Analysis of the activity of oncocalyxone A (Auxemma oncocalyx) and doxorubicin on the in vitro development of porcine oocytes

Most anticancer drugs like doxorubicin (DXR) have low specificity that results in undesirable effects especially when it comes to collateral effects on reproduction. Plants are excellent sources when searching for new drugs. Auxemma oncocalyx (A. oncocalyx) and its main component Oncocalyxone A (onc...

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Veröffentlicht in:Revista de la Sociedad Científica del Paraguay 2019-12, Vol.24 (2), p.274-292
Hauptverfasser: Leiva Revilla, Johanna, Maside, Carolina, Vieira, Luis, Cadenas, Jesús, Acioly, Ana Clara Ferreira, Paes, Victor Macedo, Agiar, Francisco Leo, Celestino, Juliana Jales de Hollanda, Alves, Benner Geraldo, Pessoa, Otilia Deusdenia Loiola, Toniolli, Ricardo, Rodrigues, Ana Paula, Figueiredo, José Ricardo de
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Sprache:eng ; por ; spa
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Zusammenfassung:Most anticancer drugs like doxorubicin (DXR) have low specificity that results in undesirable effects especially when it comes to collateral effects on reproduction. Plants are excellent sources when searching for new drugs. Auxemma oncocalyx (A. oncocalyx) and its main component Oncocalyxone A (onco A) have anti-tumoral activity and are less toxic than DXR in reproductive parameters. However, there are no studies on the action of these drugs regarding the porcine in vitro oocyte competence and embryo development. The aim of this study was to evaluate the effect of A. oncocalyx and onco A exposure during in vitro maturation (IVM) of oocytes (Experiment 1) or in vitro embryo culture (IVC) (Experiment 2) on the oocyte developmental competence. For experiment 1, COCs were distributed in IVM medium alone (control) or supplemented with DXR (0.3 g/mL), A. oncocalyx (1.2 g/mL) and onco A (1 g/mL). Then, oocytes were submitted to in vitro fertilization (IVF) and in vitro embryo culture. For experiment 2, zygotes were cultured with DXR, A. oncocalyx and onco A for 7 days. Viability, maturation, fertilization and embryo developmental parameters were evaluated in both experiments. In experiment 1; DXR, A. oncocalyx and onco A reduced (P
ISSN:0379-9123
2617-4731
DOI:10.32480/rscp.2019-24-2.274-292