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代谢转换受到衰老的影响,而酮症独立于糖原促进了代谢转换。

Metabolic switching is impaired by aging and facilitated by ketosis independent of glycogen.

机构信息

Department of Neuroscience, University of Florida, Gainesville, FL 32611, USA.

University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Aging (Albany NY). 2020 May 5;12(9):7963-7984. doi: 10.18632/aging.103116.

Abstract

The ability to switch between glycolysis and ketosis promotes survival by enabling metabolism through fat oxidation during periods of fasting. Carbohydrate restriction or stress can also elicit metabolic switching. Keto-adapting from glycolysis is delayed in aged rats, but factors mediating this age-related impairment have not been identified. We measured metabolic switching between glycolysis and ketosis, as well as glycogen dynamics, in young and aged rats undergoing time-restricted feeding (TRF) with a standard diet or a low carbohydrate ketogenic diet (KD). TRF alone reversed markers of insulin-related metabolic deficits and accelerated metabolic switching in aged animals. A KD+TRF, however, provided additive benefits on these variables. Remarkably, the ability to keto-adapt was not related to glycogen levels and KD-fed rats showed an enhanced elevation in glucose following epinephrine administration. This study provides new insights into the mechanisms of keto-adaptation demonstrating the utility of dietary interventions to treat metabolic impairments across the lifespan.

摘要

在禁食期间,通过脂肪氧化进行代谢的能力,使糖酵解和酮体生成之间的转换能力得以切换,从而促进了生存。碳水化合物限制或应激也可以引发代谢转换。在老年大鼠中,从糖酵解向酮体生成的适应被延迟,但介导这种与年龄相关的损伤的因素尚未确定。我们在接受限时喂养(TRF)的年轻和老年大鼠中测量了糖酵解和酮体生成之间的代谢转换,以及糖原动力学,TRF 本身就可以逆转与胰岛素相关的代谢缺陷的标志物,并加速老年动物的代谢转换。然而,KD+TRF 在这些变量上提供了额外的益处。值得注意的是,酮体生成的适应能力与糖原水平无关,并且 KD 喂养的大鼠在肾上腺素给药后表现出葡萄糖的显著升高。这项研究为酮体生成的适应机制提供了新的见解,证明了饮食干预在整个生命周期中治疗代谢损伤的效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b255/7244089/ac2a6e126682/aging-12-103116-g001.jpg

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