Inhibition of endogenous ouabain by atrial natriuretic peptide is a guanylyl cyclase independent effect

Background Endogenous ouabain (EO) and atrial natriuretic peptide (ANP) are important in regulation of sodium and fluid balance. There is indirect evidence that ANP may be involved in the regulation of endogenous cardenolides. Methods H295R are human adrenocortical cells known to release EO. Cells w...

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Veröffentlicht in:PloS one 2021-11, Vol.16 (11), p.e0260131-e0260131, Article 0260131
Hauptverfasser: Tegin, Gulay, Gao, Yonglin, Hamlyn, John M., Clark, Barbara J., El-Mallakh, Rif S.
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Sprache:eng
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Zusammenfassung:Background Endogenous ouabain (EO) and atrial natriuretic peptide (ANP) are important in regulation of sodium and fluid balance. There is indirect evidence that ANP may be involved in the regulation of endogenous cardenolides. Methods H295R are human adrenocortical cells known to release EO. Cells were treated with ANP at physiologic concentrations or vehicle (0.1% DMSO), with or without guanylyl cyclase inhibitor 1,2,4 oxadiazolo[4,3-a]quinoxalin-1-one (ODQ). Cyclic guanosine monophosphate (cGMP), the intracellular second messenger of ANP, was measured by a chemiluminescent immunoassay and EO was measured by radioimmunoassay of C18 extracted samples. Results EO secretion is inhibited by ANP treatment, with the most prolonged inhibition (90 min vs
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0260131