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首页> 外文期刊>Endocrinology >Calorie-restricted weight loss reverses high-fat diet-induced ghrelin resistance, which contributes to rebound weight gain in a ghrelin-dependent manner
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Calorie-restricted weight loss reverses high-fat diet-induced ghrelin resistance, which contributes to rebound weight gain in a ghrelin-dependent manner

机译:热量限制的减肥可以逆转高脂饮食诱导的生长激素释放肽抵抗,从而以生长激素释放肽依赖性方式促进体重反弹

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Twelve weeks of high-fat diet feeding causes ghrelin resistance in arcuate neuropeptide Y (NPY)/agouti-related protein (AgRP) neurons. In the current study, we investigated whether diet-induced weight loss could restore NPY/AgRP neuronal responsiveness to ghrelin and whether ghrelin mediates rebound weight gain after calorie-restricted (CR) weight loss. Diet-induced obese (DIO) mice were allocated to one of two dietary interventions until they reached the weight of age-matched lean controls. DIO mice received chow diet ad libitum or chow diet with 40% CR. Chow-fed and high-fat-fed mice served as controls. Both dietary interventions normalized body weight, glucose tolerance, and plasma insulin. We show that diet-induced weight loss with CR increases total plasma ghrelin, restores ghrelin sensitivity, and increases hypothalamic NPY and AgRP mRNA expression. We propose that long-term DIO creates a higher body weight set-point and that weight loss induced by CR, as seen in the high-fat CR group, provokes the brain to protect the new higher set-point. This adaptation to weight loss likely contributes to rebound weight gain by increasing peripheral ghrelin concentrations and restoring the function of ghrelin-responsive neuronal populations in the hypothalamic arcuate nucleus. Indeed, we also show that DIO ghrelin-knockout mice exhibit reduced body weight regain after CR weight loss compared with ghrelin wild-type mice, suggesting ghrelin mediates rebound weight gain after CR weight loss.
机译:十二周的高脂饮食喂养会导致弓形神经肽Y(NPY)/ agouti相关蛋白(AgRP)神经元中的生长激素释放肽抵抗。在当前的研究中,我们调查了饮食引起的体重减轻是否可以恢复对ghrelin的NPY / AgRP神经元反应,以及ghrelin是否在卡路里限制(CR)减肥后介导反弹性体重增加。饮食诱发的肥胖(DIO)小鼠被分配到两种饮食干预中的一种,直到它们达到与年龄匹配的瘦对照组的体重。 DIO小鼠随意饮食或40%CR的饮食。饲喂高脂饲料的小鼠作为对照。两种饮食干预均可使体重,葡萄糖耐量和血浆胰岛素正常化。我们表明,饮食导致的体重减轻与CR增加总血浆生长素释放肽,恢复生长素释放肽的敏感性,并增加下丘脑NPY和AgRP mRNA表达。我们建议长期DIO会产生较高的体重设定点,而高脂CR组所见,CR引起的体重减轻会激发大脑保护新的较高设定点。对体重减轻的这种适应可能通过增加外周生长激素释放肽浓度并恢复下丘脑弓状核中生长激素释放肽反应性神经元种群的功能来促进体重增加。实际上,我们还表明,与生长素释放肽野生型小鼠相比,DIO生长素释放肽敲除小鼠在CR体重减轻后体重恢复降低,表明生长素释放肽在CR体重减轻后介导反弹体重增加。

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