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Effect of retinol as antioxidant on the post-thaw viability and the expression of apoptosis and developmental competence-related genes of vitrified preantral follicles in buffalo (Bubalus bubalis).
Gupta, Psp; Johnson, P; Kaushik, K; Krishna, K; Nandi, S; Mondal, S; Nikhil Kumar Tej, J; Somoskoi, B; Cseh, S.
Afiliação
  • Gupta P; ICAR-National Institute of Animal Nutrition and Physiology, Bengaluru, India.
  • Johnson P; ICAR-National Institute of Animal Nutrition and Physiology, Bengaluru, India.
  • Kaushik K; ICAR-National Institute of Animal Nutrition and Physiology, Bengaluru, India.
  • Krishna K; ICAR-National Institute of Animal Nutrition and Physiology, Bengaluru, India.
  • Nandi S; ICAR-National Institute of Animal Nutrition and Physiology, Bengaluru, India.
  • Mondal S; ICAR-National Institute of Animal Nutrition and Physiology, Bengaluru, India.
  • Nikhil Kumar Tej J; ICAR-National Institute of Animal Nutrition and Physiology, Bengaluru, India.
  • Somoskoi B; Department and Clinic of Obstetrics & Reproduction, University of Veterinary Medicine, Budapest, Hungary.
  • Cseh S; Department and Clinic of Obstetrics & Reproduction, University of Veterinary Medicine, Budapest, Hungary.
Reprod Domest Anim ; 56(11): 1446-1455, 2021 Nov.
Article em En | MEDLINE | ID: mdl-34449946
ABSTRACT
The present study evaluated the effect of supplementation of retinol in the vitrification solution on the viability, apoptosis and development-related gene expression in vitrified buffalo preantral follicles. Preantral follicles isolated from cortical slices of ovaries were randomly assigned into three groups Group1-Control fresh preantral follicles; Group 2-Vitrification treatment (Vitrification solution 1 (VS1) -TCM-199 + 25 mM HEPES + Foetal bovine serum (FBS) 10%, Ethylene glycol (EG) 10%, Dimethyl sulphoxide (DMSO) 10%, Sucrose-0.3 M for 4 min; VS2- TCM-199 + 25 mM HEPES + FBS10%, EG25%, DMSO 25%, Sucrose0.3 M for 45 s); Group3-vitrification treatment +5 µM of Retinol. Preantral follicles were placed in corresponding vitrification medium and plunged into liquid nitrogen (-196°C). After a week, the follicles were thawed and analysed for follicular viability and gene expression. There was no significant difference in the viability rates among the Group 1(Fresh preantral follicles) (91.46 ± 2.39%), Group 2 (89.59 ± 2.46%) and Group 3 (87.19 ± 4.05%). There was a significantly (p < .05) higher mRNA expression of BCL2L1, GDF-9 and BMP-15 in the vitrification + retinol group compared with the control group. There was a significantly (p < .05) higher expression of Caspase-3 and Annexin-5 in the vitrification group and Vitrification + retinol group compared with control group of follicles. It is concluded that the supplementation of 5 µM of Retinol in Vitrification solution was an efficient vitrification procedure for the vitrification of buffalo preantral follicles.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vitamina A / Criopreservação / Folículo Ovariano / Antioxidantes Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vitamina A / Criopreservação / Folículo Ovariano / Antioxidantes Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article