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Comparison of two models of intrauterine growth restriction for early catch-up growth and later development of glucose intolerance and obesity in rats
39
Citations
28
References
2009
Year
NutritionMetabolic DisorderIntrauterine Growth RestrictionDex InjectionsCaloric RestrictionMaternal Food RestrictionObesityMetabolic SyndromeBody CompositionFetal Developmental ProgrammingMaternal NutritionPublic HealthAnimal PhysiologyGrowth HormoneGestational DiabetesMaternal HealthEndocrinologyDevelopmental BiologyPhysiologyDiabetesPediatricsGlucose IntoleranceMedicineEarly Catch-up Growth
Two models of intrauterine growth restriction, maternal food restriction (FR), and dexamethasone (DEX) exposure were compared for early postnatal catch-up growth and later development of glucose intolerance and obesity in Sprague-Dawley rats. Mated dams were randomly divided into three groups at 10 days gestational age. Group FR was food restricted (50% of nongestating rats) during the last 11 days of gestation; Group DEX received DEX injections during the last week of gestation, and Group CON, the control group, had no intervention. Birth weight, catch-up growth, body weight, and food intake were measured in male offspring for 22 wk. Body composition, blood glucose, and plasma insulin in response to a glucose load were assessed at 8, 16, and 22 wk. Pups from both FR and DEX dams had similarly lower birth weights than CON (22% and 25%, P < 0.0001), but catch-up growth, which occurred during the suckling period, was much more rapid in FR than DEX offspring (6 vs. 25 days, 95% CI). Postweaning, there were no significant differences between groups in food intake, body weight, body fat, and plasma insulin, but baseline plasma glucose at 22 wk and 2-h glucose area-under-the-curve at 8 and 22 wk were greater only in FR vs. CON offspring (P < 0.05), thereby contrasting with the lack of significant differences between DEX and CON. These results suggest that prenatal food restriction is a more sensitive model than DEX exposure for studies aimed at investigating the link between low birth weight, early postnatal catch-up growth, and later development of glucose intolerance.
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