Brownlow Milene L, Jung Seung H, Moore Raquel J, Bechmann Naomi, Jankord Ryan
Applied Neuroscience Branch, Warfighter Interface Division, Air Force Research Laboratory, Wright-Patterson Air Force BaseDayton, OH, USA.
Research Associateship Program, National Research Council, National Academies of ScienceWashington DC, USA.
Front Mol Neurosci. 2017 May 15;10:129. doi: 10.3389/fnmol.2017.00129. eCollection 2017.
Nutritional ketosis may enhance cerebral energy metabolism and has received increased interest as a way to improve or preserve performance and resilience. Most studies to date have focused on metabolic or neurological disorders while anecdotal evidence suggests that ketosis may enhance performance in the absence of underlying dysfunction. Moreover, decreased availability of glucose in the brain following stressful events is associated with impaired cognition, suggesting the need for more efficient energy sources. We tested the hypotheses that ketosis induced by endogenous or exogenous ketones could: (a) augment cognitive outcomes in healthy subjects; and (b) prevent stress-induced detriments in cognitive parameters. Adult, male, Sprague Dawley rats were used to investigate metabolic and behavioral outcomes in 3 dietary conditions: ketogenic (KD), ketone supplemented (KS), or NIH-31 control diet in both control or chronic stress conditions. Acute administration of exogenous ketones resulted in reduction in blood glucose and sustained ketosis. Chronic experiments showed that in control conditions, only KD resulted in pronounced metabolic alterations and improved performance in the novel object recognition test. The hypothalamic-pituitary-adrenal (HPA) axis response revealed that KD-fed rats maintained peripheral ketosis despite increases in glucose whereas no diet effects were observed in ACTH or CORT levels. Both KD and KS-fed rats decreased escape latencies on the third day of water maze, whereas only KD prevented stress-induced deficits on the last testing day and improved probe test performance. Stress-induced decrease in hippocampal levels of β-hydroxybutyrate was attenuated in KD group while both KD and KS prevented stress effects on BDNF levels. Mitochondrial enzymes associated with ketogenesis were increased in both KD and KS hippocampal samples and both endothelial and neuronal glucose transporters were affected by stress but only in the control diet group. Our results highlight the complex relationship between peripheral metabolism, behavioral performance and biochemical changes in the hippocampus. Endogenous ketosis improved behavioral and metabolic parameters associated with energy metabolism and cognition while ketone supplementation replicated the biochemical effects within the hippocampus but only showed modest effects on behavioral improvements.
营养性酮症可能会增强大脑能量代谢,作为一种改善或保持机能及恢复力的方法,它已引起了越来越多的关注。迄今为止,大多数研究都集中在代谢或神经紊乱方面,而轶事证据表明,在没有潜在功能障碍的情况下,酮症可能会提高机能。此外,应激事件后大脑中葡萄糖供应减少与认知受损有关,这表明需要更有效的能量来源。我们检验了以下假设:内源性或外源性酮诱导的酮症可以:(a)增强健康受试者的认知结果;(b)预防应激引起的认知参数损害。成年雄性Sprague Dawley大鼠用于研究三种饮食条件下的代谢和行为结果:生酮饮食(KD)、补充酮饮食(KS)或NIH-31对照饮食,分为对照或慢性应激条件。急性给予外源性酮导致血糖降低和持续的酮症。慢性实验表明,在对照条件下,只有KD导致明显而持久的代谢改变,并在新物体识别测试中提高了机能。下丘脑-垂体-肾上腺(HPA)轴反应显示,喂食KD的大鼠尽管血糖升高,但仍维持外周酮症,而促肾上腺皮质激素(ACTH)或皮质酮(CORT)水平未观察到饮食效应。喂食KD和KS的大鼠在水迷宫第三天的逃避潜伏期均缩短,而只有KD在最后测试日预防了应激引起的机能缺陷并改善了探针测试表现。KD组减轻了应激引起的海马中β-羟基丁酸水平的降低,而KD和KS均预防了应激对脑源性神经营养因子(BDNF)水平的影响。与酮生成相关的线粒体酶在KD和KS海马样本中均增加,内皮细胞和神经元葡萄糖转运体均受到应激的影响,但仅在对照饮食组中如此。我们的结果突出了外周代谢、行为表现和海马生化变化之间的复杂关系。内源性酮症改善了与能量代谢和认知相关的行为和代谢参数,而补充酮则在海马内复制了生化效应,但仅对行为改善显示出适度影响。