Premium
Effects of metabolic inhibitors on mouse preimplantation embryo development and the energy metabolism of isolated inner cell masses
Author(s) -
Hewitson Laura C.,
Martin Karen L.,
Leese Henry J.
Publication year - 1996
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/(sici)1098-2795(199603)43:3<323::aid-mrd6>3.0.co;2-s
Subject(s) - biology , embryo , metabolism , transamination , biochemistry , cell , carbohydrate metabolism , embryogenesis , inner cell mass , blastocyst , microbiology and biotechnology , amino acid
Abstract The effects of two metabolic inhibitors, methyl palmoxirate (MP) and amino‐oxyacetate (AOA), on mouse preimplantation embryo development and cell number, and inner cell mass (ICM) cell metabolism have been examined. Two‐cell embryos were cultured in media supplemented with either MP, which inhibits fatty acid oxidation, or AOA, which inhibits the transamination of glutamate into α‐ketoglutarate. Embryos were scored for development daily. On day 5, expanded blastocysts were differentially labeled with fluorochromes to visualize TE and ICM cell nuclei, or the ICMs isolated by immunosurgery and their energy metabolism determined using microfluorometric methods. Embryos exposed to the two inhibitors developed into fully expanded blastocysts, although cell numbers of both the TE and ICM cells were significantly reduced compared to controls. The uptake of glucose in the presence of 1 mM MP or AOA did not differ from the controls, but less glucose was accountable for by lactate production. MP significantly reduced lactate production. In the presence of 4 mM AOA, the amount of glucose oxidized and the amount of lactate formed by ICMs were significantly reduced. The results indicate that the fuels used by isolated mouse ICMs vary in response to substrate availability and that fatty acids may be a potential energy source. © 1996 Wiley‐Liss, Inc.