The clinical impact and biological mechanisms of skeletal muscle aging. 2019

Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, MN, United States of America; Robert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN, United States of America.

Skeletal muscle is a highly plastic tissue that remarkably adapts to diverse stimuli including exercise, injury, disuse, and, as discussed here, aging. Humans achieve peak skeletal muscle mass and strength in mid-life and then experience a progressive decline of up to 50% by the ninth decade. The loss of muscle mass and function with aging is a phenomenon termed sarcopenia. It is evidenced by the loss and atrophy of muscle fibers and the concomitant accretion of fat and fibrous tissue. Sarcopenia has been recognized as a key driver of limitations in physical function and mobility, but is perhaps less appreciated for its role in age-related metabolic dysfunction and loss of organismal resilience. Similar to other tissues, muscle is prone to multiple forms of age-related molecular and cellular damage, including disrupted protein turnover, impaired regenerative capacity, cellular senescence, and mitochondrial dysfunction. The objective of this review is to highlight the clinical consequences of skeletal muscle aging, and provide insights into potential biological mechanisms. In light of population aging, strategies to improve muscle health in older adults promise to have a profound public health impact.

UI MeSH Term Description Entries
D008928 Mitochondria Semiautonomous, self-reproducing organelles that occur in the cytoplasm of all cells of most, but not all, eukaryotes. Each mitochondrion is surrounded by a double limiting membrane. The inner membrane is highly invaginated, and its projections are called cristae. Mitochondria are the sites of the reactions of oxidative phosphorylation, which result in the formation of ATP. They contain distinctive RIBOSOMES, transfer RNAs (RNA, TRANSFER); AMINO ACYL T RNA SYNTHETASES; and elongation and termination factors. Mitochondria depend upon genes within the nucleus of the cells in which they reside for many essential messenger RNAs (RNA, MESSENGER). Mitochondria are believed to have arisen from aerobic bacteria that established a symbiotic relationship with primitive protoeukaryotes. (King & Stansfield, A Dictionary of Genetics, 4th ed) Mitochondrial Contraction,Mitochondrion,Contraction, Mitochondrial,Contractions, Mitochondrial,Mitochondrial Contractions
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000375 Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. Senescence,Aging, Biological,Biological Aging
D013234 Stem Cells Relatively undifferentiated cells that retain the ability to divide and proliferate throughout postnatal life to provide progenitor cells that can differentiate into specialized cells. Colony-Forming Units,Mother Cells,Progenitor Cells,Colony-Forming Unit,Cell, Mother,Cell, Progenitor,Cell, Stem,Cells, Mother,Cells, Progenitor,Cells, Stem,Colony Forming Unit,Colony Forming Units,Mother Cell,Progenitor Cell,Stem Cell
D016922 Cellular Senescence Process by which cells irreversibly stop dividing and enter a state of permanent growth arrest without undergoing CELL DEATH. Senescence can be induced by DNA DAMAGE or other cellular stresses, such as OXIDATIVE STRESS. Aging, Cell,Cell Aging,Cell Senescence,Replicative Senescence,Senescence, Cellular,Senescence, Replicative,Cell Ageing,Cellular Ageing,Cellular Aging,Ageing, Cell,Ageing, Cellular,Aging, Cellular,Senescence, Cell
D018482 Muscle, Skeletal A subtype of striated muscle, attached by TENDONS to the SKELETON. Skeletal muscles are innervated and their movement can be consciously controlled. They are also called voluntary muscles. Anterior Tibial Muscle,Gastrocnemius Muscle,Muscle, Voluntary,Plantaris Muscle,Skeletal Muscle,Soleus Muscle,Muscle, Anterior Tibial,Muscle, Gastrocnemius,Muscle, Plantaris,Muscle, Soleus,Muscles, Skeletal,Muscles, Voluntary,Skeletal Muscles,Tibial Muscle, Anterior,Voluntary Muscle,Voluntary Muscles

Related Publications

Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
January 2014, Frontiers in aging neuroscience,
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
March 2016, Ageing research reviews,
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
October 2000, Drugs & aging,
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
November 2013, Disease models & mechanisms,
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
June 2023, The journals of gerontology. Series A, Biological sciences and medical sciences,
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
January 2001, Frontiers in bioscience : a journal and virtual library,
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
January 2017, Clinical calcium,
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
June 2022, Molecular and cellular biochemistry,
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
April 2006, Journal of applied physiology (Bethesda, Md. : 1985),
Zaira Aversa, and Xu Zhang, and Roger A Fielding, and Ian Lanza, and Nathan K LeBrasseur
September 2016, Free radical biology & medicine,
Copied contents to your clipboard!