Oliver M H, Harding J E, Breier B H, Gluckman P D
Research Centre for Developmental Medicine and Biology, School of Medicine, University of Auckland, New Zealand.
Reprod Fertil Dev. 1996;8(1):167-72. doi: 10.1071/rd9960167.
We investigated the effect of restoration of normoglycaemia or normoinsulinaemia in fetuses of starved ewes on plasma IGF-I and IGF-II concentrations. Paired maternal and fetal blood samples were taken during an initial 2-day control period, after 48 h of maternal starvation, during 24 h fetal infusion of glucose (n = 6) or insulin (n = 4) while maintaining maternal starvation and after 48 h maternal refeeding. After 48 h starvation maternal and fetal plasma IGF-I, insulin and blood glucose fell (maternal IGF-I 38.9 +/- 3.6 to 16.4 +/- 1.8 nM and fetal IGF-I 13.2 +/- 0.8 to 7.1 +/- 0.7 nM, both P < 0.05). Fetal plasma IGF-II also fell (147.8 +/- 9.1 to 112.2 +/- 3.8 nM, P < 0.05), but maternal plasma IGF-II rose (71.8 +/- 6.3 to 88.8 +/- 9.2 nM, P = 0.10). Fetal glucose replacement raised fetal plasma IGF-I (11.4 +/- 1.2 nM), IGF-II (149.7 +/- 6.5 nM), insulin and blood glucose to near control values (all P < 0.05). Fetal insulin replacement raised fetal plasma IGF-I (9.0 +/- 0.6 nM) and insulin (all P < 0.05) while IGF-II (105.2 +/- 8.4 nM) and blood glucose remained depressed. Neither fetal infusion had any significant effect on maternal plasma IGF-I (13.1 +/- 1.6 nM), IGF-II (77.5 +/- 8.7 nM), insulin or blood glucose. After 48 h maternal refeeding fetal IGF-I (12.4 +/- 0.4 nM), fetal IGF-II (158.4 +/- 8.9 nM), maternal IGF-II (67.1 +/- 3.0 nM), maternal and fetal insulin and glucose had returned to near control values in both groups. Maternal IGF-I remained below control values (24.7 +/- 2.5 nM, P < 0.05). The data suggest that fetal IGF-I and IGF-II are independently regulated in the fetal circulation. While glucose plays an important role in the regulation of both IGF-I and IGF-II, the influence of glucose on fetal IGF-I is likely to be mediated by insulin, whereas for IGF-II the effect of glucose is insulin-independent.
我们研究了在饥饿母羊的胎儿中恢复正常血糖或正常胰岛素血症对血浆胰岛素样生长因子-I(IGF-I)和胰岛素样生长因子-II(IGF-II)浓度的影响。在初始2天的对照期、母羊饥饿48小时后、在维持母羊饥饿状态下胎儿输注葡萄糖24小时(n = 6)或胰岛素24小时(n = 4)期间以及母羊重新喂食48小时后,采集配对的母血和胎儿血样本。饥饿48小时后,母羊和胎儿的血浆IGF-I、胰岛素和血糖均下降(母羊IGF-I从38.9±3.6 nM降至16.4±1.8 nM,胎儿IGF-I从13.2±0.8 nM降至7.1±0.7 nM,两者P < 0.05)。胎儿血浆IGF-II也下降(从147.8±9.1 nM降至112.2±3.8 nM,P < 0.05),但母羊血浆IGF-II升高(从71.8±6.3 nM升至88.8±9.2 nM,P = 0.10)。胎儿葡萄糖替代使胎儿血浆IGF-I(11.4±1.2 nM)、IGF-II(149.7±6.5 nM)、胰岛素和血糖升高至接近对照值(均P < 0.05)。胎儿胰岛素替代使胎儿血浆IGF-I(9.0±0.6 nM)和胰岛素升高(均P < 0.05),而IGF-II(105.2±8.4 nM)和血糖仍处于较低水平。两种胎儿输注对母羊血浆IGF-I(13.1±1.6 nM)、IGF-II(77.5±8.7 nM)、胰岛素或血糖均无显著影响。母羊重新喂食48小时后,两组胎儿的IGF-I(12.4±0.4 nM)、胎儿IGF-II(158.4±8.9 nM)、母羊IGF-II(67.1±3.0 nM)、母羊和胎儿的胰岛素及血糖均恢复至接近对照值。母羊IGF-I仍低于对照值(24.7±2.5 nM,P < 0.