BUFODIENOLIDES AS ENDOGENOUS NA-ATPASE INHIBITORS - BIOSYNTHESIS IN BOVINE AND RAT ADRENALS(,K+)

Citation
D. Lichtstein et al., BUFODIENOLIDES AS ENDOGENOUS NA-ATPASE INHIBITORS - BIOSYNTHESIS IN BOVINE AND RAT ADRENALS(,K+), Clinical and experimental hypertension, 20(5-6), 1998, pp. 573-579
Citations number
16
Categorie Soggetti
Pharmacology & Pharmacy","Peripheal Vascular Diseas
ISSN journal
10641963
Volume
20
Issue
5-6
Year of publication
1998
Pages
573 - 579
Database
ISI
SICI code
1064-1963(1998)20:5-6<573:BAENI->2.0.ZU;2-T
Abstract
The biosynthesis of digitalis-like compounds (DLC) was determined in b ovine and rat adrenal homogenates by following changes in the concentr ation of DLC using three independent sensitive bioassays: inhibition o f [H-3]-ouabain binding to red blood cells and competitive ouabain and bufalin ELISA. The amounts of DLC in bovine and rat adrenal homogenat es, as measured by the two first bioassays, increased with time when t he mixtures were incubated under tissue culture conditions. These resu lts suggest that Na+, K+-ATPase inhibitors which interact with ouabain antibodies, but not those which interact with bufalin antibodies, are synthesized in bovine and rat adrenals.