Effect of osmotic stress on the developmental competence of germinal vesicle and metaphase II stage bovine cumulus oocyte complexes and its relevance to cryopreservation
✍ Scribed by Y. Agca; J. Liu; J.J. Rutledge; E.S. Critser; J.K. Critser
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 143 KB
- Volume
- 55
- Category
- Article
- ISSN
- 1040-452X
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✦ Synopsis
The effects of osmotic stress on germinal vesicle (GV) and metaphase II (MII) stage bovine cumulus oocyte complexes (COCs) were evaluated by first exposing them to various anisotonic NaCl solutions (75, 150, 600, 1200, 2400, and 4800 Ϯ 5 mOsm/kg) for 10 min and then returning them to isotonic TL-Hepes solution (270 Ϯ 5 mOsm/kg) at 20 Ϯ 2ЊC. Percentages of oocyte maturation, fertilization, polyspermy, cleavage, and blastocyst formation were measured as endpoints. Exposure to anisotonic conditions had a significant (P Ͻ 0.05) effect on the developmental competence of both GV and bovine MII COCs. Oocytes at the GV stage were more sensitive to anisotonic stress than MII oocytes (P Ͻ 0.05). None of the GV oocytes developed to the blastocyst stage after exposure to hypertonic conditions (2400 or 4800 mOsm solutions), while exposure to hypotonic conditions (75 or 150 mOsm solutions) resulted in significantly lower (P Ͻ 0.05) blastocyst formation (9% and 13%, respectively) compared to the isotonic control (25%). A dramatic decrease to 4% development to blastocyst was observed for MII oocytes following exposure to a 4800 mOsm solution. Blastocyst formation of MII oocytes which were exposed to 75, 150, 600, 1200, or 2400 mOsm solutions were similar (15%, 20%, 18%, 14%, and 13%, respectively; P Ͼ 0.05), but lower (P Ͻ 0.05) than those in the control group (29%). Exposing GV oocytes to anisotonic conditions increased polyspermic fertilization (P Ͻ 0.05), although MII oocytes were not similarly affected (P Ͼ 0.05). These data support the hypothesis that osmotic stress is detrimental to bovine oocytes and must be considered when developing optimized cryopreservation procedures for these cells.