Evaluation of Cryopreservation of Bovine Ovarian Tissue by Analysis of Reactive Species of Oxygen, Toxicity, Morphometry, and Morphology DOI Creative Commons
Camila Bizarro‐Silva, Larissa Zamparone Bergamo, Camila Bortoliero Costa

et al.

Veterinary Sciences, Journal Year: 2024, Volume and Issue: 11(11), P. 579 - 579

Published: Nov. 19, 2024

Ovarian tissue cryopreservation has been widely investigated for preserving female fertility. In the present study, we aimed to compare effects of three concentrations (1, 1.5, and 3 M) dimethylsulfoxide (DMSO) on vitrification ovarian tissue. The cortex was divided into control vitrified groups: (i) 1 M-DMSO, (ii) 1.5 (iii) M-DMSO. Follicles from all fragments were analyzed DMSO-induced deleterious effects, morphological morphometric aspects, concentration reactive oxygen species. Additionally, cultured assess integrity return follicular development post-vitrification. All DMSO resulted in a higher percentage degenerated preantral follicles than before process. After vitrification, cryopreserved showed similar percentages intact follicles; however, M differed control. Analyzing free radical production, found that had levels oxidative stress lower DMSO. vitro cultivation vitrified/warmed fragments, exhibited morphologically other concentrations. Therefore, suggest bovine can be situ with greater efficiency

Language: Английский

Técnicas in vivo e in vitro sobre calidad y viabilidad de embriones en bovinos DOI Creative Commons

Denisse Maryeli Loor Loor,

Jorge Ignacio Macías Andrade

Revista Científica Arbitrada Multidisciplinaria PENTACIENCIAS, Journal Year: 2025, Volume and Issue: 7(1), P. 274 - 282

Published: Jan. 17, 2025

En las últimas décadas, la producción de embriones in vivo e vitro han revolucionado ganadería, lo que permitió obtener avances mejoramiento genético, que, en efecto, dichas técnicas se llevaron a cabo otras especies zootécnicas. Ambas son fundamentales para evaluar calidad y viabilidad bovinos, técnica vivo, da cuatro fases el tracto reproductivo vaca, cuales son; superestimulación, inseminación, desarrollo, recolección. A diferencia recolectan los ovocitos posterior ello, requiere instalaciones laboratorio llevar maduración, fertilización cultivo. El presente artículo tiene sustentó teórico diversas bases datos científicas, así como gestión selección documentos clave. Se espera resultados esta investigación proporcionen información sólida sobre diferencias bovinos manera, permitan conocer ventajas desventajas biotecnologías programas reproducción asistida.

Citations

0

Effects of Different Cryoprotectants on Cryopreservation of Sperm from Noble Scallop Mimachlamys nobilis DOI Creative Commons
Minghao Li, Zhengyi Fu, Gang Yu

et al.

Journal of Marine Science and Engineering, Journal Year: 2025, Volume and Issue: 13(3), P. 607 - 607

Published: March 19, 2025

In cryopreservation technology, the choice of cryoprotectant plays a crucial role in cell survival and function. Different types cryoprotectants, each with unique protective mechanisms, mitigate cellular damage from ice crystal formation during freezing. This study investigated effects different concentrations cryoprotectants on efficacy noble scallop Mimachlamys nobilis sperm. Six were tested, including four permeable (dimethyl sulfoxide (DMSO), ethylene glycerol (EG), propylene (PG), methanol (MET)) two non-permeable (trehalose (TRE), fetal bovine serum (FBS)). The results showed that which penetrate membrane, regulate osmotic pressure inside outside cells to reduce dehydration damage. Among them, 10% DMSO provided best protection, significantly preserving sperm motility, velocity, morphology. Non-permeable although unable cells, stabilized extracellular environment at higher (such as FBS). Additionally, MET FBS exhibited enhanced increasing concentration, indicating their potential reducing structural concentrations. Morphological observations indicated freezing caused varying degrees sperm, flagellar integrity being for motility. Overall, selecting an appropriate concentration is essential efficient M. providing valuable reference conserving germplasm resources marine species.

Language: Английский

Citations

0

Transparent Alumina Ceramics‐Based Microfluidic Chip Enables on‐Chip Cryopreservation for Mouse Oocyte DOI Open Access

Siyu Xu,

Lei Yu,

Morgan K Wei

et al.

Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown

Published: March 20, 2025

Abstract Oocyte cryopreservation plays a crucial role in safeguarding female fertility clinical practice. However, commonly used methods involving tedious and time‐consuming procedures, as well uncontrolled variability between operators, which can easily lead to cell damage. Here, novel method for cryopreserving oocytes using transparent alumina ceramics‐based microfluidic chip is developed, provides an integrated platform cryoprotectants (CPAs) loading/unloading, freeze‐thaw process storage. The protocol optimized significantly simplify the overall process, reduce CPA osmotic damage, achieve high‐performance oocyte cryopreservation. survival rate of cryopreserved with this reached 86.23%. In comparison conventional method, recovered exhibit structural stability, functional integrity, genetic normality higher developmental capacity. study offers low‐cost, easy‐to‐operate, high‐performance, on‐chip semi‐automatic technique oocytes, great significance standardizing automating fertility, has important potential translational applications.

Language: Английский

Citations

0

Evaluation of Cryopreservation of Bovine Ovarian Tissue by Analysis of Reactive Species of Oxygen, Toxicity, Morphometry, and Morphology DOI Creative Commons
Camila Bizarro‐Silva, Larissa Zamparone Bergamo, Camila Bortoliero Costa

et al.

Veterinary Sciences, Journal Year: 2024, Volume and Issue: 11(11), P. 579 - 579

Published: Nov. 19, 2024

Ovarian tissue cryopreservation has been widely investigated for preserving female fertility. In the present study, we aimed to compare effects of three concentrations (1, 1.5, and 3 M) dimethylsulfoxide (DMSO) on vitrification ovarian tissue. The cortex was divided into control vitrified groups: (i) 1 M-DMSO, (ii) 1.5 (iii) M-DMSO. Follicles from all fragments were analyzed DMSO-induced deleterious effects, morphological morphometric aspects, concentration reactive oxygen species. Additionally, cultured assess integrity return follicular development post-vitrification. All DMSO resulted in a higher percentage degenerated preantral follicles than before process. After vitrification, cryopreserved showed similar percentages intact follicles; however, M differed control. Analyzing free radical production, found that had levels oxidative stress lower DMSO. vitro cultivation vitrified/warmed fragments, exhibited morphologically other concentrations. Therefore, suggest bovine can be situ with greater efficiency

Language: Английский

Citations

0