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

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 path...

Full description

Saved in:
Bibliographic Details
Published inAging cell Vol. 24; no. 6; pp. e70029 - n/a
Main Authors 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
Format Journal Article
LanguageEnglish
Published England John Wiley & Sons, Inc 01.06.2025
John Wiley and Sons Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary: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. Physical activity promotes functional improvements in both robust and physically frail older adults, driven by distinct adaptation mechanisms in the mitochondria‐inflammation axis that are influenced by age and frailty status.
Bibliography:Fiona Limanaqi and Evelyn Ferri First authors equally contributed.
Mara Biasin and Beatrice Arosio Senior authors equally contributed.
Funding
This work was supported by Fondazione Cariplo, 2017‐0622, by grants from Fondazione Romeo and Enrica Invernizzi, and by the Italian Ministry of Health, under the Aging Network of Italian Research Hospitals (IRCCS), RCR‐2022‐23682286 (Ricerca Corrente Reti 2022).
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
Funding: This work was supported by Fondazione Cariplo, 2017‐0622, by grants from Fondazione Romeo and Enrica Invernizzi, and by the Italian Ministry of Health, under the Aging Network of Italian Research Hospitals (IRCCS), RCR‐2022‐23682286 (Ricerca Corrente Reti 2022).
ISSN:1474-9718
1474-9726
1474-9726
DOI:10.1111/acel.70029