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

机译:代谢转换受衰老影响并且由酮症促进与糖原无关

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摘要

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.
机译:通过在禁食期间通过脂肪氧化进行新陈代谢,在糖酵解和酮症之间切换的能力可提高存活率。碳水化合物的限制或压力也会引起代谢转换。在老年大鼠中,糖酵解的酮适应性被延迟,但是尚未发现介导这种与年龄有关的损伤的因素。我们在接受标准饮食或低碳水化合物生酮饮食(KD)限时进食(TRF)的年轻和成年大鼠中,测量了糖酵解与酮症之间的代谢转换以及糖原动力学。单独的TRF可以逆转老年动物胰岛素相关代谢缺陷的标志物并加速代谢转换。但是,KD + TRF在这些变量上提供了附加的好处。值得注意的是,酮适应能力与糖原水平无关,而肾上腺皮质激素给药后,KD喂养的大鼠血糖升高。这项研究提供了对酮适应机制的新见解,证明了饮食干预措施可用于治疗整个生命周期的代谢障碍。

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