Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/handle/10553/136685
Título: Remodeling p38 signaling in muscle controls locomotor activity via IL-15
Autores/as: Folgueira, Cintia
Herrera-Melle, Leticia
López, Juan Antonio
Galvan Alvarez,Victor 
Martín Rincón, Marcos 
Cuartero, María Isabel
García-Culebras, Alicia
Dumesic, Phillip A.
Rodríguez, Elena
Leiva-Vega, Luis
León, Marta
Porteiro, Begoña
Iglesias, Cristina
Torres, Jorge L.
Hernández-Cosido, Lourdes
Bonacasa, Clara
Marcos, Miguel
Moro, María Ángeles
Vázquez, Jesús
López Calbet, José Antonio 
Spiegelman, Bruce M.
Mora, Alfonso
Sabio, Guadalupe
Clasificación UNESCO: 241106 Fisiología del ejercicio
Palabras clave: Skeletal-Muscle
Insulin-Resistance
Interleukin-15
Exercise
Obesity, et al.
Fecha de publicación: 2024
Publicación seriada: Science Advances
Resumen: Skeletal muscle has gained recognition as an endocrine organ releasing myokines upon contraction during physical exercise. These myokines exert both local and pleiotropic health benefits, underscoring the crucial role of muscle function in countering obesity and contributing to the overall positive effects of exercise on health. Here, we found that exercise activates muscle p38γ, increasing locomotor activity through the secretion of interleukin-15 (IL-15). IL-15 signals in the motor cortex, stimulating locomotor activity. This activation of muscle p38γ, leading to an increase locomotor activity, plays a crucial role in reducing the risk of diabetes and liver steatosis, unveiling a vital muscle-brain communication pathway with profound clinical implications. The correlation between p38γ activation in human muscle during acute exercise and increased blood IL-15 levels highlights the potential therapeutic relevance of this pathway in treating obesity and metabolic diseases. These findings provide valuable insights into the molecular basis of exercise-induced myokine responses promoting physical activity.
URI: https://accedacris.ulpgc.es/handle/10553/136685
ISSN: 2375-2548
DOI: 10.1126/sciadv.adn5993
Fuente: Science advances[EISSN 2375-2548],v. 10 (33), (Agosto 2024)
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