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Molecular Pharmacology, Vol 15, 620-626, Copyright © 1979 by the American Society for Pharmacology and Experimental Therapeutics

The Harmala Alkaloids: Evidence for Their Complex Inhibition of the K+-Acyl Phosphatase Reaction of Membranes

L. P. SIMONSON 1 and J. S. CHARNOCK 1

1 Department of Pharmacology, University of Alberta, Edmonton, Alberta, T6G 2H7 Canada

Although the harmala alkaloids were originally reported to be specific inhibitors of the Na+-activation site of (Na+ + K+)-ATPase, their reaction is now known to be more complex as the K+-activation site of this enzyme is also thought to be involved. By using a fluorescent method of assay employing 3-O-methyl fluorescein phosphate as substrate, and by appropriate correction of the data for the fluorescence quenching of harmaline itself, we have confirmed that this alkaloid directly interacts with the K+ activation site of the acyl-phosphatase partial reaction of (Na+ + K+)-ATPase. However, calculation of the Hill coefficients for harmaline inhibition of K+-acyl phosphatase and for K+-activation of the system in the presence of harmaline suggests that activation and inhibition do not occur at the same site.

Submitted on June 14, 1978
Accepted on December 4, 1978







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