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Vertebrate reproductive science and technology
RESEARCH ARTICLE

Osmotic stress induced by sodium chloride, sucrose or trehalose improves cryotolerance and developmental competence of porcine oocytes

Lin Lin A C D G , Peter M. Kragh A C , Stig Purup B , Masashige Kuwayama E , Yutao Du A C D , Xiuqing Zhang D , Huanming Yang D , Lars Bolund C , Henrik Callesen A and Gábor Vajta F
+ Author Affiliations
- Author Affiliations

A Population Genetics and Embryology, Department of Genetics and Biotechnology, Faculty of Agricultural Sciences, University of Aarhus, DK-8830 Tjele, Denmark.

B Nutrition and Production Physiology, Department of Animal Health, Welfare and Nutrition, Faculty of Agricultural Sciences, University of Aarhus, DK-8830 Tjele, Denmark.

C Institute of Human Genetics, University of Aarhus, DK-8000 Aarhus, Denmark.

D Beijing Genomics Institute, Airport-Industrial Zone B-6, Beijing 101300, China.

E Kato Ladies’ Clinic, Nishishinjuku, Shinjuku, Tokyo 160-0023, Japan.

F PIVET Medical Centre, 166–168 Cambridge Street, Perth, WA 6007, Australia.

G Corresponding author. Email: lin.lin@agrsci.dk

Reproduction, Fertility and Development 21(2) 338-344 https://doi.org/10.1071/RD08145
Submitted: 24 June 2008  Accepted: 29 September 2008   Published: 27 January 2009

Abstract

Exposure of porcine oocytes to increased concentrations of NaCl prior to manipulation has been reported not only to increase cryotolerance after vitrification, but also to improve developmental competence after somatic cell nuclear transfer (SCNT). In the present study we compared the effects of NaCl with those of concentrated solutions of two non-permeable osmotic agents, namely sucrose and trehalose, on the cryotolerance and developmental competence of porcine oocytes. In Experiment 1, porcine in vitro-matured cumulus–oocyte complexes (COCs; n = 1200) were exposed to 588 mOsmol NaCl, sucrose or trehalose solutions for 1 h, allowed to recover for a further 1 h, vitrified, warmed and subjected to parthenogenetic activation. Both Day 2 (where Day 0 is the day of activation) cleavage and Day 7 blastocyst rates were significantly increased after NaCl, sucrose and trehalose osmotic treatments compared with untreated controls (cleavage: 46 ± 5%, 44 ± 7%, 45 ± 4% and 26 ± 6%, respectively; expanded blastocyst rate: 6 ± 1%, 6 ± 2%, 7 ± 2% and 1 ± 1%, respectively). In Experiment 2, COCs (n = 2000) were treated with 588 mOsmol NaCl, sucrose or trehalose, then used as recipients for SCNT (Day 0). Cleavage rates on Day 1 did not differ between the NaCl-, sucrose-, trehalose-treated and the untreated control groups (92 ± 3%, 95 ± 3%, 92 ± 2% and 94 ± 2%, respectively), but blastocyst rates on Day 6 were higher in all treated groups compared with control (64 ± 2%, 69 ± 5%, 65 ± 3% and 47 ± 4%, respectively). Cell numbers of Day 6 blastocysts were higher in the control and NaCl-treated groups compared with the sucrose- and trehalose-treated groups. In conclusion, treatment of porcine oocytes with osmotic stress improved developmental competence after vitrification combined with parthenogenetic activation, as well as after SCNT.

Additional keywords: hand-made cloning, parthenogenetic activation, vitrification.


Acknowledgements

The authors thank John Yovich for professional and language corrections and suggestions, and Klaus Villemoes, Anette Pedersen, Janne Adamsen and Ruth Kristensen for their excellent technical support.


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