Anethole Supplementation During Oocyte Maturation Improves In Vitro Production of Bovine Embryos

[EN] Oxidative stress is one of the most detrimental factors that affect oocyte developmental competence and embryo development in vitro. The impact of anethole supplementation to in vitro maturation (IVM) media on oocyte maturation and further bovine in vitro embryo production was investigated. Ooc...

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Detalles Bibliográficos
Autores: Sá, Naiza A. R., Vieira, Luís A., Ferreira, Anna Clara A., Cadenas, Jesús, Bruno, Jamily B., Maside Mielgo, Carolina, Sousa, Francisca G. C., Cibin, Francielli W. S., Alves, Benner Geraldo, Rodrigues, Ana Paula R., Leal-Cardoso, José H., Gastal, Eduardo L., Figueiredo, José R.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:España
Institución:Universidad de León
Repositorio:BULERIA. Repositorio Institucional de la Universidad de León
OAI Identifier:oai:buleria.unileon.es:10612/23609
Acceso en línea:https://link.springer.com/article/10.1007/s43032-020-00190-x
https://hdl.handle.net/10612/23609
Access Level:acceso abierto
Palabra clave:Veterinaria
Antioxidant
Anethole
ROS
Mitochondria
Oocyte
Embryo
Descripción
Sumario:[EN] Oxidative stress is one of the most detrimental factors that affect oocyte developmental competence and embryo development in vitro. The impact of anethole supplementation to in vitro maturation (IVM) media on oocyte maturation and further bovine in vitro embryo production was investigated. Oocytes of slaughterhouse-derived bovine ovaries were placed in IVM with anethole at different concentrations of 30 (AN30), 300 (AN300), and 2000 mg/mL (AN2000), or without (control treatment). The oocytes were assessed for maturation rates, and for reactive oxygen species (ROS) and ferric reducing antioxidant power (FRAP) levels, and mitochondrial membrane potential. Embryo development was assessed by cleavage and blastocyst rates, and embryo cell number. The percentage of metaphase II oocytes were similar among the treatments (range, 77%-96%). Anethole at 300 mg/mL was the only treatment that yielded higher cleavage and embryo development (morula and blastocyst) rates compared to the control treatment. The ROS production in the oocytes after maturation did not differ among treatments. However, oocytes treated with anethole at 300 mg/mL had higher (P < .05) FRAP and mitochondrial membrane potential compared to the control treatment. Furthermore, AN300 treatment increased (P < .05) the average number of total cells in blastocysts compared to the control and AN30 treatments. The use of anethole at 300 mg/mL during IVM is suggested to improve the quantity and quality of bovine embryos produced in vitro. The beneficial effects of anethole on embryonic developmental competence in vitro seems to be related to its capacity to regulate the redox balance and improve mitochondrial function in oocytes and embryos.