Fraser R B, Waite S L, Wood K A, Martin K L
Academic Unit of Reproductive and Developmental Medicine, University of Sheffield, Level 4, Jessop Wing, Tree Root Walk, Sheffield S10 2SF, UK.
Hum Reprod. 2007 Dec;22(12):3059-68. doi: 10.1093/humrep/dem318. Epub 2007 Oct 12.
The aim of this study is to model the processes of early embryopathy seen in human pregnancy complicated by maternal hyperglycemia secondary to maternal diabetes using a mouse embryo culture system.
Female mice were superovulated and mated in pairs. Two-cell embryos were harvested from the oviducts and cultured in vitro in KSOM medium (synthetic oviductal medium enriched with potassium) supplemented with 0.2, 5.56, 15.56 or 25.56 mM d-glucose. Cell proliferation, differentiation and apoptosis were assessed. Experiments were performed in constant, embryos exposed to a particular concentration of glucose (0.2, 5.56, 15.56 or 25.56 mM) from harvest to either Day 5 post fertilization (pf) or Day 8 pf, and fluctuating, embryos exposed to alternate high 25.56 mM and normal 5.56 mM concentrations of glucose between harvest and Day 5 pf, glycemic culture.
Expected levels of blastocyst formation and hatching were seen at 0.2 and 5.56 mM concentrations of glucose but both were impaired at higher concentrations (chi(2), P < 0.005; P < 0.001). Total cell numbers (P < 0.002) and cell allocation to the inner cell mass (P < 0.01) were reduced, but with no evidence of enhanced apoptosis in the hyperglycemic cultures. Variation in hyperglycemic exposure of the embryos on Days 2, 3 and 4 showed no adverse effects of hyperglycemia up to 24 h, but 48 and 72 h exposures were equally embryopathic (P < 0.01).
Hyperglycemic exposure for >24 h is toxic to early embryo development. These findings may explain the lower than expected implantation rates and higher than expected rates of congenital abnormality and early pregnancy loss seen in patients with diabetes, particularly those with poor diabetic control.
本研究的目的是使用小鼠胚胎培养系统对人类妊娠中因母体糖尿病继发母体高血糖而出现的早期胚胎病变过程进行建模。
对雌性小鼠进行超排卵并成对交配。从输卵管中收集二细胞胚胎,并在添加了0.2、5.56、15.56或25.56 mM d-葡萄糖的KSOM培养基(富含钾的合成输卵管培养基)中进行体外培养。评估细胞增殖、分化和凋亡情况。实验分为恒定组,即胚胎从收获到受精后第5天(pf)或第8天pf暴露于特定浓度的葡萄糖(0.2、5.56、15.56或25.56 mM);以及波动组,即胚胎在收获到第5天pf期间暴露于交替的高浓度25.56 mM和正常浓度5.56 mM的葡萄糖,进行血糖培养。
在0.2和5.56 mM葡萄糖浓度下观察到了预期水平的囊胚形成和孵化,但在较高浓度下两者均受损(卡方检验,P < 0.005;P < 0.001)。总细胞数(P < 0.002)和分配到内细胞团的细胞数(P < 0.01)减少,但在高血糖培养中没有凋亡增加的证据。胚胎在第2、3和4天高血糖暴露的变化显示,长达24小时的高血糖没有不良影响,但48小时和72小时的暴露同样具有胚胎毒性(P < 0.01)。
高血糖暴露超过24小时对早期胚胎发育有毒性。这些发现可能解释了糖尿病患者中低于预期的着床率以及高于预期的先天性异常和早期妊娠丢失率,尤其是那些糖尿病控制不佳的患者。