2A). When relative area was compared Selleckchem Vemurafenib between different stages, embryos at expanded blastocyst stage underwent higher (P < 0.05) reduction in area at T5 than embryos at blastocyst stage. However, area recovery was greater (P < 0.05) for embryos at blastocyst stage at T10 and T120 ( Fig. 2B). Expression of ATPase1 and Aqp3 genes was compared between embryos with greater (1.18 ± 0.02; n = 15) and lower (0.82 ± 0.03; n = 15) area recovery after 5 min in hypertonic medium

followed by 120 min in isotonic medium ( Fig. 3) in order to detect an association between level of rehydration and gene expression. No difference (P > 0.05) on relative abundance of ATPase1 and Aqp3 transcripts between embryos with high and low rehydration was found ( Fig. 4A). Viability of vitrified-warmed embryos and relative abundance of ATPase1 and Aqp3 transcripts were evaluated after culturing embryos for 72 h. Embryos survival was lower (P < 0.05) following vitrification (57.9%; n = 57) than for fresh (non-vitrified) embryos

Pifithrin-�� cell line (84.6%; n = 52). The relative abundance of Aqp3 was lower (P < 0.01) for vitrified-warmed embryos, but no difference (P > 0.05) on ATPase1 was found ( Fig. 4B). Membrane permeability is crucial for cell survival during cryopreservation. The current study shows that culture medium can influence the ability of in vitro fertilized bovine embryos to undergo shrinkage and swelling. Such ability can also be influenced by embryo stage. In addition, it shows that the embryo rehydrating ability after exposure to a NaCl hypertonic medium is not associated with the expression of Aqp3 Casein kinase 1 and ATPase1 genes; the amount of Aqp3 transcripts, however, can be altered following a vitrification/warming procedure. CR2aa and SOFaac are media commonly used for culture of in vitro-fertilized bovine embryos [32], [14], [27] and [6] and both produce similar embryos rates. The present study used these media in the co-culture system and also observed no difference on embryo production. Embryo ability to undergo dehydration, however, was affected by these different culture media, with higher dehydration

being found for embryos cultured in SOFaac medium. These finding suggest that embryos co-cultured in SOFaac medium may have greater permeability to water when exposed to hypertonic solutions. We showed that embryos at expanded blastocyst stage undergo greater dehydration in hypertonic medium but slower rehydration after returning to an isotonic medium than those at blastocysts stage. These characteristic can favor the expanded blastocysts during cryopreservation, making them less sensitive to an osmotic shock after thawing than embryos at blastocyst stage. Such slower rehydration may occur because embryos in expanded blastocyst stage have lower area/volume ratio than those in blastocyst stage. Embryos at late stage of development have more cells and greater blastocoel, resulting in a higher volume, which may take longer for initial recovery following dehydration.