Cooper Michael A, McCoin Colin, Pei Dong, Thyfault John P, Koestler Devin, Wright Douglas E
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Exp Physiol. 2018 Sep;103(9):1206-1212. doi: 10.1113/EP087083. Epub 2018 Aug 8.
What is the central question of this study? Do peripheral sensory neurons metabolize fat-based fuel sources, and does a ketogenic diet modify these processes? What is the main finding and its importance We show that peripheral axons from mice fed a ketogenic diet respond to fat-based fuel sources with reduced respiration and H O emission compared with mice fed a control diet. These results add to our understanding of the responses of sensory neurons to neuropathy associated with poor diet, obesity and metabolic syndrome. These findings should be incorporated into current ideas of axonal protection and might identify how dietary interventions may change mitochondrial function in settings of sensory dysfunction.
Metabolic syndrome and obesity are increasing epidemics that significantly impact the peripheral nervous system and lead to negative changes in sensation and peripheral nerve function. Research to understand the consequences of diet, obesity and fuel usage in sensory neurons has commonly focused on glucose metabolism. Here, we tested whether mouse sensory neurons and nerves have the capacity to metabolize fat-based fuels (palmitoyl-CoA) and whether these effects are altered by feeding of a ketogenic (90% kcal fat) diet compared with a control diet (14% kcal fat). Male C57Bl/6 mice were placed on the diets for 10 weeks, and after the mice were killed, the dorsal root ganglion (DRG) and sciatic nerve (SN) were placed in an Oroboros oxygraph-2K to examine diet-induced alterations in metabolism (respiration) of palmitoyl-CoA and H O emission (fluorescence). In addition, RNAseq was performed on the DRG of mice fed a control or a ketogenic diet for 12 weeks, and genes associated with mitochondrial respiratory function were analysed. Our results suggest that the sciatic nerves from mice fed a ketogenic diet display reduced O respiration and H O emission when metabolizing palmitoyl-CoA compared with mice fed a control diet. Assessments of changes in mRNA gene expression reveal alterations in genes encoding the NADH dehydrogenase complex and complex IV, which could alter production of reactive oxygen species. These new findings highlight the ability of sensory neurons and axons to oxidize fat-based fuel sources and show that these mechanisms are adaptable to dietary changes.
本研究的核心问题是什么?外周感觉神经元是否代谢基于脂肪的燃料来源,生酮饮食是否会改变这些过程?主要发现及其重要性是什么?我们发现,与喂食对照饮食的小鼠相比,喂食生酮饮食的小鼠的外周轴突对基于脂肪的燃料来源的反应是呼吸作用和水排放减少。这些结果加深了我们对感觉神经元对与不良饮食、肥胖和代谢综合征相关的神经病变反应的理解。这些发现应纳入当前的轴突保护理念中,并可能确定饮食干预如何在感觉功能障碍的情况下改变线粒体功能。
代谢综合征和肥胖症正日益流行,对周围神经系统产生重大影响,并导致感觉和周围神经功能的负面变化。旨在了解饮食、肥胖和感觉神经元中燃料使用后果的研究通常集中在葡萄糖代谢上。在这里,我们测试了小鼠感觉神经元和神经是否有能力代谢基于脂肪的燃料(棕榈酰辅酶A),以及与对照饮食(14%千卡脂肪)相比,生酮(90%千卡脂肪)饮食的喂养是否会改变这些影响。将雄性C57Bl/6小鼠置于这些饮食中10周,在小鼠处死后,将背根神经节(DRG)和坐骨神经(SN)置于Oroboros oxygraph-2K中,以检查饮食诱导的棕榈酰辅酶A代谢(呼吸作用)和水排放(荧光)的变化情况。此外,对喂食对照饮食或生酮饮食12周的小鼠的DRG进行RNA测序,并分析与线粒体呼吸功能相关基因。我们的结果表明,与喂食对照饮食的小鼠相比,喂食生酮饮食的小鼠的坐骨神经在代谢棕榈酰辅酶A时显示出氧气呼吸作用和水排放减少。对mRNA基因表达变化的评估揭示了编码NADH脱氢酶复合体和复合体IV的基因的改变,这可能会改变活性氧的产生。这些新发现突出了感觉神经元和轴突氧化基于脂肪的燃料来源的能力,并表明这些机制可适应饮食变化。