老年男性和女性有丝分裂调节药物的使用和骨骼肌生物能量学:肌肉、活动能力和衰老的研究。

Howard J Phang, Jaclyn Bergstrom, Rabia S Atayee, Laura A Hart, Peggy M Cawthon, Terri Blackwell, Philip A Kramer, Giovanna Distefano, Erin E Kershaw, Steven R Cummings, Anthony J A Molina
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引用次数: 0

摘要

背景:尽管在老年人中“线粒体调节”药物的使用非常普遍,但药物诱导的人类线粒体功能调节的潜在影响仍不清楚。虽然这些药物,如他汀类药物和二甲双胍,已经在体外对其对线粒体功能的影响进行了广泛的表征,但对人类的影响要复杂得多,而且知之甚少。方法:本研究使用肌肉、运动和衰老研究(SOMMA)的数据来评估有丝分裂调节药物的使用与骨骼肌生物能量能力的关系,通过体外高分辨率呼吸法和体内磷磁共振波谱法在健康老年人中测量。结果:我们发现有丝分裂调节药物的使用与男性较低的最大复合体i和ii支持氧化磷酸化(Max OXPHOS)、最大电子传递系统容量(Max ETS)和最大ATP生产能力(ATP Max)有关,但与女性无关。我们还发现这与使用的药物数量有关,其中较高的有丝分裂调节药物负荷与较低的最大OXPHOS、最大ETS和ATP Max相关。结论:我们的研究结果为使用线粒体调节药物的潜在临床效果提供了更深入的了解,并强调了在随机试验中测试这些药物对线粒体功能影响的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mito-Modulatory Medication Use and Skeletal Muscle Bioenergetics Among Older Men and Women: the Study of Muscle, Mobility and Aging.

Background: The potential impacts of drug-induced modulation of mitochondrial function in humans remain unclear despite the high prevalence of "mito-modulatory" medication use among older adults. While these medications, such as statins and metformin, have undergone extensive characterization of their effects on mitochondrial function in vitro, the effects in humans are far more complex and poorly understood.

Methods: This study uses data from the Study of Muscle, Mobility and Aging (SOMMA) to evaluate how mito-modulatory medication use is related to skeletal muscle bioenergetic capacity, measured by ex vivo high-resolution respirometry and in vivo phosphorus magnetic resonance spectroscopy in healthy older adults.

Results: We found that mito-modulatory medication use was related to lower maximal complex I&II supported oxidative phosphorylation (Max OXPHOS), maximal electron transfer system capacity (Max ETS), and maximal ATP production capacity (ATP Max) in men, but not in women. We also found this to be dependent on the number of medications used, in which higher mito-modulatory medication load was associated with lower Max OXPHOS, Max ETS, and ATP Max.

Conclusions: Our results provide greater insight into the potential clinical effects of mito-modulatory medication use and highlight the need to test the impact of these medications on mitochondrial function in randomized trials.

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