Amphibian oocyte maturation and protein synthesis: related inhibition by cyclic AMP, theophylline, and papaverine
Author
dc.contributor.author
Bravo, Roberto
Author
dc.contributor.author
Otero,
Author
dc.contributor.author
Allende, S.
Author
dc.contributor.author
Allende, S.
Admission date
dc.date.accessioned
2019-01-29T15:46:01Z
Available date
dc.date.available
2019-01-29T15:46:01Z
Publication date
dc.date.issued
1978
Cita de ítem
dc.identifier.citation
Proceedings of the National Academy of Sciences of the United States of America, Volumen 75, Issue 3, 2018, Pages 1242-1246
Identifier
dc.identifier.issn
00278424
Identifier
dc.identifier.other
10.1073/pnas.75.3.1242
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/162307
Abstract
dc.description.abstract
Two inhibitors of cyclic AMP phosphodiesterase (3':5'-cyclic-AMP 5'-nucleotidohydrolase, EC 3.1.4.17), theophylline and papaverine, inhibit the maturation of Xenopus laevis oocytes induced by 4 different stimuli: human chorionic gonadotropin, progesterone, testosterone, and lanthanum ions. Addition of 1 mM cyclic AMP to the medium delays maturation by approximately 2 hr. Papaverine, theophylline, and cyclic AMP inhibit amino acid incorporation into oocyte proteins by 50% or more but do not inhibit amino acid uptake. The capacity of theophylline to block maturation and protein synthesis is reversed in a parallel fashion by addition of 1-5 mM calcium ion to the medium. Addition of papaverine, theophylline, and cycloheximide to oocytes at different times after hormonal treatment shows that the step sensitive to blockage by the 3 drugs is coincident and precedes germinal vesicle breakdown by about 1.5 hr. Theophylline and papaverine do not increase endogenous cyclic AMP levels observed 3 h