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围产期母体营养不足会对后代下丘脑-垂体-肾上腺(HPA)轴进行编程。

Perinatal maternal undernutrition programs the offspring hypothalamo-pituitary-adrenal (HPA) axis.

作者信息

Lesage Jean, Sebaai Naima, Leonhardt Marion, Dutriez-Casteloot Isabelle, Breton Christophe, Deloof Sylvie, Vieau Didier

机构信息

Perinatal Stress Unit, Department of Adaptative Neurosciences and Physiology, University of Lille1, 59655, Villeneuve d'Ascq Cedex, France.

出版信息

Stress. 2006 Dec;9(4):183-98. doi: 10.1080/10253890601056192.

Abstract

There is now compelling evidence, coming both from animal and human studies that an early exposure to undernutrition is frequently associated with low birth weight and programs HPA axis alterations throughout the lifespan. Although animal models have reported conflicting findings arising from differences in experimental paradigms and species, they have clearly demonstrated that such programming not only affects the brain but also the pituitary corticotrophs and the adrenal cortex. In fetuses, maternal undernutrition reduces HPA axis function and implicates a reduction of placental 11beta-HSD2 activity and a greater transplacental transfer of glucocorticoids (GRs). In young adults, usually only fine HPA axis alterations were observed, whereas in older ones, maternal undernutrition was frequently associated with chronic hyperactivity of this neuroendocrine axis. In humans, evidence of HPA axis dysregulation in people who were small at birth has recently emerged. Thus, we suggest that such alterations in adults may be implicated in the aetiology of several disorders related to the metabolic syndrome as well as to immune or inflammatory diseases. To reverse such programming, recent experimental reports have shown that postnatal environmental interventions, dietary modifications and the use of agents modulating the epigenomic state could partly restore physiological functions and thus open new therapeutic strategies.

摘要

目前,来自动物和人体研究的有力证据表明,早期暴露于营养不良环境通常与低出生体重相关,并会在整个生命周期中导致下丘脑-垂体-肾上腺(HPA)轴功能改变。尽管动物模型因实验范式和物种差异而报告了相互矛盾的结果,但它们清楚地表明,这种程序化不仅会影响大脑,还会影响垂体促肾上腺皮质激素细胞和肾上腺皮质。在胎儿中,母体营养不良会降低HPA轴功能,并意味着胎盘11β-羟类固醇脱氢酶2(11β-HSD2)活性降低以及糖皮质激素(GRs)经胎盘转运增加。在年轻成年人中,通常仅观察到HPA轴的细微改变,而在老年人中,母体营养不良常常与该神经内分泌轴的慢性功能亢进有关。在人类中,最近出现了出生时体重较轻者HPA轴失调的证据。因此,我们认为成年人中的这种改变可能与几种与代谢综合征以及免疫或炎症性疾病相关的疾病的病因有关。为了逆转这种程序化,最近的实验报告表明,产后环境干预、饮食调整以及使用调节表观基因组状态的药物可以部分恢复生理功能,从而开辟新的治疗策略。

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