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早期生活应激经历可能会减弱下丘脑瘦素信号传导。

Early life stress experience may blunt hypothalamic leptin signalling.

作者信息

Lee J H, Yoo S B, Kim J Y, Lee J Y, Kim B T, Park K, Jahng J W

机构信息

Department of Oral and Maxillofacial Surgery, Seoul National University School of Dentistry, Seoul, 110-768, Korea.

出版信息

J Biosci. 2017 Mar;42(1):131-138. doi: 10.1007/s12038-016-9656-3.

Abstract

The aim of this study was to investigate whether neonatal maternal separation (MS) - chronic stress experience in early life - affects the anorectic efficacy of leptin in the offspring at adolescence. Sprague-Dawley pups were separated from the dam daily for 3 h during postnatal day 1-14 or left undisturbed as non-handled controls (NH). NH and MS male pups received an intraperitoneal leptin (100 μg/kg) or saline on postnatal day (PND) 28, and then food intake and body weight gain were recorded. The hypothalamic levels of leptin-signalling-related genes, phosphorylated signal transducer and activator of transcription-3 (pSTAT3) and protein-tyrosine phosphatase 1B (PTP1B) were examined at 40 min after a single injection of leptin on PND 39 by immunohistochemistry and Western blot analysis. Leptin-induced suppressions in food intake and weight gain was observed in NH pups, but not in MS. Leptin increased pSTAT3 in the hypothalamic arcuate nucleus of NH pups, but not of MS. Interestingly, basal levels of the hypothalamic PTP1B and pSTAT3 were increased in MS pups compared with NH controls. The results suggest that neonatal MS experience may blunt the anorectic efficacy of leptin later in life, possibly in relation with increased expressions of PTP1B and/or pSTAT3 in the hypothalamus.

摘要

本研究的目的是调查新生儿母婴分离(MS)——早期生活中的慢性应激经历——是否会影响青春期后代中瘦素的食欲抑制功效。在出生后第1至14天,将斯普拉格-道利幼崽每天与母鼠分离3小时,或将其作为未受处理的对照(NH)不做干扰。在出生后第28天(PND),给NH和MS雄性幼崽腹腔注射瘦素(100μg/kg)或生理盐水,然后记录食物摄入量和体重增加情况。在PND 39单次注射瘦素40分钟后,通过免疫组织化学和蛋白质印迹分析检测下丘脑瘦素信号相关基因、磷酸化信号转导和转录激活因子3(pSTAT3)以及蛋白酪氨酸磷酸酶1B(PTP1B)的水平。在NH幼崽中观察到瘦素诱导的食物摄入量和体重增加的抑制,但在MS幼崽中未观察到。瘦素增加了NH幼崽下丘脑弓状核中的pSTAT3,但未增加MS幼崽中的pSTAT3。有趣的是,与NH对照相比,MS幼崽下丘脑PTP1B和pSTAT3的基础水平升高。结果表明,新生儿MS经历可能会削弱瘦素在生命后期的食欲抑制功效,这可能与下丘脑PTP1B和/或pSTAT3表达增加有关。

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