Fertility and Sterility
Volume 90, Issue 4, Supplement , Pages 1503-1510, October 2008

Comparison of the efficacy of two commercially available media for culturing one-cell embryos in the in vitro fertilization mouse model

  • Paulo Marcelo Perin, M.D.

      Affiliations

    • Department of Pathology, University of São Paulo School of Medicine, São Paulo, Brazil
    • Division of Reproductive Medicine, CEERH, Specialized Center for Human Reproduction, São Paulo, Brazil
    • Corresponding Author InformationReprint requests: Paulo Marcelo Perin, M.D., Division of Reproductive Medicine, CEERH–Specialized Center for Human Reproduction, R. Pará, n. 50, 12th floor, São Paulo 01243-0020, Brazil (FAX: 55-11-3258-0008).
  • ,
  • Mariangela Maluf, M.D.

      Affiliations

    • Department of Pathology, University of São Paulo School of Medicine, São Paulo, Brazil
    • Division of Reproductive Medicine, CEERH, Specialized Center for Human Reproduction, São Paulo, Brazil
  • ,
  • Daniela Aparecida Nicolosi Foltran Januário, B.Sc.

      Affiliations

    • Department of Experimental Physiopathology, University of São Paulo School of Medicine, São Paulo, Brazil
    • Division of Reproductive Medicine, CEERH, Specialized Center for Human Reproduction, São Paulo, Brazil
  • ,
  • Paulo Hilário Nascimento Saldiva, M.D., Ph.D.

      Affiliations

    • Department of Pathology, University of São Paulo School of Medicine, São Paulo, Brazil

Received 23 March 2007; received in revised form 29 September 2007; accepted 29 September 2007. published online 28 January 2008.

Objective

To examine the effects of two commercial media on the development of mouse ova fertilized in vitro to the blastocyst stage.

Design

Animal model.

Setting

Academic institution.

Animal(s)

Eight-week old, superovulated mice.

Intervention(s)

One-cell embryos cultured in vitro up to the blastocyst stage in potassium-enriched simplex optimized medium (KSOM) or G1/G2 medium.

Main Outcome Measure(s)

Blastocyst and hatching rates, total cell number count, and proportion of allocation of cells to the inner cell mass (ICM) and trophectoderm (TE).

Result(s)

The percentage of zygotes that developed to the blastocyst stage 96 and 120 hours after insemination was statistically significantly higher in the KSOM group. The percentage of blastocysts that partially or completely hatched by day 5 of culture was 84% and 71% for the KSOM and G1/G2 groups, respectively, showing a statistically significant difference between the groups. The mean number of ICM cells was 11.7 ± 4.0 and 9.2 ± 5.2 for the zygotes cultured in KSOM and G1/G2 media, respectively, revealing a statistically significantly higher cell number in the ICM of blastocysts derived from culture in KSOM medium. The ICM/TE ratio in the blastocysts cultured in KSOM or G1/G2 media was similar in both groups.

Conclusion(s)

Commercially available KSOM medium is superior to sequential G1/G2 media for culturing one-cell embryos up to the blastocyst stage in the mouse IVF model.

Key Words: Mouse, in vitro fertilization, embryo culture, blastocyst, animal model

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PII: S0015-0282(07)03758-2

doi:10.1016/j.fertnstert.2007.09.062

Fertility and Sterility
Volume 90, Issue 4, Supplement , Pages 1503-1510, October 2008