Laboratory of Endocrine Physiology, Department of Physiological Sciences, Biology Institute, State University of Rio de Janeiro, Brazil.
J Physiol. 2012 Nov 1;590(21):5503-18. doi: 10.1113/jphysiol.2012.240655. Epub 2012 Aug 6.
Maternal nutritional status affects the future development of offspring. Both undernutrition and overnutrition in critical periods of life (gestation or lactation) may cause several hormonal changes in the pups and programme obesity in the adult offspring. We have shown that hyperleptinaemia during lactation results in central leptin resistance, higher adrenal catecholamine secretion, hyperthyroidism, and higher blood pressure and heart rate in the adult rats. Here, we evaluated the effect of a maternal isocaloric high-fat diet on breast milk composition and its impact on leptinaemia, energy metabolism, and adrenal and thyroid function of the offspring at weaning. We hypothesised that the altered source of fat in the maternal diet even under normal calorie intake would disturb the metabolism of the offspring. Female Wistar rats were fed a normal (9% fat; C group) or high-fat diet (29% fat as lard; HF group) for 8 weeks before mating and during pregnancy and lactation. HF mothers presented increased total body fat content after 8 weeks (+27%, P < 0.05) and a similar fat content at the end of lactation. In consequence, the breast milk from the HF group had higher concentration of protein (+18%, P < 0.05), cholesterol (+52%, P < 0.05) and triglycerides (+86%, P < 0.05). At weaning, HF offspring had increased body weight (+53%, P < 0.05) and adiposity (2 fold, P < 0.05), which was associated with lower β3-adrenoreceptor content in adipose tissue (-40%, P < 0.05). The offspring also presented hyperglycaemia (+30%, P < 0.05) and hyperleptinaemia (+62%, P < 0.05). In the leptin signalling pathway in the hypothalamus, we found lower p-STAT3/STAT3 (-40%, P < 0.05) and SOCS3 (-55%, P < 0.05) content in the arcuate nucleus, suggesting leptin resistance. HF offspring also had higher adrenal catecholamine content (+17%, P < 0.05), liver glycogen content (+50%, P < 0.05) and hyperactivity of the thyroid axis at weaning. Our results suggest that a high fat diet increases maternal body fat and this additional energy is transferred to the offspring during lactation, since at weaning the dams had normal fat and the pups were obese. The higher fat and protein concentrations in the breast milk seemed to induce early overnutrition in the HF offspring. In addition to storing energy as fat, the HF offspring had a larger reserve of glycogen and hyperglycaemia that may have resulted from increased gluconeogenesis. Hyperleptinaemia may stimulate both adrenal medullary and thyroid function, which may contribute to the development of cardiovascular diseases. These early changes induced by the maternal high-fat diet may contribute to development of metabolic syndrome.
母体营养状况会影响后代的未来发育。生命关键期(妊娠或哺乳期)的营养不足和营养过剩都可能导致幼崽的几种激素变化,并导致成年后代肥胖。我们已经表明,哺乳期的高瘦素血症会导致中枢性瘦素抵抗、肾上腺儿茶酚胺分泌增加、甲状腺功能亢进、成年大鼠的血压和心率升高。在这里,我们评估了母体等热量高脂肪饮食对母乳成分的影响及其对断奶后代瘦素血症、能量代谢、肾上腺和甲状腺功能的影响。我们假设,即使在正常热量摄入的情况下,母体饮食中脂肪来源的改变也会扰乱后代的新陈代谢。雌性 Wistar 大鼠在交配前 8 周和妊娠及哺乳期期间分别喂食正常(9%脂肪;C 组)或高脂肪饮食(29%脂肪作为猪油;HF 组)。8 周后,HF 组的母体总体脂含量增加(增加 27%,P<0.05),哺乳期结束时的体脂含量相似。因此,HF 组的母乳中蛋白质浓度增加(增加 18%,P<0.05)、胆固醇(增加 52%,P<0.05)和甘油三酯(增加 86%,P<0.05)。断奶时,HF 后代体重增加(增加 53%,P<0.05)和肥胖(增加 2 倍,P<0.05),这与脂肪组织中β3-肾上腺素能受体含量降低(减少 40%,P<0.05)有关。后代还出现高血糖(增加 30%,P<0.05)和高瘦素血症(增加 62%,P<0.05)。在大脑下丘脑的瘦素信号通路中,我们发现弓状核中 p-STAT3/STAT3(减少 40%,P<0.05)和 SOCS3(减少 55%,P<0.05)的含量降低,表明瘦素抵抗。HF 后代的肾上腺儿茶酚胺含量也较高(增加 17%,P<0.05),肝糖原含量(增加 50%,P<0.05)和甲状腺轴的活性在断奶时也较高。我们的结果表明,高脂肪饮食会增加母体脂肪,这些额外的能量在哺乳期转移给后代,因为断奶时母体的脂肪正常,而幼崽肥胖。母乳中较高的脂肪和蛋白质浓度似乎导致 HF 后代早期营养过剩。除了将能量储存为脂肪外,HF 后代还具有更大的糖原储备和高血糖,这可能是由于糖异生增加所致。高瘦素血症可能会刺激肾上腺髓质和甲状腺功能,这可能导致心血管疾病的发展。母体高脂肪饮食引起的这些早期变化可能导致代谢综合征的发展。