Maintenance of developmental competence in feline oocytes following 24 h of meiotic arrest with physiological agents

Context In vitro matured (IVM) feline oocytes exhibit reduced developmental competence compared to in vivo matured oocytes. Aims Arresting meiosis prior to IVM (pre-IVM) has been shown to improve oocyte quality in other species. Methods Cumulus-oocyte complexes (COCs) from domestic cats were matured in vitro immediately after collection or following 24h of pre-IVM. Following IVF, embryonic development was evaluated. Key results Embryonic cleavage, development to blastocyst, and hatching were not different (P >0.05) for oocytes subjected to meiotic arrest compared to control oocytes. Gene expression of pluripotency markers and blastocyst cell numbers were also unchanged by the various pre-IVM supplements. Conclusions It is possible to maintain feline oocytes in culture for up to 24h without compromising developmental competence. Implications Further manipulation of the culture environment during this period of meiotic arrest could be a novel means of improving the quality of feline oocytes.

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Publication Details

Journal
Reproduction Fertility and Development
Published
2025-06-16
DOI
https://doi.org/10.1071/rd25049
Primary Topic
Reproductive Biology and Fertility
Type
article
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article

Maintenance of developmental competence in feline oocytes following 24 h of meiotic arrest with physiological agents

Shelley E. S. Sandmaier, Jason R. Herrick
2 links
Reproduction Fertility and Development
Reproductive Biology and Fertility
article

Maintenance of developmental competence in feline oocytes following 24 h of meiotic arrest with physiological agents

Shelley E. S. Sandmaier, Jason R. Herrick
article en

Abstract

Context In vitro matured (IVM) feline oocytes exhibit reduced developmental competence compared to in vivo matured oocytes. Aims Arresting meiosis prior to IVM (pre-IVM) has been shown to improve oocyte quality in other species. Methods Cumulus-oocyte complexes (COCs) from domestic cats were matured in vitro immediately after collection or following 24h of pre-IVM. Following IVF, embryonic development was evaluated. Key results Embryonic cleavage, development to blastocyst, and hatching were not different (P >0.05) for oocytes subjected to meiotic arrest compared to control oocytes. Gene expression of pluripotency markers and blastocyst cell numbers were also unchanged by the various pre-IVM supplements. Conclusions It is possible to maintain feline oocytes in culture for up to 24h without compromising developmental competence. Implications Further manipulation of the culture environment during this period of meiotic arrest could be a novel means of improving the quality of feline oocytes.

Reproduction Fertility and DevelopmentVol. 37(10)
Zoological Society of San Diego (US), Columbus Zoo and Aquarium (US), Retina Foundation of the Southwest (US), San Diego Zoo Institute for Conservation Research (US), Centre for Conservation and Research (LK)
Zero hunger
Openalex Percentile: Top 81%
Reproductive Biology and Fertility
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Maintenance of developmental competence in feline oocytes following 24 h of meiotic arrest with physiological agents — Shelley E. S. Sandmaier, Jason R. Herrick · Reproduction Fertility and Development (2025) | TGRS Research Map | TGRS