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皮下和脑室内注射地塞米松激发试验显示,产前营养不良会降低大鼠下丘脑-垂体-肾上腺轴的敏感性。

Prenatal undernutrition decreases the sensitivity of the hypothalamo-pituitary-adrenal axis in rat, as revealed by subcutaneous and intra-paraventricular dexamethasone challenges.

作者信息

Navarrete Mario, Núñez Héctor, Ruiz Samuel, Soto-Moyano Rubén, Valladares Luis, White Allan, Pérez Hernán

机构信息

Laboratory of Hormones and Receptors, Institute of Nutrition and Food Technology (INTA), University of Chile, Santiago, Chile.

出版信息

Neurosci Lett. 2007 May 29;419(2):99-103. doi: 10.1016/j.neulet.2007.04.019. Epub 2007 Apr 13.

DOI:10.1016/j.neulet.2007.04.019
PMID:17481809
Abstract

Prenatal undernutrition is known to disturb the hypothalamo-pituitary-adrenal (HPA) axis, possibly through the programming of decreased expression of hypothalamic and pituitary glucocorticoid receptors. To test this hypothesis, we examined the corticosterone response to moderate subcutaneous (100 microg/kg) and intra-paraventricular (50 pmol, bilaterally) dexamethasone (DEX) challenges in normal eutrophic and prenatally undernourished young rats. Undernutrition was induced during fetal life by restricting the diet of pregnant mothers to 10 g daily, while mothers of eutrophic rats received the same diet ad libitum. At day 40 of postnatal life (i) undernourished rats showed increased plasma corticosterone concentration compared to normals; and (ii) subcutaneous and intra-paraventricular administrations of DEX led to reduced corticosterone levels in normal and undernourished animals, the effect of DEX (administered either peripherally or centrally) being significantly lower in the latter group. Results suggest that the low sensitivity of the HPA axis to DEX as well as the increased plasma corticosterone observed in prenatally undernourished rats could be due to the already reported glucocorticoid receptor underexpression found in the hypothalamus and pituitary of in utero undernourished animals, but alternative explanations involving central noradrenergic adaptive changes could also be possible.

摘要

已知产前营养不良会干扰下丘脑 - 垂体 - 肾上腺(HPA)轴,可能是通过下调下丘脑和垂体糖皮质激素受体的表达来实现的。为了验证这一假设,我们检测了正常营养良好和产前营养不良的幼鼠对中度皮下注射(100微克/千克)和脑室内注射(双侧各50皮摩尔)地塞米松(DEX)刺激的皮质酮反应。在胎儿期,通过将怀孕母鼠的饮食限制为每日10克来诱导营养不良,而营养良好的母鼠则随意进食相同的饮食。在出生后第40天,(i)与正常幼鼠相比,营养不良的幼鼠血浆皮质酮浓度升高;(ii)皮下和脑室内注射DEX导致正常和营养不良动物的皮质酮水平降低,DEX(外周或中枢给药)在后一组中的作用明显较低。结果表明,产前营养不良的大鼠中HPA轴对DEX的低敏感性以及观察到的血浆皮质酮升高,可能是由于已报道的子宫内营养不良动物下丘脑和垂体中糖皮质激素受体表达不足,但涉及中枢去甲肾上腺素能适应性变化的其他解释也有可能。

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