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喂食致肥胖饮食的小鼠中,与体重增加相关的摄食行为和能量平衡随时间的变化。

Time dependent changes in feeding behavior and energy balance associated with weight gain in mice fed obesogenic diets.

作者信息

Fathi Payam A, Bales Michelle B, Ayala Julio E

出版信息

bioRxiv. 2024 Mar 5:2024.01.10.575043. doi: 10.1101/2024.01.10.575043.

Abstract

UNLABELLED

Obesity is characterized by dysregulated homeostatic mechanisms resulting in positive energy balance, yet when this dysregulation occurs is unknown. We assessed the time course of alterations to behaviors promoting weight gain in male and female mice switched to obesogenic 60% or 45% high fat diet (HFD). Switching mice to obesogenic diets promotes transient bouts of hyperphagia during the first 2 weeks followed by persistent caloric hyperphagia. Energy expenditure increases but not sufficiently to offset increased caloric intake, resulting in a sustained net positive energy balance. Hyperphagia is associated with consumption of calorically larger meals (impaired satiation) more frequently (impaired satiety) particularly during the light-cycle. Running wheel exercise delays weight gain in 60% HFD-fed male mice by enhancing satiation and increasing energy expenditure. However, exercise effects on satiation are no longer apparent after 2 weeks, coinciding with weight gain. Thus, exposure to obesogenic diets engages homeostatic regulatory mechanisms for ∼2 weeks that ultimately fail, and consequent weight gain is characterized by impaired satiation and satiety. Insights into the etiology of obesity can be obtained by investigating changes to satiation and satiety mechanisms during the initial ∼2 weeks of HFD exposure.

WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT?: Obesity is associated with dysregulated homeostatic mechanisms.Increased caloric consumption contributes to obesity.Obese rodents tend to eat larger, more frequent meals.

WHAT ARE THE NEW FINDINGS IN YOUR MANUSCRIPT?: Exposure to obesogenic diets promotes transient attempts to maintain weight homeostasis.After ∼2 weeks, caloric hyperphagia exceeds increased energy expenditure, promoting weight gain.This is associated with consumption of larger, more frequent meals.

HOW MIGHT YOUR RESULTS CHANGE THE DIRECTION OF RESEARCH OR THE FOCUS OF CLINICAL PRACTICE?: Our findings suggest that molecular studies focusing on mechanisms that regulate meal size and frequency, particularly those engaged during the first ∼2 weeks of obesogenic diet feeding that eventually fail, can provide unique insight into the etiology of obesity.

摘要

未标注

肥胖的特征是体内稳态机制失调,导致能量正平衡,但这种失调何时发生尚不清楚。我们评估了雄性和雌性小鼠切换到致肥胖的60%或45%高脂肪饮食(HFD)后,促进体重增加行为的变化时间进程。将小鼠切换到致肥胖饮食会在最初2周内促进短暂的食欲亢进发作,随后是持续的热量摄入过多。能量消耗增加,但不足以抵消热量摄入的增加,导致持续的净能量正平衡。食欲亢进与热量更高的餐食摄入(饱腹感受损)更频繁(饱腹感受损)有关,尤其是在光照周期。跑步锻炼通过增强饱腹感和增加能量消耗来延迟60%HFD喂养的雄性小鼠的体重增加。然而,2周后运动对饱腹感的影响不再明显,与体重增加同时出现。因此,接触致肥胖饮食会使体内稳态调节机制持续约2周,最终失效,随后的体重增加表现为饱腹感和饱腹感受损。通过研究HFD暴露最初约2周内饱腹感和饱腹感机制的变化,可以深入了解肥胖的病因。

关于该主题已知的信息

肥胖与体内稳态机制失调有关。热量消耗增加导致肥胖。肥胖的啮齿动物往往进食量更大、更频繁。

您的手稿中的新发现

接触致肥胖饮食会促进维持体重稳态的短暂尝试。约2周后,热量摄入过多超过能量消耗增加,促进体重增加。这与更大、更频繁的餐食摄入有关。

您的结果可能如何改变研究方向或临床实践重点

我们的研究结果表明,专注于调节餐食大小和频率机制的分子研究,特别是在致肥胖饮食喂养最初约2周内起作用但最终失效的那些机制,可以为肥胖的病因提供独特的见解。

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