Effect of exposure duration of ovaries and oocytes at ambient temperature on parthenogenetic development of porcine follicular oocytes

• Published in: Journal of Reproduction and Development Vol. 52; no. 5; pp. 633 - 638
• Main Authors: Kim, H.J.(National Livestock Research Inst., Namwon (Korea R.)), Choi, S.H, Son, D.S, Cho, S.R, Choe, C.Y, Kim, Y.K, Han, M.H, Ryu, I.S, Kim, I.C, Kim, I.H, Im, K.S, Nagai, T
• Format: Journal Article
• Language: English
• Published: Japan THE SOCIETY FOR REPRODUCTION AND DEVELOPMENT 01.10.2006
• Subjects: AIR TEMPERATURE; Animals; CERDO; CULTIVO IN VITRO; CULTURE IN VITRO; DEVELOPMENTAL STAGES; ETAPAS DE DESARROLLO; Female; Follicular Fluid; IN VITRO CULTURE; Oocyte; Oocytes - growth & development; OVA; OVAIRE; OVARIES; OVARIOS; Ovary; Ovary - physiology; OVULE; OVULO; PARTENOGENESIS; PARTHENOGENESE; PARTHENOGENESIS; Parthenogenesis - physiology; Parthenogenetic activation; PORCIN; Porcine; STADE DE DEVELOPPEMENT; SWINE; TEMPERATURA DEL AIRE; Temperature; TEMPERATURE DE L'AIR; Time Factors
• ISSN: 0916-8818; 1348-4400
• DOI: 10.1262/jrd.17103

This study was conducted to evaluate the effects of exposing porcine ovaries to 30-33 C during transportation for 4 h and subsequently room temperature (25 C) for 6 h of storage on in vitro maturation (IVM) and subsequent parthenogenetic development of oocytes collected from the ovaries. After IVM, oocytes having a tight oopalsm membrane and no signs of degeneration were exposed to Dulbecco's phosphate-buffered saline (DPBS) with 7% ethanol (v/v) for 7 min to induce parthenogenetic activation. Moreover, we also determined whether exposure of the collected oocytes to room temperature for 1, 2 and 4 h in DPBS or porcine follicular fluid (pFF) affected parthenogenetic development. When porcine ovaries were stored after transportation, oocytes collected from the stored ovaries showed a significantly higher rate of degeneration after 65 h of IVM (58.4%) and a significantly lower rate of cleavage after parthenogenetic activation (40.1%) than oocytes collected from ovaries immediately after transportation (38.9% and 47.4%, respectively). However, there was no significant difference in developmental rates to the morula and blastocyst stages between these two groups (14.4% and 14.3%, respectively). The duration of preservation, 1, 2, and 4 h, of oocytes in DPBS did not affect parthenogenetic development. In contrast, when preserved for 4 h in pFF, the developmental rates of the oocytes were significantly decreased. This suggested that some factor(s) in follicular fluid affects the developmental rate of oocytes with the passage of time in ambient conditions. These results suggest that even after 6 h storage of ovaries, oocytes having normal morphology after IVM have the same rate of parthenogenetic development as oocytes collected from ovaries just after 4 h of transportation, except for a lower cleavage rate, and that exposure of oocytes to room temperature for 4 h in DPBS does not affect their parthenogenetic developmental competence.