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Aging of the musculoskeletal system: How the loss of estrogen impacts muscle strength

Skeletal muscle weakness occurs with aging and in females this is compounded by the loss of estrogen with ovarian failure. Estrogen deficiency mediates decrements in muscle strength from both inadequate preservation of skeletal muscle mass and decrements in the quality of the remaining skeletal musc...

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Bibliographic Details
Published in:Bone (New York, N.Y.) N.Y.), 2019-06, Vol.123, p.137-144
Main Authors: Collins, Brittany C., Laakkonen, Eija K., Lowe, Dawn A.
Format: Article
Language:English
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Summary:Skeletal muscle weakness occurs with aging and in females this is compounded by the loss of estrogen with ovarian failure. Estrogen deficiency mediates decrements in muscle strength from both inadequate preservation of skeletal muscle mass and decrements in the quality of the remaining skeletal muscle. Processes and components of skeletal muscle that are affected by estrogens are beginning to be identified. This review focuses on mechanisms that contribute to the loss of muscle force generation when estrogen is low in females, and conversely the maintenance of strength by estrogen. Evidence is accumulating that estrogen deficiency induces apoptosis in skeletal muscle contributing to loss of mass and thus strength. Estrogen sensitive processes that affect quality, i.e., force generating capacity of muscle, include myosin phosphorylation and satellite cell function. Further detailing these mechanisms and identifying additional mechanisms that underlie estrogenic effects on skeletal muscle is important foundation for the design of therapeutic strategies to minimize skeletal muscle pathologies, such as sarcopenia and dynapenia. •Estrogen deficiency results in loss of muscle mass through apoptotic mechanisms.•Inconclusive evidence that loss of estrogen affects muscle protein turnover.•Dynapenia due to estrogen deficiency in females is related to myosin dysfunction.•Lack of estrogen impairs muscle regeneration ultimately impacting force generation.
ISSN:8756-3282
1873-2763
DOI:10.1016/j.bone.2019.03.033