生酮饮食和有氧运动对模拟微重力小鼠骨骼肌纤维重塑和代谢适应的联合影响。

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Metabolites Pub Date : 2025-04-13 DOI:10.3390/metabo15040270
Jun Chen, Wenjiong Li, Liang Yu, Bowei Zhang, Zhili Li, Peng Zou, Bai Ding, Xiaoqian Dai, Qirong Wang
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引用次数: 0

摘要

目的:长期微重力环境通过引发纤维型转变和代谢失调损害骨骼肌内稳态。虽然运动和营养干预可以缓解废用性萎缩,但它们在微重力条件下的协同效应仍然不清楚。本研究研究了8周生酮饮食结合有氧运动对后肢无负重小鼠肌纤维重塑和代谢适应的影响。方法:将7周龄雄性C57BL/6J小鼠随机分为正常饮食控制组(NC)、正常饮食加后肢卸荷组(NH)、正常饮食加后肢卸荷组(NHE)、生酮饮食控制组(KC)、生酮饮食加后肢卸荷组(KH)和生酮饮食加后肢卸荷组(KHE)。在干预的最后两周,后肢卸载应用于模拟微重力。有氧运动组进行中等强度的跑步(12米/分钟,60分钟/天,6天/周),持续8周。每周测量体重、血酮和血糖水平。干预后评估包括呼吸交换率(RER)、详尽运动表现测试和血液代谢参数的生化分析。免疫荧光染色评估骨骼肌纤维类型组成,油红O染色评估脂质沉积,周期性酸-希夫(PAS)染色分析糖原含量,实时荧光定量PCR (RT-qPCR)测定基因表达。结果:后肢卸荷显著降低小鼠体重,诱发肌肉萎缩,降低运动耐力。然而,KD和有氧运动的结合显著减轻了这些不良反应,氧化肌纤维(MyHC-I)的比例增加,糖酵解纤维(MyHC-IIb)的比例减少。此外,这种联合干预上调了脂质代谢相关基因的表达,包括CPT-1b、HADH、PGC-1α和FGF21,增强了脂质代谢和酮的利用。这些代谢适应与运动表现的改善相对应,与其他后肢卸载组相比,KHE组的疲劳时间增加。结论:生酮饮食和有氧运动的结合有效改善了模拟微重力诱导的骨骼肌萎缩和耐力损伤,主要是通过促进纤维类型从MyHC-IIb向MyHC-I的转变,并增强脂质代谢基因(CPT-1b、HADH和PGC-1α)的表达。这些发现强调了在模拟微重力条件下,饮食和运动联合干预减轻肌肉萎缩的潜在治疗价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined Effects of Ketogenic Diet and Aerobic Exercise on Skeletal Muscle Fiber Remodeling and Metabolic Adaptation in Simulated Microgravity Mice.

Objective: Prolonged microgravity environments impair skeletal muscle homeostasis by triggering fiber-type transitions and metabolic dysregulation. Although exercise and nutritional interventions may alleviate disuse atrophy, their synergistic effects under microgravity conditions remain poorly characterized. This study investigated the effects of an 8-week ketogenic diet combined with aerobic exercise in hindlimb-unloaded mice on muscle fiber remodeling and metabolic adaptation. Methods: Seven-week-old male C57BL/6J mice were randomly divided into six groups: normal diet control (NC), normal diet with hindlimb unloading (NH), normal diet with hindlimb unloading and exercise (NHE), ketogenic diet control (KC), ketogenic diet with hindlimb unloading (KH), and ketogenic diet with hindlimb unloading and exercise (KHE). During the last two weeks of intervention, hindlimb unloading was applied to simulate microgravity. Aerobic exercise groups performed moderate-intensity treadmill running (12 m/min, 60 min/day, and 6 days/week) for 8 weeks. Body weight, blood ketone, and glucose levels were measured weekly. Post-intervention assessments included the respiratory exchange ratio (RER), exhaustive exercise performance tests, and biochemical analyses of blood metabolic parameters. The skeletal muscle fiber-type composition was evaluated via immunofluorescence staining, lipid deposition was assessed using Oil Red O staining, glycogen content was analyzed by Periodic Acid-Schiff (PAS) staining, and gene expression was quantified using quantitative real-time PCR (RT-qPCR). Results: Hindlimb unloading significantly decreased body weight, induced muscle atrophy, and reduced exercise endurance in mice. However, the combination of KD and aerobic exercise significantly attenuated these adverse effects, as evidenced by increased proportions of oxidative muscle fibers (MyHC-I) and decreased proportions of glycolytic fibers (MyHC-IIb). Additionally, this combined intervention upregulated the expression of lipid metabolism-associated genes, including CPT-1b, HADH, PGC-1α, and FGF21, enhancing lipid metabolism and ketone utilization. These metabolic adaptations corresponded with improved exercise performance, demonstrated by the increased time to exhaustion in the KHE group compared to other hindlimb unloading groups. Conclusions: The combination of a ketogenic diet and aerobic exercise effectively ameliorates simulated microgravity-induced skeletal muscle atrophy and endurance impairment, primarily by promoting a fiber-type transition from MyHC-IIb to MyHC-I and enhancing lipid metabolism gene expression (CPT-1b, HADH, and PGC-1α). These findings underscore the potential therapeutic value of combined dietary and exercise interventions for mitigating muscle atrophy under simulated microgravity conditions.

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来源期刊
Metabolites
Metabolites Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
5.70
自引率
7.30%
发文量
1070
审稿时长
17.17 days
期刊介绍: Metabolites (ISSN 2218-1989) is an international, peer-reviewed open access journal of metabolism and metabolomics. Metabolites publishes original research articles and review articles in all molecular aspects of metabolism relevant to the fields of metabolomics, metabolic biochemistry, computational and systems biology, biotechnology and medicine, with a particular focus on the biological roles of metabolites and small molecule biomarkers. Metabolites encourages scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on article length. Sufficient experimental details must be provided to enable the results to be accurately reproduced. Electronic material representing additional figures, materials and methods explanation, or supporting results and evidence can be submitted with the main manuscript as supplementary material.
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