Moreno Ruperez, ÁlvaroPriego Cuadra, TeresaGonzález Nicolás González, María ÁngelesLópez-Calderón Barreda, AsunciónLázaro Fernández, AlbertoMartín Velasco, Ana Isabel2023-06-222023-06-222022-03-26Moreno Rupérez, Á., Priego Cuadra, T., González Nicolás González, M. Á. et al. «Role of Glucocorticoid Signaling and HDAC4 Activation in Diaphragm and Gastrocnemius Proteolytic Activity in Septic Rats». International Journal of Molecular Sciences, vol. 23, n.o 7, marzo de 2022, p. 3641. DOI.org (Crossref), https://doi.org/10.3390/ijms23073641.1422-006710.3390/ijms23073641https://hdl.handle.net/20.500.14352/72281Sepsis increases glucocorticoid and decreases IGF-1, leading to skeletal muscle wasting and cachexia. Muscle atrophy mainly takes place in locomotor muscles rather than in respiratory ones. Our study aimed to elucidate the mechanism responsible for this difference in muscle proteolysis, focusing on local inflammation and IGF-1 as well as on their glucocorticoid response and HDAC4-myogenin activation. Sepsis was induced in adult male rats by lipopolysaccharide (LPS) injection (10 mg/kg), and 24 h afterwards, rats were euthanized. LPS increased TNFα and IL-10 expression in both muscles studied, the diaphragm and gastrocnemius, whereas IL-6 and SOCS3 mRNA increased only in diaphragm. In comparison with gastrocnemius, diaphragm showed a lower increase in proteolytic marker expression (atrogin-1 and LC3b) and in LC3b protein lipidation after LPS administration. LPS increased the expression of glucocorticoid induced factors, KLF15 and REDD1, and decreased that of IGF-1 in gastrocnemius but not in the diaphragm. In addition, an increase in HDAC4 and myogenin expression was induced by LPS in gastrocnemius, but not in the diaphragm. In conclusion, the lower activation of both glucocorticoid signaling and HDAC4-myogenin pathways by sepsis can be one of the causes of lower sepsis-induced proteolysis in the diaphragm compared to gastrocnemius.engAtribución 3.0 Españahttps://creativecommons.org/licenses/by/3.0/es/journal articlehttps://doi.org/10.3390/ijms23073641https://www.mdpi.com/1422-0067/23/7/3641open access616-089.165SepsisInflammationMuscle wastingGlucocorticoids signalingHDAC4-myogeninIGF-1IGFBP3AtrogensAutophagyEnfermería, Fisioterapia y Podología