Aging Skeletal Muscle Plasticity in Exercise and Injury

dc.creatorBrightwell, Camille R.
dc.date.accessioned2024-03-11T21:37:07Z
dc.date.available2024-03-11T21:37:07Z
dc.date.created2021-05
dc.date.issuedMay 2021
dc.date.submittedMay 2021
dc.date.updated2024-03-11T21:37:08Z
dc.description.abstractSarcopenia—progressive loss of muscle mass and strength—diminishes quality of life and longevity. In addition to progressive atrophy, older adults exhibit impaired regeneration after muscular injury. Activity of muscle stem cells, termed satellite cells, is dysregulated with aging which impairs skeletal muscle remodeling and limits plasticity of aged muscle. Aim 1 (Chapter 2) of this dissertation seeks to clarify the debated requirement of satellite cells for overload-induced hypertrophy in aging muscle via a common surgical overload model, with the original hypothesis that while aging satellite cells contribute to overload-induced hypertrophy to mitigate sarcopenia, growth can occur in the absence of satellite cells via expansion of the myonuclear domain. In light of Aim 1 results demonstrating no overload-induced hypertrophy in aging skeletal muscle with surgical overload, Aim 2 (Chapter 3) examines the efficacy of a novel and translatable murine resistance exercise model to elicit satellite cell expansion with myonuclear accretion and hypertrophy in aging skeletal muscle, with the hypothesis that this novel exercise model would result in expansion of the satellite cell pool along with hypertrophy not observed in old mice with the surgical overload model. Indeed, PoWeR (Progressive Weighted wheel Running) elicited hypertrophy in old mice, likely supported by a robust angiogenic response in hind limb muscles. Lastly, Aim 3 (Chapter 4) examines the efficacy of a novel NNMT inhibitor to enhance regeneration of aging skeletal muscle after injury by enhancement of satellite cell proliferation and fusion to myofibers, confirming the hypothesis that NNMT inhibition would rescue age-related deficits in satellite cell activity to promote superior regeneration of muscular injury of old mice.
dc.format.mimetypeapplication/pdf
dc.identifier.uri
dc.identifier.urihttps://hdl.handle.net/2152.3/12325
dc.subjectBiology, Cell
dc.subjectBiology, Animal Physiology
dc.subject.othersarcopenia, satellite cells
dc.titleAging Skeletal Muscle Plasticity in Exercise and Injury
dc.typeThesis
dc.type.materialtext
local.embargo.lift05/01/2024
local.embargo.terms05/01/2024
thesis.degree.departmentCell Biology
thesis.degree.grantorThe University of Texas Medical Branch at Galveston
thesis.degree.nameCell Biology (Doctoral)

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