Nature communications · 2023
Myonectin protects against skeletal muscle dysfunction in male mice through activation of AMPK/PGC1α pathway.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Ozaki Yuta, Ohashi Koji, Otaka Naoya, Kawanishi Hiroshi, Takikawa Tomonobu, Fang Lixin, Takahara Kunihiko, Tatsumi Minako, Ishihama Sohta, Takefuji Mikito, Kato Katsuhiro, Shimizu Yuuki, Bando Yasuko K, Inoue Aiko, Kuzuya Masafumi, Miura Shinji, Murohara Toyoaki, Ouchi Noriyuki
Аннотация
To maintain and restore skeletal muscle mass and function is essential for healthy aging. We have found that myonectin acts as a cardioprotective myokine. Here, we investigate the effect of myonectin on skeletal muscle atrophy in various male mouse models of muscle dysfunction. Disruption of myonectin exacerbates skeletal muscle atrophy in age-associated, sciatic denervation-induced or dexamethasone (DEX)-induced muscle atrophy models. Myonectin deficiency also contributes to exacerbated mitochondrial dysfunction and reduces expression of mitochondrial biogenesis-associated genes including PGC1α in denervated muscle. Myonectin supplementation attenuates denervation-induced muscle atrophy via activation of AMPK. Myonectin also reverses DEX-induced atrophy of cultured myotubes through the AMPK/PGC1α signaling. Furthermore, myonectin treatment suppresses muscle atrophy in senescence-accelerated mouse prone (SAMP) 8 mouse model of accelerated aging or mdx mouse model of Duchenne muscular dystrophy. These data indicate that myonectin can ameliorate skeletal muscle dysfunction through AMPK/PGC1α-dependent mechanisms, suggesting that myonectin could represent a therapeutic target of muscle atrophy.