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Effects of Maternal Protein Malnutrition on Fetal Growth, Plasma Insulin-like Growth Factors, Insulin-like Growth Factor Binding Proteins, and Liver Insulin-like Growth Factor Gene Expression in the Rat

机译:母体蛋白营养不良对大鼠胎儿生长,血浆胰岛素样生长因子,胰岛素样生长因子结合蛋白和肝胰岛素样生长因子基因表达的影响

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We examined the effects of maternal dietary protein restriction on fetal growth and expression of IGF-I and -II, and IGF-binding proteins (IGFBP). We sought to dissociate the respective effects of maternal protein versus calorie restriction on growth indices and IGF synthesis by the neonates of protein-restricted dams. Pregnant Wistar rats (six to eight per group) fed a low (5%) protein diet throughout gestation had impaired body weight gain compared with controls fed a normal (20%) protein diet (by 45%, p p versus controls), although IGFBP-1, -2, and -4 were not significantly affected by the dietary protein intake. In pups of protein-restricted dams, the mean body and liver weight at birth was 15–20% less than that observed in the progeny from normal protein-fed dams (p p < 0.01). In contrast, neonatal plasma IGF-II and liver IGF-II mRNA concentrations were not significantly affected by the maternal protein malnutrition. Also, the plasma levels of IGFBP were not altered in the growth-retarded pups. Maternal protein restriction did not affect fetal and placental growth, plasma and liver IGF-I levels, and liver IGF-I mRNA abundance in 20-d-old fetuses. We conclude that intrauterine growth retardation caused by maternal protein malnutrition is associated with reduced neonatal expression of the IGF-I gene without obvious changes in IGF-II gene expression and plasma IGFBP concentrations. These results support the emerging evidence that IGF-I may play a role in the regulation of fetal growth and development.
机译:我们检查了母体饮食蛋白质限制对胎儿生长以及IGF-I和-II以及IGF结合蛋白(IGFBP)表达的影响。我们试图通过蛋白质限制性大坝的新生儿分离母体蛋白质与卡路里限制对生长指数和IGF合成的各自影响。与饲喂正常(20%)蛋白质饮食的对照组相比,怀孕的Wistar大鼠(每组六到八只)在整个妊娠过程中饲喂低(5%)蛋白质饮食的体重增加受到损害(与对照组相比,降低了45%) ,尽管IGFBP-1,-2和-4不受饮食蛋白质摄入量的显着影响。在受蛋白质限制的大坝幼崽中,出生时的平均体重和肝脏重量比正常的由蛋白质喂养的大坝后代低15-20%(p p <0.01)。相反,新生儿血浆IGF-II和肝脏IGF-II mRNA的浓度不受母体蛋白质营养不良的影响。同样,在生长迟缓的幼犬中,IGFBP的血浆水平没有改变。母体蛋白质限制不影响20天大胎儿的胎儿和胎盘生长,血浆和肝脏IGF-I水平以及肝脏IGF-I mRNA丰度。我们得出的结论是,由母体蛋白营养不良引起的宫内发育迟缓与IGF-I基因的新生儿表达降低有关,而IGF-II基因表达和血浆IGFBP浓度没有明显变化。这些结果支持了新出现的证据,即IGF-I可能在胎儿生长发育的调节中起作用。

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