Limanaqi Fiona, Ferri Evelyn, Ogno Pasquale, Guerini Franca Rosa, Mihali Gabriela Alexandra, Lucchi Tiziano, Clerici Mario, Fenoglio Chiara, D'Andrea Laura, Marcello Elena, Biasin Mara, Arosio Beatrice
Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
IRCCS Fondazione Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Aging Cell. 2025 Jun;24(6):e70029. doi: 10.1111/acel.70029. Epub 2025 Mar 4.
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.
体育锻炼与更健康的衰老轨迹相关,有可能预防或减轻与年龄相关的衰退。这是通过一个复杂但特征不明的多器官相互作用网络实现的,该网络涉及线粒体、炎症以及细胞死亡/存活途径。在此,我们对身体虚弱(n = 16,平均年龄81.4 ± 5.6岁)和身体强健(n = 50,平均年龄73.6 ± 4.7岁)的老年人进行了为期12周的VIVIFRAIL多组分运动方案的综合评估。在方案实施前(T0)和实施后(T1),评估了功能结果,并对线粒体、炎症、凋亡和神经肌肉介质进行了详细的探索性分析,涉及它们的血浆/血清浓度和/或外周血单个核细胞(PBMC)的mRNA表达。除了两组在功能上都有显著改善外,我们的研究结果突出了关键生物途径的独特和重叠调节。两组均显示线粒体完整性/周转率得到改善(mt-ND1上调、TFAM和ULK1下调)、抗炎反应(IL10和TGF-B上调,IL6/IL10 mRNA比值下调),以及细胞损伤/凋亡减少(血浆ccf-nDNA减少、BAX下调、BCL-2/BAX比值上调)。强健受试者的血浆ccf-mtDNA显著降低,而虚弱受试者的血浆IL6和IL6/IL10比值则独特地降低。身体改善与生物途径变化之间的Spearman相关性还表明,不同的适应机制不仅受实际年龄影响,还受虚弱状态影响。总之,本研究证实了体育活动对老年人群的益处,并为线粒体-炎症轴的特定生物介质作为此类效应的关键参与者提供了新的见解。此外,我们的研究结果确立了PBMC作为监测衰老生物轨迹和促进健康生活方式干预的有价值工具。