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瘦素刺激生长板中的芳香酶:限制追赶生长效率。

Leptin stimulates aromatase in the growth plate: limiting catch-up growth efficiency.

机构信息

Sackler Faculty of MedicineTel Aviv University, Tel Aviv, Israel.

Felsenstein Medical Research CenterPetach Tikva, Israel.

出版信息

J Endocrinol. 2018 Jun;237(3):229-242. doi: 10.1530/JOE-18-0028. Epub 2018 Apr 3.

DOI:10.1530/JOE-18-0028
PMID:29615477
Abstract

Catch-up growth (CUG) in childhood is defined as periods of growth acceleration, after the resolution of growth attenuation causes, bringing the children back to their original growth trajectory. Sometimes, however, CUG is incomplete, leading to permanent growth deficit and short stature. The aim of this study was to investigate the mechanisms that limit nutritional-CUG. Specifically, we focused on the crosstalk between leptin, increased by re-feeding, and sex hormones, which increase with age. studies were performed in young male Sprague Dawley rats fed or subjected to 10/36 days of 40% food restriction followed by 90-120 days of re-feeding. studies were performed on ATDC5 cells. Analyses of mRNA and protein levels were done using qPCR and Western blot, respectively. CUG was complete in body weight and humerus length in animals that were food-restricted for 10 days but not for those food-restricted for 36 days. studies showed that leptin significantly increased aromatase gene expression and protein level as well as the expression of estrogen and leptin receptors in a dose- and time-dependent manner. The effect of leptin on aromatase was direct and was mediated through the MAPK/Erk, STAT3 and PI3K pathways. The crosstalk between leptin and aromatase in the growth plate suggests that re-feeding during puberty may lead to increased estrogen level and activity, and consequently, irreversible premature epiphyseal growth plate closure. These results may have important implications for the development of novel treatment strategies for short stature in children.

摘要

追赶性生长(CUG)是指生长衰减得到解决后,儿童出现生长加速的时期,使儿童回到其原始生长轨迹。然而,有时 CUG 是不完全的,导致永久性生长缺陷和身材矮小。本研究旨在探讨限制营养性 CUG 的机制。具体而言,我们专注于瘦素与年龄相关的性激素之间的相互作用,瘦素通过再喂养增加,而性激素随着年龄增长而增加。本研究在接受或经历 40%食物限制 10/36 天然后再喂养 90-120 天的年轻雄性 Sprague Dawley 大鼠中进行。在 ATDC5 细胞中进行了研究。使用 qPCR 和 Western blot 分别分析了 mRNA 和蛋白质水平。在动物中,10 天的食物限制完全恢复了体重和肱骨长度的 CUG,但 36 天的食物限制则不完全。研究表明,瘦素以剂量和时间依赖的方式显著增加了芳香酶基因表达和蛋白水平,以及雌激素和瘦素受体的表达。瘦素对芳香酶的作用是直接的,是通过 MAPK/Erk、STAT3 和 PI3K 途径介导的。瘦素与生长板中芳香酶的相互作用表明,青春期再喂养可能导致雌激素水平和活性增加,从而导致不可逆转的过早骺板生长板闭合。这些结果对于制定儿童身材矮小的新治疗策略可能具有重要意义。

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J Endocrinol. 2018 Jun;237(3):229-242. doi: 10.1530/JOE-18-0028. Epub 2018 Apr 3.
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