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1.
Oxid Med Cell Longev ; 2022: 7113793, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35237383

RESUMEN

α-Ketoglutarate (α-KG) is a metabolite in the tricarboxylic acid cycle. It has a strong antioxidant function and can effectively prevent oxidative damage. Previous studies have shown that α-KG exists in porcine follicles, and its content gradually increases as the follicles grow and mature. However, the potential mechanism of supplementation of α-KG on porcine oocytes during in vitro maturation (IVM) has not yet been reported. The purpose of this study was to explore the effect of α-KG on the early embryonic development of pigs and the mechanisms underlying these effects. We found that α-KG can enhance the development of early pig embryos. Adding 20 µM α-KG to the in vitro culture medium significantly increased the rate of blastocyst formation and the total cell number. Compared with to that of the control group, apoptosis in blastocysts of the supplement group was significantly reduced. α-KG reduced the production of reactive oxygen species and glutathione levels in cells. α-KG not only improved the activity of mitochondria but also inhibited the occurrence of apoptosis. After supplementation with α-KG, pig embryo pluripotency-related genes (OCT4, NANOG, and SOX2) and antiapoptotic genes (Bcl2) were upregulated. In terms of mechanism, α-KG activates the Nrf2/ARE signaling pathway to regulate the expression of antioxidant-related targets, thus combating oxidative stress during the in vitro culture of oocytes. Activated Nrf2 promotes the transcription of Bcl2 genes and inhibits cell apoptosis. These results indicate that α-KG supplements have a beneficial effect on IVM by regulating oxidative stress during the IVM of porcine oocytes and can be used as a potential antioxidant for IVM of porcine oocytes.


Asunto(s)
Antioxidantes/farmacología , Desarrollo Embrionario/efectos de los fármacos , Ácidos Cetoglutáricos/farmacología , Meiosis/efectos de los fármacos , Factor 2 Relacionado con NF-E2/metabolismo , Oocitos/metabolismo , Oogénesis/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Transducción de Señal/efectos de los fármacos , Animales , Apoptosis/efectos de los fármacos , Blastocisto/metabolismo , Medios de Cultivo/química , Suplementos Dietéticos , Embrión de Mamíferos/efectos de los fármacos , Embrión de Mamíferos/metabolismo , Femenino , Glutatión/metabolismo , Técnicas de Maduración In Vitro de los Oocitos/métodos , Mitocondrias/metabolismo , Oocitos/efectos de los fármacos , Embarazo , Especies Reactivas de Oxígeno/metabolismo , Porcinos
2.
Reprod Domest Anim ; 55(9): 1072-1079, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-32531853

RESUMEN

Reactive oxygen species (ROS) damage mammalian sperm during liquid storage. Notoginsenoside R1 (NR1) is a compound isolated from the roots of Panax notoginseng; it has powerful ROS-scavenging activities. This work hypothesized that the antioxidant capacity of NR1 could improve boar sperm quality and fertility during liquid storage. During liquid storage at 17°C, the supplementation of semen extender with NR1 (50 µM) significantly improved sperm motility, membrane integrity and acrosome integrity after 5 days of preservation. NR1 treatment also reduced ROS and lipid peroxidation (LPO) levels at day 5 (p <0.05). Higher glutathione (GSH), superoxide dismutase (SOD), catalase (CAT) levels and sperm-zona pellucida binding capacity were observed in the 50 µM NR1 group than those in the control group at day 7 (p <0.05). Importantly, statistical analysis of the fertility of 200 sows indicated that addition of NR1 to the extender improved the fertility parameters of boar spermatozoa during liquid storage at 17°C (p <0.05). These results demonstrate the practical feasibility of using 50 µM NR1 as an antioxidant in boar extender during liquid storage at 17°C, which is beneficial to both spermatozoa quality and fertility.


Asunto(s)
Ginsenósidos/farmacología , Preservación de Semen/veterinaria , Espermatozoides/fisiología , Sus scrofa , Acrosoma , Animales , Antioxidantes/farmacología , Catalasa/análisis , Femenino , Fertilización In Vitro , Glutatión/análisis , Peroxidación de Lípido , Masculino , Especies Reactivas de Oxígeno/metabolismo , Preservación de Semen/métodos , Motilidad Espermática/efectos de los fármacos , Superóxido Dismutasa/análisis , Zona Pelúcida/metabolismo
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