Department of Neuroscience, University of Florida, Gainesville, FL 32611, USA.
University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Aging (Albany NY). 2020 May 5;12(9):7963-7984. doi: 10.18632/aging.103116.
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.
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。