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脂肪组织是母体营养不足导致成人肥胖发育编程的关键靶点吗?

Is the adipose tissue a key target of developmental programming of adult adiposity by maternal undernutrition?

作者信息

Lukaszewski Marie-Amélie, Delahaye Fabien, Vieau Didier, Breton Christophe

机构信息

Unité Environnement Périnatal et Croissance; UPRES EA 4489; Université Lille-Nord de France; Equipe Dénutritions Maternelles Périnatales; Villeneuve d'Ascq, France.

出版信息

Adipocyte. 2012 Jan 1;1(1):64-67. doi: 10.4161/adip.18952.

Abstract

Epidemiological studies have shown that maternal undernutrition during pregnancy (MU) leads to intrauterine growth retardation and low birth weight, and may predispose individuals to the development of metabolic syndrome symptoms later in life such as overweight. Some clues from a model of prenatal maternal 70% food-restricted diet throughout gestation in pregnant female rats (FR30) suggest that the white adipose tissue (WAT) is a key target of MU fetal programming. Under standard diet, although showing a lean phenotype, adult FR30 male rats were predisposed to adiposity exhibiting higher serum leptin and corticosterone concentration, two hormones actively involved in WAT regulation. Although FR30 procedure does not worsen the metabolic syndrome features induced by HF diet, FR30HF rats gained more weight and showed hyperleptinemia suggesting increased adiposity. WAT FR30 adult rats revealed marked changes in transcript levels of several genes. In particular, leptin and Ob-Rb, many peptide precursors and receptors, factors involved in lipogenesis and glucocorticoid sensitivity mRNA expression levels as well as mechanisms involved in leptin sensitivity, were modified in FR30 offspring in depot-specific and diet-specific manners. These modifications might predispose for altered fat accumulation in adult male rat offspring.

摘要

流行病学研究表明,孕期母亲营养不足(MU)会导致胎儿宫内生长受限和低出生体重,并可能使个体在日后生活中易患代谢综合征症状,如超重。对怀孕雌性大鼠在整个妊娠期进行70%食物限制饮食的模型(FR30)的一些线索表明,白色脂肪组织(WAT)是MU胎儿编程的关键靶点。在标准饮食下,成年FR30雄性大鼠虽然表现出瘦型表型,但易患肥胖症,表现为血清瘦素和皮质酮浓度升高,这两种激素积极参与WAT调节。虽然FR30程序不会加重高脂饮食诱导的代谢综合征特征,但FR30HF大鼠体重增加更多,表现出高瘦素血症,提示肥胖增加。WAT FR30成年大鼠在几个基因的转录水平上显示出明显变化。特别是,瘦素和Ob-Rb、许多肽前体和受体、参与脂肪生成和糖皮质激素敏感性的因子的mRNA表达水平以及瘦素敏感性相关机制,在FR30后代中以特定储存部位和特定饮食的方式发生了改变。这些改变可能使成年雄性大鼠后代的脂肪积累发生改变。

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