Department of Nutrition, Faculty of Medicine, University of Chile, Santiago 8380000, Chile.
Laboratory of Nutrition and Metabolic Regulation, Institute of Nutrition and Food Technology (INTA), University of Chile, Santiago 8380453, Chile.
Nutrients. 2023 Aug 11;15(16):3531. doi: 10.3390/nu15163531.
Fetal programming provides explanatory mechanisms for the currently high prevalence of gestational obesity. The endocannabinoid system (ECS) participates in the regulation of energy balance, and with a high-fat diet (HFD), it is overactivated. The aim of this study was to determine the effects of a nutritional intervention during pregnancy and lactation on obese female progenitors, on metabolic alterations of the offspring and on the involvement of ECS. Female mice (C57/BL/6-F0), 45 days old, and their offspring (males) were separated according to type of diet before and during gestation and lactation: CON-F1: control diet; HFD-F1 group: HFD (fat: 60% Kcal); INT-F1 group: HFD until mating and control diet (fat: 10% Kcal) afterward. Glucose tolerance and insulin sensitivity (IS) were tested at 2 and 4 months. At 120 days, mice were sacrificed, plasma was extracted for the determination of hormones, and livers for gene expression and the protein level determination of ECS components. INT-F1 group presented a lower IS compared to CON-F1, and normal levels of adiponectin and corticosterone in relation to the HFD-F1 group. The intervention increased hepatic gene expression for fatty-acid amide hydrolase and monoacylglycerol lipase enzymes; however, these differences were not observed at the protein expression level. Our results suggest that this intervention model normalized some hormonal parameters and hepatic mRNA levels of ECS components that were altered in the offspring of progenitors with pre-pregnancy obesity.
胎儿编程为目前妊娠期肥胖症的高发提供了解释机制。内源性大麻素系统 (ECS) 参与能量平衡的调节,而高脂肪饮食 (HFD) 会使其过度激活。本研究旨在确定在妊娠和哺乳期进行营养干预对肥胖雌性前体的影响,对后代代谢改变的影响以及 ECS 的参与情况。将 45 天大的雌性小鼠 (C57/BL/6-F0) 及其后代 (雄性) 根据妊娠和哺乳期前的饮食类型进行分离:CON-F1:对照饮食;HFD-F1 组:HFD(脂肪:60%卡路里);INT-F1 组:HFD 直至交配,然后改为对照饮食(脂肪:10%卡路里)。在 2 个月和 4 个月时测试葡萄糖耐量和胰岛素敏感性 (IS)。在 120 天时,处死小鼠,提取血浆以测定激素,并提取肝脏以测定 ECS 成分的基因表达和蛋白水平。与 HFD-F1 组相比,INT-F1 组的 IS 较低,而脂联素和皮质酮水平正常。干预增加了脂肪酸酰胺水解酶和单酰基甘油脂肪酶基因在肝脏中的表达;然而,在蛋白表达水平上并未观察到这些差异。我们的结果表明,这种干预模型使前体妊娠前肥胖的后代中改变的一些激素参数和 ECS 成分的肝 mRNA 水平正常化。