Laboratory of Histology and Embryology, School of Medicine, University of Athens, Athens, Greece.
Cell Mol Neurobiol. 2010 May;30(4):521-30. doi: 10.1007/s10571-009-9476-1. Epub 2009 Nov 10.
The peripubertal period is critical for the final maturation of circuits controlling energy homeostasis and stress response. However, the consequence of juvenile fat consumption on adult physiology is not clear. This study analyzed the adult consequences of post-weaning fat feeding on limbic-hypothalamic-pituitary-adrenal (HPA) axis components and on metabolic regulators of female rats. Wistar rats were fed either a high fat (HF) diet or the normal chow from weaning to puberty or to 3 months of age. Additional groups crossed their diets at puberty onset. Plasma leptin, insulin, and corticosterone levels were determined by radioimmunoassay and their brain receptors by western blot analysis. Adult HF-fed animals though not overweight, had higher corticosterone and reduced glucocorticoid receptor levels in the hypothalamus and hippocampus, compared to the controls. The alterations in HPA axis emerged already at puberty onset. Leptin receptor levels in the hypothalamus were reduced only by continuous fat feeding from weaning to adulthood. The pre-pubertal period appeared more vulnerable to diet-induced alterations in adulthood than the post-pubertal one. Switching from fat diet to normal chow at puberty onset restored most of the diet-induced alterations in the HPA axis. The corticosteroid circuit rather than the leptin or insulin system appears as the principal target for the peripubertal fat diet-induced effects in adult female rats.
青春期是控制能量平衡和应激反应的回路最终成熟的关键时期。然而,青春期前脂肪摄入对成年生理的影响尚不清楚。本研究分析了断奶后脂肪喂养对雌性大鼠边缘下丘脑垂体肾上腺(HPA)轴成分和代谢调节剂的成年后果。Wistar 大鼠从断奶到青春期或 3 个月大时分别喂食高脂肪(HF)饮食或正常饲料。其他组在青春期开始时交叉饮食。通过放射免疫分析测定血浆瘦素、胰岛素和皮质酮水平,并通过 Western blot 分析测定其脑受体。与对照组相比,成年 HF 喂养的动物尽管体重不超重,但在下丘脑和海马中的皮质酮和糖皮质激素受体水平降低。HPA 轴的改变早在青春期开始时就出现了。只有从断奶到成年持续喂食高脂肪饮食,下丘脑的瘦素受体水平才会降低。青春期前时期似乎比青春期后时期更容易受到饮食引起的成年期改变的影响。在青春期开始时从高脂肪饮食转换为正常饮食可恢复 HPA 轴大部分由饮食引起的改变。皮质类固醇回路而不是瘦素或胰岛素系统似乎是成年雌性大鼠青春期前高脂肪饮食诱导作用的主要靶标。