Effects of the VIVIFRAIL Exercise Protocol on Circulatory and Intracellular Peripheral Mediators Bridging Mitochondrial Dynamics and Inflammation in Robust and Frail Older People

IF 7.1 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Aging Cell Pub Date : 2025-03-04 DOI:10.1111/acel.70029
Fiona Limanaqi, Evelyn Ferri, Pasquale Ogno, Franca Rosa Guerini, Gabriela Alexandra Mihali, Tiziano Lucchi, Mario Clerici, Chiara Fenoglio, Laura D'Andrea, Elena Marcello, Mara Biasin, Beatrice Arosio
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Abstract

Physical exercise has been associated with healthier aging trajectories, potentially preventing or mitigating age-related declines. This occurs through a complex, yet poorly characterized network of multi-organ interactions involving mitochondrial, inflammatory, and cell death/survival pathways. Here, we comprehensively evaluated the 12-week VIVIFRAIL multicomponent exercise protocol in physically frail (n = 16, mean age 81.4 ± 5.6) and robust (n = 50, mean-age 73.6 ± 4.7) old individuals. Before (T0) and after (T1) the protocol, functional outcomes were assessed alongside a detailed exploratory analysis of mitochondrial, inflammatory, apoptotic, and neuro-muscular mediators concerning their plasmatic/serum concentrations, and/or mRNA expression from peripheral blood mononuclear cells (PBMCs). Besides significant functional improvements across both groups, our findings highlighted unique and overlapping modulations of key biological pathways. Both groups showed refined mitochondrial integrity/turnover (upregulated mt-ND1, downregulated TFAM, and ULK1), anti-inflammatory responses (upregulated IL10, and TGF-B, and downregulated IL6/IL10 mRNA ratio), as well as reduced cellular damage/apoptosis (reduced plasmatic ccf-nDNA, downregulated BAX, and upregulated BCL-2/BAX ratio). Plasmatic ccf-mtDNA was significantly reduced in robust subjects, while plasmatic IL6 and IL6/IL10 ratio were reduced in frail subjects uniquely. Spearman correlations between physical improvements and biological pathway variations also suggested different adaptation mechanisms influenced not only by chronological age but also by frailty status. In conclusion, this study confirms the benefits of physical activity in the older population and provides novel insights into specific biological mediators of the mitochondria-inflammation axis as key players in such effects. Moreover, our findings establish PBMCs as a valuable tool for monitoring the biological trajectories of aging and health-promoting lifestyle interventions.

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在健壮和虚弱的老年人中,vivi虚弱运动方案对连接线粒体动力学和炎症的循环和细胞内周围介质的影响。
体育锻炼与健康的衰老轨迹有关,有可能预防或减轻与年龄有关的衰退。这是通过一个复杂的,但尚未明确的多器官相互作用网络发生的,涉及线粒体、炎症和细胞死亡/生存途径。在这里,我们对身体虚弱(n = 16,平均年龄81.4±5.6)和健壮(n = 50,平均年龄73.6±4.7)的老年人进行了为期12周的vivi虚弱多组分运动方案的综合评估。在治疗前(T0)和治疗后(T1),对功能结果进行评估,同时对线粒体、炎症、凋亡和神经肌肉介质的血浆/血清浓度和/或外周血单核细胞(PBMCs) mRNA表达进行详细的探索性分析。除了两组显著的功能改善外,我们的发现还强调了关键生物途径的独特和重叠调节。两组均表现出改善的线粒体完整性/更新(mt-ND1上调,TFAM和ULK1下调),抗炎反应(IL10和TGF-B上调,IL6/IL10 mRNA比例下调),以及细胞损伤/凋亡减少(血浆ccf-nDNA减少,BAX下调,BCL-2/BAX比例上调)。体质强健的受试者血浆ccf-mtDNA显著降低,而体质虚弱的受试者血浆IL6和IL6/IL10比值降低。生理改善和生物通路变异之间的Spearman相关性还表明,不同的适应机制不仅受实足年龄的影响,还受虚弱状态的影响。总之,这项研究证实了体育锻炼对老年人的好处,并为线粒体-炎症轴的特定生物介质作为这种影响的关键参与者提供了新的见解。此外,我们的研究结果建立了pbmc作为监测衰老和促进健康的生活方式干预的生物轨迹的有价值的工具。
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来源期刊
Aging Cell
Aging Cell 生物-老年医学
CiteScore
14.40
自引率
2.60%
发文量
212
审稿时长
8 weeks
期刊介绍: Aging Cell, an Open Access journal, delves into fundamental aspects of aging biology. It comprehensively explores geroscience, emphasizing research on the mechanisms underlying the aging process and the connections between aging and age-related diseases.
期刊最新文献
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