DMSO supplementation during in vitro maturation of bovine oocytes improves blastocyst rate and quality

被引:13
|
作者
Eugenia Ynsaurralde-Rivolta, Amada [1 ,2 ]
Suva, Mariana [1 ]
Griselda Luchetti, Carolina [3 ,4 ]
Jimena Bevacqua, Romina [1 ,5 ]
Munilla, Sebastian [4 ,5 ]
Rodriguez-Alvarez, Lleretny [6 ]
Velasquez, Alejandra [6 ]
Briski, Olinda [1 ,4 ,5 ]
Lombardo, Daniel [3 ]
Salamone, Daniel [1 ,4 ,5 ]
机构
[1] Buenos Aires Univ, Fac Agron, Anim Biotechnol Lab, INPA CONICET, Buenos Aires, DF, Argentina
[2] INTA, Estn Expt Agr Mercedes, Corrientes, Argentina
[3] Univ Buenos Aires, Fac Ciencias Vet, Inst Invest & Tecnol Reprod Anim INITRA, Catedra Histol & Embriol, Buenos Aires, DF, Argentina
[4] Consejo Nacl Invest Cient & Tecn, Buenos Aires, DF, Argentina
[5] Univ Buenos Aires, Fac Agron, Dept Prod Anim, Buenos Aires, DF, Argentina
[6] Univ Concepcion, Fac Ciencias Vet, Chillan, Chile
关键词
Cattle; Embryo; Oxidative stress; HYDROXYL RADICAL SCAVENGERS; DIMETHYL-SULFOXIDE; EMBRYO DEVELOPMENT; DEVELOPMENTAL COMPETENCE; PREIMPLANTATION EMBRYOS; OXIDATIVE STRESS; GLUTATHIONE; CULTURE; OXYGEN; DIMETHYLSULFOXIDE;
D O I
10.1016/j.theriogenology.2020.02.045
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The molecule Dimethyl sulfoxide is widely used as drug solvent. However, its antioxidant property was poorly explored. In this study, we evaluated the effect of DMSO supplementation during oocyte in vitro maturation (IVM) on embryo development and quality. Bovine oocytes were matured with different DMSO concentrations (0, 0.1, 0.25, 0.5, 0.75,1 and 10% v:v) followed by in vitro fertilization. Subsequently, quality indicators such as gene expression of SOX2, OCT4, CDX2, SOD1, oocyte and embryo redox status and DNA damage were evaluated. Polar body extrusion and blastocyst rates increased with 0.5% v:v DMSO. Moreover, first polar body extrusion and blastocyst rates did not increase with 1%, and 10% of DMSO reduced polar body extrusion and did not produce blastocyst. Optimal concentration of DMSO for the use on the maturation was estimated at around 0.45% v:v. Supplementation with 0.5% v:v DMSO has not affected mRNA abundance of genes key in blastocyst, however 0.75% increased gene expression of OCT4 and SOX2. Oocytes matured with 0.5% v:v DMSO and blastocyst from DMSO group showed reduced lipid peroxidation respect control. Total Glutathione concentrations increased in blastocyst stage in DMSO group. DMSO increased the total cell number of blastocysts but not TUNEL positive cells. In conclusion, our results suggest that low DMSO concentrations used during bovine oocytes in vitro maturation increases the maturation, as well as the blastocyst rate and its quality, without demonstrating deleterious effect on embryo cells. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:140 / 148
页数:9
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