AI Article Synopsis

  • The study examined how relaxin and IGF-I affect blastocyst development in Mongolian gerbils' embryos during early stages of implantation.
  • Both relaxin and IGF-I increased cell numbers in blastocysts, with relaxin showing a more significant effect on development and protein synthesis compared to controls.
  • The findings suggest that these factors could enhance embryonic development and protein production in vitro, which may have implications for reproductive biology research.

Article Abstract

Purpose: Both relaxin and insulin-like growth factor (IGF) are members of the insulin super family. This study aimed to investigate the effect of relaxin and IGF-I on the pre-implantation of Mongolian gerbil of blastocyst development in vitro.

Methods: Blastocysts and eight-cell stage embryos were collected from female gerbils. Eight-cell embryos and blastocysts were cultured in mM16 medium supplemented with or without relaxin or IGF-I for 24 h. Blastocysts were counted for total, inner cell mass (ICM) and trophectoderm (TE) cell numbers, and assessed apoptosis incidence. In addition, to measure incorporation of H-methionine, blastocysts were cultured for 3 h with relaxin or IGF-I, washed with trichloroacetic acid and measured by liquid scintiration counter.

Results: Relaxin (200 ng/ml) increased total, TE and ICM cell numbers of blastocyst ( < 0.05) when it was compared with the control. IGF-I (150 ng/ml) also has influence on total and ICM cell numbers of blastocyst when compared with control. Apoptosis incidence was relatively low, and a significant difference was not observed between each group. The effect of relaxin on incorporation of H-methionine was higher than the control group ( < 0.05). Relaxin increased the developmental rate from the eight-cell stage to blastocyst ( < 0.05).

Conclusions: In conclusion, relaxin and IGF-I stimulated protein synthesis and increased cell numbers of blastocysts, promoting development of the gerbil embryo in vitro culture.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906978PMC
http://dx.doi.org/10.1007/s12522-008-0007-4DOI Listing

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