Fukui Y, Lee E S, Araki N
Laboratory of Animal Genetics and Reproduction, Obihiro University of Agriculture and Veterinary Medicine, Japan.
J Anim Sci. 1996 Nov;74(11):2752-8. doi: 10.2527/1996.74112752x.
Three experiments investigated the effects of culture systems and renewal of medium (synthetic oviduct fluid medium (SOFM) supplemented with glutamine and amino acids) during in vitro development of in vitro-produced 2- to 4-cell bovine embryos. In Exp. 1, the early cleaved embryos were cultured under three different conditions for 186 h using 24-well dishes. The proportions of blastocysts (P < .05) and hatched blastocysts (P < .001) were lower for culture in SOFM + .8% BSA with renewal of medium at 48-h intervals (26.7 and 7.9%) than for cultures in SOFM + 10% human serum without renewal of medium (32.6 and 20.6%) and in SOFM + BSA without renewal of medium (32.2 and 23.0%). Two culture systems (well and microdrop) with or without renewal of medium (SOFM + BSA) were compared in Exp. 2 (186-h culture) and 3 (138-h culture). In Exp. 2, the microdrop system was superior (P < .05) to the well system for development of hatched blastocysts (19.1 and 11.7%), and the highest development to blastocysts (39.6%) and hatched blastocysts (27.8%) was observed in the microdrop system without renewal of medium. Experiment 3 also showed that the microdrop system was superior (P < .05) to the well system for development to blastocysts (32.7 and 27.2%), and the highest development rate to blastocysts (37.6%) occurred without renewal of medium. When the medium was not renewed in Exp. 2 and 3, the ammonium concentrations increased in both the well and microdrop systems. The results indicate that despite the reduction in ammonium concentrations resulting from medium renewal, renewal resulted in reduced development of embryos to hatched blastocysts in both the well and microdrop systems.
三项实验研究了培养系统以及在体外生产的2至4细胞牛胚胎体外发育过程中培养基(添加谷氨酰胺和氨基酸的合成输卵管液培养基(SOFM))更新的影响。在实验1中,使用24孔培养皿将早期分裂的胚胎在三种不同条件下培养186小时。与在不更换培养基的SOFM + 10%人血清(32.6%和20.6%)以及不更换培养基的SOFM + BSA(32.2%和23.0%)中培养相比,在每隔48小时更换培养基的SOFM + 0.8% BSA中培养的囊胚比例(P < 0.05)和孵化囊胚比例(P < 0.001)较低(分别为26.7%和7.9%)。在实验2(186小时培养)和实验3(138小时培养)中比较了两种培养系统(孔板和微滴)以及是否更换培养基(SOFM + BSA)的情况。在实验2中,微滴系统在孵化囊胚发育方面优于孔板系统(分别为19.1%和11.7%,P < 0.05),并且在不更换培养基的微滴系统中观察到最高的囊胚发育率(39.6%)和孵化囊胚发育率(27.8%)。实验3还表明,在囊胚发育方面微滴系统优于孔板系统(分别为32.7%和27.2%,P < 0.05),并且在不更换培养基时出现最高的囊胚发育率(37.6%)。在实验2和3中不更换培养基时,孔板和微滴系统中的铵浓度均升高。结果表明,尽管更换培养基会降低铵浓度,但更换培养基会导致孔板和微滴系统中胚胎发育至孵化囊胚的能力降低。