Effect of supplementation of cryoprotectant solution with hydroxypropyl cellulose for vitrification of bovine oocytes

• Published in: Cryo-Letters Vol. 44; no. 1; p. 37
• Main Authors: Park, M J, Lee, S E, Yoon, W, Park, H J, Kim, S H, Oh, S H, Lee, D G, Pyeon, D B, Kim, E Y, Park, S P
• Format: Journal Article
• Language: English
• Published: England 01-01-2023
• Subjects: Animals; Cattle; Cryopreservation - veterinary; Cryoprotective Agents - pharmacology; Dietary Supplements; Ethylene Glycols - pharmacology; Oocytes - physiology; Vitrification
• ISSN: 0143-2044
• DOI: 10.54680/fr23110110212

Successful cryopreservation of bovine oocytes is very important for research and commercial applications. However, the survival and development rate of vitrified-thawed (VT) oocytes are lower than those of non-vitrified-thawed (non-VT) oocytes.
To investigate the effect of adding hydroxypropyl cellulose (HPC) to the vitrification solution for bovine oocytes.
For vitrification, bovine metaphase II oocytes were pretreated with a solution containing 10% ethylene glycol supplemented with 0, 10, 50, or 100 ug/mL HPC for 5 min, exposed to a solution containing 30% ethylene glycol supplemented with 0, 10, 50, or 100 ug/mL HPC for 30 s, and then directly plunged into liquid nitrogen.
The survival rate of oocytes was significantly higher in the 50 HPC group than in the 0, 10, and 100 HPC groups. The reactive oxygen species level was lower in the non-VT and 50 HPC groups than in the other groups. The mRNA levels of proapoptotic genes (Bax) were lower in the non-VT, 0, and 50 HPC groups than in the other groups. The mRNA levels of antiapoptotic genes (BCl2) were higher in the non-VT than in the other groups. The development rates of embryos (day 8) obtained via parthenogenetic activation (PA) were determined in the non-VT, 0 HPC, and 50 HPC groups. The cleavage rate was significantly higher in the non-VT group.
Supplementation of vitrification solution with HPC improves the survival of VT bovine oocytes and the development capacity of embryos derived from these oocytes via PA. doi.org/10.54680/fr23110110212.