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Role of astaxanthin as an efficient antioxidant on the in vitro maturation and vitrification of porcine oocytes.
Xiang, De-Cai; Jia, Bao-Yu; Fu, Xiang-Wei; Guo, Jian-Xiong; Hong, Qiong-Hua; Quan, Guo-Bo; Wu, Guo-Quan.
Afiliação
  • Xiang DC; Yunnan Provincial Engineering Laboratory of Animal Genetic Resource Conservation and Germplasm Enhancement, Yunnan Animal Science and Veterinary Institute, Kunming, Yunnan, 650224, China.
  • Jia BY; College of Veterinary Medicine, Yunnan Agricultural University, Kunming, Yunnan, 650201, China.
  • Fu XW; College of Animal Science and Technology, China Agricultural University, Haidian District, Beijing, 100193, China.
  • Guo JX; College of Veterinary Medicine, Yunnan Agricultural University, Kunming, Yunnan, 650201, China.
  • Hong QH; Yunnan Provincial Engineering Laboratory of Animal Genetic Resource Conservation and Germplasm Enhancement, Yunnan Animal Science and Veterinary Institute, Kunming, Yunnan, 650224, China.
  • Quan GB; Yunnan Provincial Engineering Laboratory of Animal Genetic Resource Conservation and Germplasm Enhancement, Yunnan Animal Science and Veterinary Institute, Kunming, Yunnan, 650224, China. Electronic address: waltq20020109@163.com.
  • Wu GQ; Yunnan Provincial Engineering Laboratory of Animal Genetic Resource Conservation and Germplasm Enhancement, Yunnan Animal Science and Veterinary Institute, Kunming, Yunnan, 650224, China. Electronic address: wuguoquan1982@163.com.
Theriogenology ; 167: 13-23, 2021 Jun.
Article em En | MEDLINE | ID: mdl-33743504
ABSTRACT
As one of the most powerful natural antioxidants, astaxanthin (Ax) has begun to be applied to the field of reproductive biology. Here we used porcine oocyte as a model to explore how Ax improves the oocyte potential during in vitro maturation (IVM), and we also investigated the cytoprotective effects of Ax on the vitrified oocytes. Ax supplementation (final concentration of 2.5 µM) was subjected for immature oocytes during vitrification and subsequent IVM; fresh oocytes were also matured in vitro in the presence or absence of 2.5 µM Ax. Our results showed that Ax significantly increased the survival rate of vitrified oocytes, and promoted the blastocyst yield of both fresh and vitrified oocytes after parthenogenetic activation and somatic cell nuclear transfer. The oocytes treated with Ax displayed significantly lower reactive oxygen species generation and higher glutathione level. Vitrification of oocytes had no impact on caspase-3, cathepsin B and autophagic activities; Ax significantly decreased the cathepsin B activity in both fresh and vitrified oocytes. Moreover, the relative fluorescence intensity of lysosomes was significantly increased in vitrified oocytes, which was recovered by Ax treatment. The mitochondrial activity did not differ between fresh and vitrified oocytes, and was significantly enhanced in Ax-treated oocytes. Furthermore, Ax significantly restored the decreased expression of BMP15, ZAR1, POU5F1, GPX4 and LAMP2 genes in vitrified oocytes. Both fresh and vitrified oocytes treated with Ax showed significantly higher mRNA levels of GDF9, POU5F1, SOD2, NRF2 and ATG5. Taken together, this study provides new perspectives in understanding the mechanisms by which Ax improves the developmental competence of both fresh and vitrified porcine oocytes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vitrificação / Antioxidantes Limite: Animals Idioma: En Revista: Theriogenology Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vitrificação / Antioxidantes Limite: Animals Idioma: En Revista: Theriogenology Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China