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能量限制的配对喂养可使饮食诱导肥胖小鼠海马中低水平的脑源性神经营养因子/酪氨酸激酶B mRNA表达恢复正常,但腹内侧下丘脑核中的表达则不然。

Energy-restricted pair-feeding normalizes low levels of brain-derived neurotrophic factor/tyrosine kinase B mRNA expression in the hippocampus, but not ventromedial hypothalamic nucleus, in diet-induced obese mice.

作者信息

Yu Y, Wang Q, Huang X-F

机构信息

Centre for Translational Neuroscience, School of Health Sciences, University of Wollongong, Northfield Avenue, NSW 2522, Australia.

出版信息

Neuroscience. 2009 May 5;160(2):295-306. doi: 10.1016/j.neuroscience.2009.01.078. Epub 2009 Feb 13.

DOI:10.1016/j.neuroscience.2009.01.078
PMID:19217934
Abstract

Brain-derived neurotrophic factor (BDNF) and its receptor tyrosine kinase B (TrkB) are closely associated with the regulation of energy homeostasis, but their roles in diet-induced obesity have not been explored. Using dietary interventions, this study examined regional changes of BDNF and TrkB mRNA expression in different brain regions of diet-induced obese (DIO) and resistant (DR) mice in response to high-fat (HF), energy-restricted pair-feeding and low fat (LF) diets. Using in situ hybridization, DIO mice had significantly decreased levels of BDNF mRNA expression (-32% to -37%) and TrkB (-21% to -23%) in the hippocampus compared to DR mice on an HF diet, but not on energy-restricted pair-feeding and LF diets. In the ventromedial hypothalamic nucleus (VMH), BDNF expression was decreased in DIO mice on HF (-23%) and energy-restricted pair-feeding (-21%) diets. Furthermore, the VMH BDNF expression was negatively correlated with blood glucose but positively correlated with plasma adiponectin. These findings suggest that decreased hippocampal BDNF and TrkB expression plays an important role in high-fat diet induced obesity. A lower baseline BDNF mRNA expression in the VMH of DIO mice after normalization of body weight may indicate their intrinsic nature or an elevated body weight set point to drive body weight gain.

摘要

脑源性神经营养因子(BDNF)及其受体酪氨酸激酶B(TrkB)与能量稳态的调节密切相关,但其在饮食诱导肥胖中的作用尚未得到研究。本研究采用饮食干预方法,检测了饮食诱导肥胖(DIO)小鼠和抗肥胖(DR)小鼠不同脑区中BDNF和TrkB mRNA表达的区域变化,这些小鼠分别喂食高脂(HF)、能量限制配对喂养和低脂(LF)饮食。通过原位杂交技术发现,与喂食HF饮食的DR小鼠相比,DIO小鼠海马体中BDNF mRNA表达水平显著降低(-32%至-37%),TrkB表达水平也显著降低(-21%至-23%),但在能量限制配对喂养和LF饮食组中未出现这种情况。在腹内侧下丘脑核(VMH)中,喂食HF(-23%)和能量限制配对喂养(-21%)饮食的DIO小鼠中BDNF表达降低。此外,VMH中BDNF表达与血糖呈负相关,但与血浆脂联素呈正相关。这些发现表明,海马体中BDNF和TrkB表达降低在高脂饮食诱导的肥胖中起重要作用。体重正常化后,DIO小鼠VMH中较低的基线BDNF mRNA表达可能表明其内在特性或体重设定点升高,从而导致体重增加。

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