Humoral and cellular effects of the K+-channel activator cromakalim in man |
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Authors: | P. Lijnen R. Fagard J. Staessen T. Weiping E. Moerman A. Amery |
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Affiliation: | (1) Hypertension and Cardiovascular Rehabilitation Unit, Department of Pathophysiology, University of Leuven, Leuven, Belgium;(2) Heymans Institute of Pharmacology, University of Gent, Gent, Belgium |
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Abstract: | Summary The effect of cromakalim, a K+-channel activator, on the plasma renin-angiotensin-aldosterone system, catecholamines and -atrial natriuretic peptide, and on the intraerythrocyte concentration and transmembrane fluxes of Na+ and K+ has been investigated in 18 normal male subjects, in a double-blind parallel study. After a run-in period on placebo for 1 week, the subjects were treated either with placebo (n=6) or cromakalim (n=12) for 1 week.Plasma renin activity was significantly increased during cromakalim. No effect of cromakalim on plasma angiotensin II, aldosterone, adrenaline, noradrenaline and -atrial natriuretic peptide was demonstrated. The intra-erythrocyte K+ concentration was decreased during cromakalim administration and Ca2+-dependent K+-channels in red blood cells were increased. |
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Keywords: | cromakalim erythrocyte potassium potassium transport system renin-angiotensin-aldosterone system catecholamines atrial natriuretic peptide |
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