IF 4.7 2区 医学 Q1 NEUROSCIENCES
Stephanie R Mattina, Sean Y Ng, Andrew I Mikhail, Derek W Stouth, Cora E Jornacion, Irena A Rebalka, Thomas J Hawke, Vladimir Ljubicic
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引用次数: 0

摘要

杜兴氏肌肉萎缩症(DMD)的特点是进行性肌肉萎缩和无力。规定的适度运动对患者有益,但由于肌营养不良症肌肉易受损,因此仍存在一些问题。自愿轮跑(VWR)是一种自我调节的运动形式,可改善典型的 C57.mdx DMD 小鼠模型的肌肉健康状况。本研究的目的是调查 VWR 对更严重和临床相关的 D2.mdx 小鼠的影响。雄性 D2.mdx 小鼠被分配到静坐组(D2.mdx SED)或 VWR 组,为期 8-10 周,而 DBA/2J 野生型小鼠则作为健康的静坐对照组(WT SED)。与低量跑步者(D2.mdx Low VWR;0.46 ± 0.31 km/天)和SED动物相比,高量跑步的D2.mdx动物(D2.mdx High VWR;1.84 ± 0.84 km/天)的选择性骨骼肌质量和体内外产力均有所提高。与D2.mdx SED小鼠相比,VWR并没有加重肌营养不良,反而减轻了纤维化特征。此外,还观察到 VWR 诱导的向更缓慢的氧化表型的转变。与 WT SED 小鼠相比,D2.mdx SED 动物的线粒体呼吸减少,但在低度和高度 VWR 之后,线粒体呼吸得到部分恢复。最后,在 VWR 之后观察到线粒体蛋白的表达呈剂量依赖性增加,而线粒体融合的标记物在 D2.mdx High VWR 小鼠中尤其升高。我们的研究结果表明,VWR 可增强 D2.mdx 动物的肌肉和线粒体生物学特性,并进一步支持运动对 DMD 患者的治疗作用。关键点杜兴氏肌营养不良症(DMD)是一种以肌肉无力和萎缩为特征的限制性神经肌肉疾病。肌营养不良症患者的骨骼肌和心肌质量受到损害。运动能促进健康人和轻度肌营养不良小鼠模型的功能和分子适应。然而,还需要研究运动对更严重和临床相关的 DMD 模型的影响。相对大量的自愿轮跑(VWR)增强了D2.mdx小鼠的选择性肌肉质量和肌肉功能,而不会加重肌营养不良的病理变化。与久坐不动的小鼠相比,自愿运动可使营养不良骨骼肌线粒体呼吸正常化,并提高线粒体含量。与健康和萎缩性静坐动物以及运动量较小的D2.mdx小鼠相比,较高剂量的VWR可增加细胞器融合蛋白的表达。我们的研究结果从一个严重的临床前模型中提供了证据,表明自愿运动可能是一种安全、有效的基于生活方式的DMD干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Volitional exercise elicits physiological and molecular improvements in the severe D2.mdx mouse model of Duchenne muscular dystrophy.

Duchenne muscular dystrophy (DMD) is characterized by progressive muscle wasting and weakness. Prescribed moderate exercise in patients is beneficial, but concerns remain due to the vulnerability of dystrophic muscle to damage. Voluntary wheel running (VWR) is a self-regulated form of exercise that improves muscle health in the typical C57.mdx mouse model of DMD. The purpose of the current study was to investigate the impact of VWR in more severe and clinically relevant D2.mdx mice. Male D2.mdx animals were assigned to a sedentary (D2.mdx SED) or VWR group for 8-10 weeks, whereas DBA/2J wild-type mice served as healthy, sedentary controls (WT SED). Selective skeletal muscle mass and ex vivo force generation were elevated in D2.mdx animals that ran a relatively high volume (D2.mdx High VWR; 1.84 ± 0.84 km/day) compared to low-volume runners (D2.mdx Low VWR; 0.46 ± 0.31 km/day) and SED counterparts. VWR did not exacerbate the dystrophy, and instead attenuated the fibrotic profile compared to D2.mdx SED mice. A VWR-induced shift towards a more slow, oxidative phenotype was also observed. Mitochondrial respiration was reduced in D2.mdx SED animals versus WT SED mice but was partially restored following both Low and High VWR. Finally, a dose-dependent increase in the expression of mitochondrial proteins was observed following VWR, whereas markers of mitochondrial fusion were particularly elevated in D2.mdx High VWR mice. Our results indicate that VWR enhances muscle and mitochondrial biology in D2.mdx animals and further supports the therapeutic role of exercise for DMD patients. KEY POINTS: Duchenne muscular dystrophy (DMD) is a life-limiting neuromuscular disorder characterized by muscle weakness and wasting. Skeletal and cardiac muscle quality is compromised in the dystrophic condition. Exercise promotes functional and molecular adaptations in healthy individuals and mild dystrophic mouse models. However, the effects of exercise in more severe and clinically relevant models of DMD require investigation. A relatively high volume of voluntary wheel running (VWR) augmented selective muscle mass and muscle function without exacerbating the dystrophic pathology in D2.mdx mice. Volitional exercise normalized dystrophic skeletal muscle mitochondrial respiration and upregulated mitochondrial content compared to sedentary counterparts. A higher dose of VWR increased organelle fusion protein expression compared to both healthy and dystrophic sedentary animals, as well as D2.mdx mice that ran lower volumes. Our results provide evidence from a severe preclinical model that volitional exercise may be a safe and efficacious lifestyle-based intervention for DMD.

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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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