Aguirre Francisco, Valero-Breton Mayalen, Cabrera Daniel, Peñailillo Luis, Otero María Carolina, Fredes Claudia, Cabello-Verrugio Claudio
Center for Research on Pandemic Resilience, Faculty of Life Sciences and Institute of Public Health, Universidad Andres Bello, Santiago, Chile; Laboratory of Muscle Pathology, Fragility and Aging, Department of Biological Sciences, Faculty of Life Sciences, Universidad Andres Bello, Santiago, Chile; Millennium Institute on Immunology and Immunotherapy, Faculty of Life Sciences, Universidad Andres Bello, Santiago.
Center for Biomedical Research and Innovation (CiiB), Faculty of Medicine, Universidad de los Andes, Santiago, Chile; Facultad de Ciencias de la Salud, Escuela de Kinesiología, Universidad Bernardo O Higgins, Santiago.
Eur J Transl Myol. 2025 Jul 23. doi: 10.4081/ejtm.2025.13365.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a condition characterized by altered liver function due to fatty accumulation, which can lead to liver inflammation and, in advanced stages, liver carcinoma. MASLD is closely linked to several metabolic alterations, such as obesity and insulin resistance, which directly affect skeletal muscles and contribute to the development of sarcopenia. Sarcopenia is the loss of muscle mass and strength, leading to decreased physical performance in severe stages. Skeletal muscles secrete molecules known as myokines under various conditions, such as exercise or diseases like MASLD. These myokines modulate communication between the skeletal muscle and other tissues. These myokines regulate muscle mass and, in pathological conditions, contribute to the development of sarcopenia. Emerging evidence highlights the crucial role of myokines in regulating skeletal muscle metabolism and function in MASLD. Myokines influence muscle metabolism, inflammation, and insulin sensitivity, offering potential therapeutic targets for managing muscle atrophy and sarcopenia in the context of MASLD. Understanding the interaction between myokines and skeletal muscle may lead to novel interventions to mitigate MASLD progression and sarcopenia. This review examines the mechanisms by which myokines regulate skeletal muscle metabolism and function in the context of MASLD.
代谢功能障碍相关脂肪性肝病(MASLD)是一种由于脂肪堆积导致肝功能改变的病症,可引发肝脏炎症,在疾病晚期还可导致肝癌。MASLD与多种代谢改变密切相关,如肥胖和胰岛素抵抗,这些改变直接影响骨骼肌并促使肌肉减少症的发展。肌肉减少症是肌肉质量和力量的丧失,在严重阶段会导致身体机能下降。在各种情况下,如运动或患有MASLD等疾病时,骨骼肌会分泌一种称为肌动蛋白的分子。这些肌动蛋白调节骨骼肌与其他组织之间的通讯。这些肌动蛋白调节肌肉质量,在病理状态下,会促使肌肉减少症的发展。新出现的证据突出了肌动蛋白在调节MASLD中骨骼肌代谢和功能方面的关键作用。肌动蛋白影响肌肉代谢、炎症和胰岛素敏感性,为在MASLD背景下管理肌肉萎缩和肌肉减少症提供了潜在的治疗靶点。了解肌动蛋白与骨骼肌之间的相互作用可能会带来新的干预措施,以减轻MASLD的进展和肌肉减少症。本综述探讨了在MASLD背景下肌动蛋白调节骨骼肌代谢和功能的机制。