A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice

Author:

Petr Michael A12,Alfaras Irene2,Krawcyzk Melissa3,Bair Woei-Nan24,Mitchell Sarah J2,Morrell Christopher H3,Studenski Stephanie A25,Price Nathan L26789,Fishbein Kenneth W10,Spencer Richard G10,Scheibye-Knudsen Morten1,Lakatta Edward G3,Ferrucci Luigi2ORCID,Aon Miguel A23,Bernier Michel2ORCID,de Cabo Rafael2ORCID

Affiliation:

1. Center for Healthy Aging, ICMM, University of Copenhagen, Copenhagen, Denmark

2. Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, United States

3. Laboratory of Cardiovascular Science, National Institute on Aging, NIH, Baltimore, United States

4. Department of Physical Therapy, University of Sciences, Philadelphia, United States

5. Division of Geriatric Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, United States

6. Integrative Cell Signaling and Neurobiology of Metabolism Program, Yale University School of Medicine, New Haven, United States

7. Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, United States

8. Department of Comparative Medicine, Yale University School of Medicine, New Haven, United States

9. Department of Pathology, Yale University School of Medicine, New Haven, United States

10. Laboratory of Clinical Investigation, National Institute on Aging, NIH, Baltimore, United States

Abstract

Aging is associated with distinct phenotypical, physiological, and functional changes, leading to disease and death. The progression of aging-related traits varies widely among individuals, influenced by their environment, lifestyle, and genetics. In this study, we conducted physiologic and functional tests cross-sectionally throughout the entire lifespan of male C57BL/6N mice. In parallel, metabolomics analyses in serum, brain, liver, heart, and skeletal muscle were also performed to identify signatures associated with frailty and age-dependent functional decline. Our findings indicate that declines in gait speed as a function of age and frailty are associated with a dramatic increase in the energetic cost of physical activity and decreases in working capacity. Aging and functional decline prompt organs to rewire their metabolism and substrate selection and toward redox-related pathways, mainly in liver and heart. Collectively, the data provide a framework to further understand and characterize processes of aging at the individual organism and organ levels.

Funder

National Institute on Aging

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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