Reduction of embryotoxicity by protein in embryo culture media

Abstract

Experiments tested the hypothesis that one role of protein in embryo culture media is protection of embryos against potentially embryotoxic substances in the media. Mouse embryos were cultured in modified Krebs–Ringer bicarbonate medium and in modified Tyrode's medium, aliquots of which were supplemented with 4 mg/ml of the protein bovine serum albumin (BSA), while other aliquots were left protein free. The media were prepared using water samples that differed in purity, as reflected by differences in conductivity, with tap water being least pure (and considered to have the greatest potential for being embryotoxic) and water that had been purified by reverse osmosis, Milli‐Q filtration, and triple distillation being most pure. Embryos were placed in the media while in the two‐cell stage of development and their development was assessed after 24, 48, and 72 hr of culture. Rate of embryo development in BSA‐supplemented media was greater than that in protein‐free media only when the media was greater than that in protein‐free media only when the media were prepared with the least purified water samples. Because these water samples would have contained substances not contained in media prepared with purer water, or would have contained the substances in higher concentrations, the data supported the hypothesis that protein can protect embryos during culture by negating effects of embryotoxic substances in the media.