Journal
CURRENT PHARMACEUTICAL DESIGN
Volume 27, Issue 27, Pages 3012-3019Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1381612824666210316102413
Keywords
Muscle atrophy; physical inactivity; ubiquitin-proteasome system; corticosteroids; aging; stimulus
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Muscle wasting can be categorized into three main subgroups: physiologic, pathologic, and neurogenic atrophy, each with distinct causes and mechanisms. While some pathways have been elucidated, additional research is needed to properly classify and identify muscle atrophy.
It is well known that muscles can waste away (atrophy) due to a lack of physical activity. Muscle wasting commonly presents with reduced muscle strength and an impaired ability to perform daily tasks. Sever-al studies have attempted to categorize muscle atrophy into three main subgroups: physiologic, pathologic, and neurogenic atrophy. Physiologic atrophy is caused by the general underuse of skeletal muscle (e.g., bedridden). Pathologic atrophy is characterized as the loss of stimulus to a specific region (e.g., aging). Neurogenic atrophy results from damage to the nerve innervating a muscle (e.g., SMA, GBS). Mechanisms have been elucidated for many of these pathways (e.g., ubiquitin-proteasome system, NF-Kappa B, etc.). However, many causes of muscle at-rophy (e.g., burns, arthritis, etc.) operate through unelucidated signaling cascades. Therefore, this review high-lights the underlying mechanisms of each subtype of muscle atrophy while emphasizing the need for additional research in properly classifying and identifying muscle atrophy.
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