间歇性禁食能增加瘦小鼠的脂肪氧化,促进代谢灵活性,但不能促进肥胖的 2 型糖尿病小鼠的代谢灵活性。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM American journal of physiology. Endocrinology and metabolism Pub Date : 2024-10-01 Epub Date: 2024-08-28 DOI:10.1152/ajpendo.00255.2024
Meghan O Conn, Daniel M Marko, Jonathan D Schertzer
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引用次数: 0

摘要

肥胖和 2 型糖尿病(T2D)与代谢不灵活有关,其特点是在底物储存和利用途径之间切换的能力受损。肥胖期间代谢缺乏灵活性的典型表现是,尽管储存的脂质供应充足,但脂肪酸代谢的参与度较低。间歇性禁食(IF)可以促进新陈代谢的灵活性。然而,目前还不清楚肥胖症和 T2D 如何在反复间歇性禁食后改变代谢灵活性。雄性肥胖 db/db 小鼠和对照组 db/+ 小鼠每周禁食两次,每次 24 小时,连续禁食 10 周。这种 5:2 IF 方案不会改变 db/db 或 db/+ 小鼠的体重、身体成分、食物摄入量或体力活动。IF 后,db/db 小鼠在进食状态下脂肪酸氧化率较低,碳水化合物氧化率较高,这表明代谢脂质的灵活性较差。中频饲喂后,对照组 db/+ 小鼠在进食状态下脂肪酸氧化率较高,碳水化合物氧化率较低,这是代谢灵活性和脂质代谢参与度增加的特征。在空腹状态下,中频炉降低了对照组 db/+ 小鼠的碳水化合物氧化率,增加了脂肪酸氧化率,但肥胖 db/db 小鼠的脂肪酸氧化率却没有增加。中频饲喂后,db/db小鼠血清中的β-羟丁酸也低于对照组db/+小鼠。10周的中频炉可减少对照组db/+小鼠内脏脂肪组织中脂肪细胞的大小,但这种中频炉方案不会改变肥胖db/db小鼠脂肪细胞的大小。因此,中频炉可增加瘦小鼠的脂肪酸氧化和代谢灵活性,但在肥胖和 2 型糖尿病小鼠模型中却不存在这种适应性。
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Intermittent fasting increases fat oxidation and promotes metabolic flexibility in lean mice but not obese type 2 diabetic mice.

Obesity and type 2 diabetes (T2D) are associated with metabolic inflexibility, characterized by an impaired ability to switch between substrate storage and utilization pathways. Metabolic inflexibility during obesity is typified by lower engagement of fatty acid metabolism despite an ample supply of stored lipids. Intermittent fasting (IF) can promote metabolic flexibility. However, it is not clear how obesity and T2D alter metabolic flexibility after repeated IF. Male obese db/db and control db/+ mice were fasted for 24 h twice a week for 10 wk. This 5:2 IF regimen did not alter body mass, body composition, food intake, or physical activity in db/db or db/+ mice. After IF, db/db mice had lower fatty acid oxidation and higher carbohydrate oxidation in the fed state, indicating metabolic inflexibility to metabolize lipids. After IF, control db/+ mice had higher fatty acid oxidation and lower carbohydrate oxidation in the fed state, characteristic of metabolic flexibility, and increased engagement of lipid metabolism. In the fasted state, IF lowered carbohydrate oxidation and increased fatty acid oxidation in control db/+ mice but not in obese db/db mice. After IF, db/db mice also had lower serum β-hydroxybutyrate than control db/+ mice. Ten weeks of IF decreased adipocyte size in visceral adipose tissue of control db/+ mice, but this IF regimen did not change adipocyte size in obese db/db mice. Therefore, IF increases fatty acid oxidation and metabolic flexibility in lean mice, but this adaptation is absent in a mouse model of obesity and type 2 diabetes.NEW & NOTEWORTHY We show that a 5:2 intermittent fasting regimen can increase lipid oxidation without altering body mass in lean mice. Therefore, repeated intermittent fasting can increase metabolic flexibility without the need for (or prior to) weight loss. Intermittent fasting did not increase lipid oxidation in mice with obesity and type 2 diabetes, highlighting that obesity and/or type 2 diabetes limit changes in metabolic flexibility and mitigate increased fatty acid oxidation without weight loss during intermittent fasting.

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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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