Loading…

Donor and recipient rat strains affect full-term development of one-cell zygotes cultured to morulae/blastocysts

The present study was conducted to examine the developmental potential to offspring of rat embryos cultured from 1-cell to morula/blastocyst stage. Pronuclear zygotes from Wistar * Wistar or (SD * DA) * Wistar strains were cultured in modified rat 1-cell embryo culture medium (mR1ECM) for 96 h in 5%...

Full description

Saved in:
Bibliographic Details
Published in:Journal of Reproduction and Development 2004, Vol.50(2), pp.191-195
Main Authors: Kato, M. (National Inst. for Physiological Sciences, Okazaki, Aichi (Japan)), Ishikawa, A, Hochi, S, Hirabayashi, M
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The present study was conducted to examine the developmental potential to offspring of rat embryos cultured from 1-cell to morula/blastocyst stage. Pronuclear zygotes from Wistar * Wistar or (SD * DA) * Wistar strains were cultured in modified rat 1-cell embryo culture medium (mR1ECM) for 96 h in 5% C02 in air at 37 C. The proportion of the 3-way cross hybrid zygotes developing into morula/blastocyst stage (74%) was higher than that of the Wistar zygotes (66%). Day-5 morulae/ blastocysts developed in vitro were transferred into Day-3 or -4 pseudopregnant recipients of Wistar or SD * DA strain. The transfer of cultured embryos resulted in the birth of offspring at 13-59%, while that of non-cultured control blastocysts showed birth rates of 35-65%. The best offspring rate of cultured embryos (59%) was obtained when the hybrid 1-cell zygotes were cultured in mR1ECM medium and transferred into the 2-days earlier uteri of SD * DA recipients. These results suggest that genetic background of recipients as well as donors is a possible factor affecting full-term development of rat morulae/blastocysts derived from 1-cell stage zygotes cultured in vitro.
ISSN:0916-8818
1348-4400
DOI:10.1262/jrd.50.191