dc.creatorMedina, María Fernanda
dc.creatorBühler, M. I.
dc.creatorSeisdedos de Sánchez Toranzo, Graciela del Valle
dc.date.accessioned2017-12-28T17:56:36Z
dc.date.accessioned2018-11-06T15:37:33Z
dc.date.available2017-12-28T17:56:36Z
dc.date.available2018-11-06T15:37:33Z
dc.date.created2017-12-28T17:56:36Z
dc.date.issued2014-11
dc.identifierMedina, María Fernanda; Bühler, M. I.; Seisdedos de Sánchez Toranzo, Graciela del Valle; Chemical activation in Rhinella arenarum oocytes: effect of dehydroleucodine (DhL) and its hydrogenated derivative (2H-DhL); Cambridge University Press; Zygote; 26; 3; 11-2014; 924-932
dc.identifier0967-1994
dc.identifierhttp://hdl.handle.net/11336/31837
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1899227
dc.description.abstractMature oocytes are arrested in metaphase II due to the presence of high levels of active maturation promoting factor (MPF). After fertilization, active MPF levels decline abruptly, enabling oocytes to complete meiosis II. One of the first and universal events of oocyte activation is an increase in cytosolic Ca2+ that would be responsible for MPF inactivation. Mature oocytes can also be activated by parthenogenetic activation. The aims of this work are to test the ability of dehydroleucodine (DhL) and its hydrogenated derivative 11,13-dihydro-dehydroleucodine (2H-DhL) to induce chemical activation in amphibian oocytes and to study the participation of calcium in the process. Results indicated that DhL and 2H-DhL induced oocyte activation in a dose-dependent manner. After 90 min of treatment, DhL 36 μM was able to induce 95% activation, while 2H-DhL 36 μM was less active, with only 40% activation. Our results suggest that DhL induced the inhibition of MPF activity, probably by an increase in intracellular Ca2+ concentration. Extracellular Ca2+ would not be significant, although Ca2+ release from intracellular stores is critical. In this sense, IP3Rs and RyRs were involved in the Ca2+ transient induced by lactones. In this species, RyRs appears to be the largest contributor to Ca2+ release in DhL-induced activation. Although more studies are needed on the mechanism of action through which these lactones induce oocyte activation in Rhinella arenarum, the results of this research provide interesting perspectives for the use of these lactones as chemical activators in in vitro fertilization and cloning.
dc.languageeng
dc.publisherCambridge University Press
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1017/S0967199414000641
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.cambridge.org/core/journals/zygote/article/chemical-activation-in-rhinella-arenarum-oocytes-effect-of-dehydroleucodine-dhl-and-its-hydrogenated-derivative-2hdhl/396294A2DA82D73E2F9C0C156E3716A4
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectCalcium
dc.subjectDehydroleucodine
dc.subjectOocyte activation
dc.subjectRhinella arenarum
dc.titleChemical activation in Rhinella arenarum oocytes: effect of dehydroleucodine (DhL) and its hydrogenated derivative (2H-DhL)
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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