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饮食诱导肥胖的逆转增加了胰岛素向脑脊液中的转运,并恢复了雄性大鼠中枢胰岛素的厌食作用敏感性。

Reversal of diet-induced obesity increases insulin transport into cerebrospinal fluid and restores sensitivity to the anorexic action of central insulin in male rats.

机构信息

Departments of Psychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH 45237, USA.

出版信息

Endocrinology. 2013 Mar;154(3):1047-54. doi: 10.1210/en.2012-1929. Epub 2013 Jan 21.

DOI:10.1210/en.2012-1929
PMID:23337529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3578991/
Abstract

Diet-induced obesity (DIO) reduces the ability of centrally administered insulin to reduce feeding behavior and also reduces the transport of insulin from the periphery to the central nervous system (CNS). The current study was designed to determine whether reversal of high-fat DIO restores the anorexic efficacy of central insulin and whether this is accompanied by restoration of the compromised insulin transport. Adult male Long-Evans rats were initially maintained on either a low-fat chow diet (LFD) or a high-fat diet (HFD). After 22 weeks, half of the animals on the HFD were changed to the LFD, whereas the other half continued on the HFD for an additional 8 weeks, such that there were 3 groups: 1) a LFD control group (Con; n = 18), 2) a HFD-fed, DIO group (n = 17), and 3) a HFD to LFD, DIO-reversal group (DIO-rev; n = 18). The DIO reversal resulted in a significant reduction of body weight and epididymal fat weight relative to the DIO group. Acute central insulin administration (8 mU) reduced food intake and caused weight loss in Con and DIO-rev but not DIO rats. Fasting cerebrospinal fluid insulin was higher in DIO than Con animals. However, after a peripheral bolus injection of insulin, cerebrospinal fluid insulin increased in Con and DIO-rev rats but not in the DIO group. These data provide support for previous reports that DIO inhibits both the central effects of insulin and insulin's transport to the CNS. Importantly, DIO-rev restored sensitivity to the effects of central insulin on food intake and insulin transport into the CNS.

摘要

饮食诱导肥胖(DIO)降低了中枢给予胰岛素减少摄食行为的能力,也降低了胰岛素从外周向中枢神经系统(CNS)的转运。本研究旨在确定高脂肪 DIO 的逆转是否恢复了中枢胰岛素的厌食作用,以及这是否伴随着受损胰岛素转运的恢复。成年雄性 Long-Evans 大鼠最初维持在低脂饮食(LFD)或高脂肪饮食(HFD)。22 周后,HFD 组的一半动物改为 LFD,而另一半继续接受 HFD 喂养 8 周,因此有 3 组:1)LFD 对照组(Con;n = 18),2)HFD 喂养、DIO 组(n = 17)和 3)HFD 至 LFD、DIO 逆转组(DIO-rev;n = 18)。DIO 逆转导致体重和附睾脂肪重量相对于 DIO 组显著减少。急性中枢给予胰岛素(8 mU)可减少 Con 和 DIO-rev 大鼠的摄食量并导致体重减轻,但不能减少 DIO 大鼠的摄食量。DIO 大鼠的空腹脑脊液胰岛素高于 Con 组。然而,外周给予胰岛素后,Con 和 DIO-rev 大鼠的脑脊液胰岛素增加,但 DIO 组没有增加。这些数据支持先前的报告,即 DIO 抑制了胰岛素的中枢作用及其向 CNS 的转运。重要的是,DIO 逆转恢复了对中枢胰岛素对食物摄入和胰岛素向 CNS 转运的作用的敏感性。

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Inconsistencies in the assessment of food intake.饮食摄入评估的不一致性。
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