首页> 外文期刊>Endocrinology >Maternal perinatal undernutrition drastically reduces postnatal leptin surge and affects the development of arcuate nucleus proopiomelanocortin neurons in neonatal male rat pups.
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Maternal perinatal undernutrition drastically reduces postnatal leptin surge and affects the development of arcuate nucleus proopiomelanocortin neurons in neonatal male rat pups.

机译:产妇围产期营养不良极大地减少了产后瘦素激增,并影响了新生雄性幼崽弓形核proopiomelanocortin神经元的发育。

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A growing body of evidence suggests that maternal undernutrition sensitizes the offspring to the development of energy balance metabolic disorders such as type 2 diabetes, dyslipidemia, and obesity. The present study aimed at examining the impact of maternal undernutrition on leptin plasma levels in newborn male rats and on the arcuate nucleus proopiomelanocortin (POMC) and neuropeptide Y (NPY) neurons that are major leptin targets. Using a model of perinatal maternal 50% food-restricted diet (FR50) in the rat, we evaluated leptin plasma levels and hypothalamic POMC and NPY gene expression from postnatal day (PND) 4 to PND30 in both control and FR50 offspring. In control rats, a postnatal peak of plasma leptin was observed between PND4 and PND14 that reached a maximal value at PND10 (5.17 +/- 0.53 ng/ml), whereas it was dramatically reduced in FR50 pups with the higher concentration at PND7 (0.93 +/- 0.23 ng/ml). In FR50 animals, using semiquantitative RT-PCR and in situ hybridization, we showed that the hypothalamic POMC mRNA level was decreased from PND14 until PND30, whereas NPY gene expression was not significantly modified. In PND21 FR50 animals, we observed strikingly reduced immunoreactive beta-endorphin nerve fibers projecting to the hypothalamic paraventricular nucleus without affecting NPY projections. Our data showed that maternal undernutrition drastically reduces the postnatal surge of plasma leptin, disturbing particularly the hypothalamic wiring as well as the gene expression of the anorexigenic POMC neurons in male rat pups. These alterations might contribute to the adult metabolic disorders resulting from perinatal growth retardation.
机译:越来越多的证据表明,母亲的营养不良使后代对能量平衡代谢紊乱(例如2型糖尿病,血脂异常和肥胖)的发展敏感。本研究旨在检查母体营养不良对新生雄性大鼠瘦素血浆水平的影响以及作为瘦素主要靶标的弓形核proopiomelanocortin(POMC)和神经肽Y(NPY)神经元的影响。使用大鼠围产期母亲50%食物限制饮食(FR50)模型,我们评估了对照和FR50后代从出生后第4天(PND)至PND30的瘦素血浆水平以及下丘脑POMC和NPY基因表达。在对照大鼠中,在PND4和PND14之间观察到血浆瘦素的产后高峰,在PND10(5.17 +/- 0.53 ng / ml)达到最大值,而在FR50幼仔中则显着降低,而在PND7(0.93 +/- 0.23 ng / ml)。在FR50动物中,使用半定量RT-PCR和原位杂交,我们显示从PND14到PND30,下丘脑POMC mRNA水平降低,而NPY基因表达没有明显改变。在PND21 FR50动物中,我们观察到显着减少的免疫反应性β-内啡肽神经纤维投射到下丘脑室旁核,而不会影响NPY投射。我们的数据表明,母亲营养不良会大大降低血浆瘦素的产后激增,特别是干扰下丘脑连线以及雄性幼崽中厌食性POMC神经元的基因表达。这些改变可能导致围生期发育迟缓导致的成人代谢紊乱。

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