骨骼肌
内科学
内分泌学
过氧化物酶体增殖物激活受体
受体
肌肉萎缩
萎缩
化学
生物
分子生物学
医学
作者
Hiroshi Kumagai,Su‐Jeong Kim,Brendan Miller,Toshiharu Natsume,Junxiang Wan,Michi Emma Kumagai,Ricardo Ramírez,Shin Hyung Lee,Ayaka Sato,Hemal H. Mehta,Kelvin Yen,Pinchas Cohen
出处
期刊:American Journal of Physiology-endocrinology and Metabolism
[American Physiological Society]
日期:2024-01-03
卷期号:326 (3): E207-E214
被引量:2
标识
DOI:10.1152/ajpendo.00285.2023
摘要
MOTS-c, a mitochondrial microprotein, attenuates immobilization-induced skeletal muscle atrophy. MOTS-c treatment improves systemic inflammation and skeletal muscle AKT/FOXOs signaling pathways. Furthermore, unbiased RNA sequencing and subsequent assays revealed that MOTS-c prevents lipid infiltration in skeletal muscle. Since lipid accumulation is one of the common pathologies among other skeletal muscle atrophies induced by aging, obesity, cancer cachexia, and denervation, MOTS-c treatment could be effective in other muscle atrophy models as well.
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