短期有氧运动以性别依赖的方式防止老年骨骼肌糖皮质激素性肌病特征的发展。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Journal of Physiology-London Pub Date : 2025-01-01 Epub Date: 2024-06-11 DOI:10.1113/JP286334
Grant R Laskin, Liliana I Rentería, Judy M Muller-Delp, Jeong-Su Kim, P Bryant Chase, Hyun Seok Hwang, Bradley S Gordon
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引用次数: 0

摘要

老年人易受糖皮质激素诱导的肌肉萎缩和无力的影响,性别可能会影响他们对这些影响的易感性。有氧运动可以减少糖皮质激素诱导的年轻啮齿动物肌肉萎缩。然而,有氧运动能否预防糖皮质激素导致的老年肌肉肌病尚不清楚。本研究的目的是确定性别在多大程度上影响糖皮质激素性肌病在老年肌肉中的发生,并确定有氧运动训练在多大程度上保护肌肉不发生肌病。将24个月大的雌性(30只)和雄性(33只)小鼠随机分为静坐组或有氧运动组。在各自的组别中,小鼠随机接受地塞米松(DEX)或生理盐水的每日治疗。完成治疗后,原位评估肱三头肌复合体的收缩特性。地塞米松略微降低了男女肌肉质量和可溶性蛋白含量,但只有女性的肌肉质量和可溶性蛋白含量在有氧运动中有所降低。DEX只增加了女性的胫下肌力和肌力发展速度,而有氧运动对其没有影响。在使用 DEX 后,两性的肌肉疲劳程度都较高,但有氧运动仅能防止女性产生疲劳。肌肉功能对DEX处理的性别差异与肌肉中与钙处理、线粒体质量控制、活性氧生成和糖皮质激素受体相关的蛋白质含量的性别差异一致。这些发现确定了老年骨骼肌生理机能在糖皮质激素治疗下发生的几种重要的性别双态变化,并确定了短期有氧运动对这些变化的保护能力。关键点:糖皮质激素对老年骨骼肌生理机能的影响存在性别差异。糖皮质激素诱导的老年肌肉收缩特性变化与钙处理蛋白含量的性别差异相吻合。有氧运动仅在老年女性中能防止糖皮质激素引起的疲劳,这与线粒体质量控制蛋白和糖皮质激素受体含量的差异相吻合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Short-term aerobic exercise prevents development of glucocorticoid myopathic features in aged skeletal muscle in a sex-dependent manner.

Older adults are vulnerable to glucocorticoid-induced muscle atrophy and weakness, with sex potentially influencing their susceptibility to those effects. Aerobic exercise can reduce glucocorticoid-induced muscle atrophy in young rodents. However, it is unknown whether aerobic exercise can prevent glucocorticoid myopathy in aged muscle. The objectives of this study were to define the extent to which sex influences the development of glucocorticoid myopathy in aged muscle, and to determine the extent to which aerobic exercise training protects against myopathy development. Twenty-four-month-old female (n = 30) and male (n = 33) mice were randomized to either sedentary or aerobic exercise groups. Within their respective groups, mice were randomized to either daily treatment with dexamethasone (DEX) or saline. Upon completing treatments, the contractile properties of the triceps surae complex were assessed in situ. DEX marginally lowered muscle mass and soluble protein content in both sexes, which was attenuated by aerobic exercise only in females. DEX increased sub-tetanic force and rate of force development only in females, which was not influenced by aerobic exercise. Muscle fatigue was higher in both sexes following DEX, but aerobic exercise prevented fatigue induction only in females. The sex-specific differences to muscle function in response to DEX treatment coincided with sex-specific changes to the content of proteins related to calcium handling, mitochondrial quality control, reactive oxygen species production, and glucocorticoid receptor in muscle. These findings define several important sexually dimorphic changes to aged skeletal muscle physiology in response to glucocorticoid treatment and define the capacity of short-term aerobic exercise to protect against those changes. KEY POINTS: There are sexually dimorphic effects of glucocorticoids on aged skeletal muscle physiology. Glucocorticoid-induced changes to aged muscle contractile properties coincide with sex-specific differences in the content of calcium handling proteins. Aerobic exercise prevents glucocorticoid-induced fatigue only in aged females and coincides with differences in the content of mitochondrial quality control proteins and glucocorticoid receptors.

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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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