxes in human fibroblasts: Effect of serum, Ca+2, and amilorideJournal of Cellular Physiology, 1981
- Sodium pump activity in arteries of Dahl salt-sensitive rats.Hypertension, 1981
- Na entry and Na‐K pump activity in murine, hamster, and human cells ‐ effect of monensin, serum, platelet extract, and viral transformationJournal of Cellular Physiology, 1980
- Cell growth and ouabain-sensitive 86Rb+ uptake and (Na+ + K+)-ATPase activity in 3T3 and SV40 transformed 3T3 fibroblastsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1976