De Hertogh R, Vanderheyden I, Pampfer S, Robin D, Dufrasne E, Delcourt J
Physiology of Human Reproduction Research Unit, University of Louvain, School of Medicine, Brussels, Belgium.
Diabetes. 1991 May;40(5):641-7. doi: 10.2337/diab.40.5.641.
The effect of glucose and insulin on the in vitro development of the rat preimplantation embryo was studied by incubating rat blastocysts recovered on days 5 or 6 of pregnancy in the absence or presence of increasing levels of glucose and/or insulin for 24 or 48 h. A differential cell-staining method allowed the separate counting of inner cell mass (ICM) and trophectoderm (TE) cells at the end of the incubation period. In a high-glucose medium (17 mM), ICM and, to a lesser extent, TE developments were significantly and irreversibly inhibited. Low insulin concentrations (3 pM) stimulated ICM and TE development in the presence of 1.1 or 6 mM glucose. Higher insulin levels (30-600 pM) in a 6-mM glucose medium, resulted in a dose-dependent inhibition of ICM and, to a lesser extent, TE development after both 24 and 48 h. This insulin-induced inhibition was reversible if insulin was removed from the medium after 24 h. In the absence of glucose in the medium, insulin was neither stimulatory nor inhibitory on ICM growth. Dead-cell occurrence in ICM after a 48-h incubation increased with increasing glucose concentration in the medium. Insulin alone did not increase dead-cell number but enhanced the effect of glucose. These results show that, in the presence of glucose, insulin might be stimulatory (at low concentrations) or inhibitory (at higher concentrations) on ICM development. A high glucose level was also inhibitory and increased dead-cell occurrence. The data suggest that insulin and glucose might interact and modulate blastocyst development as a function of their respective concentrations.
通过将妊娠第5天或第6天回收的大鼠囊胚在不存在或存在浓度不断增加的葡萄糖和/或胰岛素的情况下培养24或48小时,研究了葡萄糖和胰岛素对大鼠植入前胚胎体外发育的影响。一种差异细胞染色方法使得在培养期结束时能够分别对内细胞团(ICM)和滋养外胚层(TE)细胞进行计数。在高葡萄糖培养基(17 mM)中,ICM以及程度较轻的TE发育受到显著且不可逆的抑制。低胰岛素浓度(3 pM)在存在1.1或6 mM葡萄糖的情况下刺激了ICM和TE的发育。在6 mM葡萄糖培养基中较高的胰岛素水平(30 - 600 pM),在24小时和48小时后均导致ICM发育呈剂量依赖性抑制,对TE发育的抑制程度较轻。如果在24小时后从培养基中去除胰岛素,这种胰岛素诱导的抑制是可逆的。在培养基中不存在葡萄糖的情况下,胰岛素对ICM生长既无刺激作用也无抑制作用。培养48小时后ICM中死细胞的出现随着培养基中葡萄糖浓度的增加而增加。单独的胰岛素不会增加死细胞数量,但会增强葡萄糖的作用。这些结果表明,在存在葡萄糖的情况下,胰岛素可能对ICM发育具有刺激作用(在低浓度时)或抑制作用(在高浓度时)。高葡萄糖水平也具有抑制作用并增加死细胞的出现。数据表明胰岛素和葡萄糖可能会相互作用,并根据它们各自的浓度调节囊胚发育。