Suppr超能文献

食用生酮饮食的小鼠外周神经中线粒体活性氧生成减少。

Reduced mitochondrial reactive oxygen species production in peripheral nerves of mice fed a ketogenic diet.

作者信息

Cooper Michael A, McCoin Colin, Pei Dong, Thyfault John P, Koestler Devin, Wright Douglas E

机构信息

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.

出版信息

Exp Physiol. 2018 Sep;103(9):1206-1212. doi: 10.1113/EP087083. Epub 2018 Aug 8.

Abstract

NEW FINDINGS

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.

ABSTRACT

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.

摘要

新发现

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。

摘要

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。

相似文献

1
Reduced mitochondrial reactive oxygen species production in peripheral nerves of mice fed a ketogenic diet.
Exp Physiol. 2018 Sep;103(9):1206-1212. doi: 10.1113/EP087083. Epub 2018 Aug 8.
2
A ketogenic diet reduces metabolic syndrome-induced allodynia and promotes peripheral nerve growth in mice.
Exp Neurol. 2018 Aug;306:149-157. doi: 10.1016/j.expneurol.2018.05.011. Epub 2018 May 17.
4
High Dietary Fat Consumption Impairs Axonal Mitochondrial Function .
J Neurosci. 2021 May 12;41(19):4321-4334. doi: 10.1523/JNEUROSCI.1852-20.2021. Epub 2021 Mar 30.
5
Activation of NLRP3 inflammasome in peripheral nerve contributes to paclitaxel-induced neuropathic pain.
Mol Pain. 2017 Jan-Dec;13:1744806917719804. doi: 10.1177/1744806917719804.
8
Structural and Functional Rescue of Chronic Metabolically Stressed Optic Nerves through Respiration.
J Neurosci. 2018 May 30;38(22):5122-5139. doi: 10.1523/JNEUROSCI.3652-17.2018. Epub 2018 May 14.
9
Conditioning lesions enhance growth state only in sensory neurons lacking calcitonin gene-related peptide and isolectin B4-binding.
Neuroscience. 2010 Mar 10;166(1):107-21. doi: 10.1016/j.neuroscience.2009.12.019. Epub 2009 Dec 16.

引用本文的文献

2
Modulation of pain by ketones: a mini-review.
Am J Physiol Cell Physiol. 2025 Jul 1;329(1):C31-C37. doi: 10.1152/ajpcell.00305.2025. Epub 2025 May 28.
3
ATP-gated potassium channels contribute to ketogenic diet-mediated analgesia in mice.
Neurobiol Pain. 2023 Jul 3;14:100138. doi: 10.1016/j.ynpai.2023.100138. eCollection 2023 Aug-Dec.
4
Ketolysis is required for the proper development and function of the somatosensory nervous system.
Exp Neurol. 2023 Jul;365:114428. doi: 10.1016/j.expneurol.2023.114428. Epub 2023 Apr 24.
5
Ketolysis is Required for the Proper Development and Function of the Somatosensory Nervous System.
bioRxiv. 2023 Mar 30:2023.01.11.523492. doi: 10.1101/2023.01.11.523492.
6
Both age and social environment shape the phenotype of ant workers.
Sci Rep. 2023 Jan 5;13(1):186. doi: 10.1038/s41598-022-26515-1.
7
Emerging Nonpharmacologic Interventions to Treat Diabetic Peripheral Neuropathy.
Antioxid Redox Signal. 2023 May;38(13-15):989-1000. doi: 10.1089/ars.2022.0158. Epub 2023 Feb 7.
8
Potential for Ketotherapies as Amyloid-Regulating Treatment in Individuals at Risk for Alzheimer's Disease.
Front Neurosci. 2022 Jun 16;16:899612. doi: 10.3389/fnins.2022.899612. eCollection 2022.
9
Nutritional Impact on Metabolic Homeostasis and Brain Health.
Front Neurosci. 2022 Jan 27;15:767405. doi: 10.3389/fnins.2021.767405. eCollection 2021.
10
The Role of Dietary Nutrients in Peripheral Nerve Regeneration.
Int J Mol Sci. 2021 Jul 10;22(14):7417. doi: 10.3390/ijms22147417.

本文引用的文献

1
Intrinsic Activity of C57BL/6 Substrains Associates with High-Fat Diet-Induced Mechanical Sensitivity in Mice.
J Pain. 2018 Nov;19(11):1285-1295. doi: 10.1016/j.jpain.2018.05.005. Epub 2018 May 25.
2
A ketogenic diet reduces metabolic syndrome-induced allodynia and promotes peripheral nerve growth in mice.
Exp Neurol. 2018 Aug;306:149-157. doi: 10.1016/j.expneurol.2018.05.011. Epub 2018 May 17.
3
Modulation of diet-induced mechanical allodynia by metabolic parameters and inflammation.
J Peripher Nerv Syst. 2017 Mar;22(1):39-46. doi: 10.1111/jns.12199.
5
Peripheral neuropathy: clinical and electrophysiological considerations.
Neuroimaging Clin N Am. 2014 Feb;24(1):49-65. doi: 10.1016/j.nic.2013.03.023. Epub 2013 May 25.
6
Localization of mitochondrial carnitine/acylcarnitine translocase in sensory neurons from rat dorsal root ganglia.
Neurochem Res. 2013 Dec;38(12):2535-41. doi: 10.1007/s11064-013-1168-z. Epub 2013 Oct 9.
7
Chewing the fat: genetic approaches to model dyslipidemia-induced diabetic neuropathy in mice.
Exp Neurol. 2013 Oct;248:504-8. doi: 10.1016/j.expneurol.2013.07.016. Epub 2013 Aug 8.
8
Exercise-mediated improvements in painful neuropathy associated with prediabetes in mice.
Pain. 2013 Dec;154(12):2658-2667. doi: 10.1016/j.pain.2013.07.052. Epub 2013 Aug 6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验