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dc.contributor.authorMatías-Valiente, Lidia
dc.contributor.authorSánchez Fernández, Cristina 
dc.contributor.authorRodríguez-Outeiriño, Lara
dc.contributor.authorRamos, María C.
dc.contributor.authorDíaz, Caridad
dc.contributor.authorCrespo, Gloria
dc.contributor.authorGonzález-Menéndez, Víctor
dc.contributor.authorGenilloud, Olga
dc.contributor.authorReyes, Fernando
dc.contributor.authorMontolio, Marisol
dc.contributor.authorHernández-Torres, Francisco
dc.contributor.authorAranega, Amelia Eva
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-01-08T18:55:11Z
dc.date.available2025-01-08T18:55:11Z
dc.date.issued2024
dc.identifier.issn0753-3322
dc.identifier.issn1950-6007
dc.identifier.urihttps://hdl.handle.net/10902/34901
dc.description.abstractDuchenne muscular dystrophy (DMD) is a devastating degenerative disease of skeletal muscles caused by loss of dystrophin, a key protein that maintains muscle integrity, which leads to progressive muscle degeneration aggravated by chronic inflammation, muscle stem cells' (MuSCs) reduced regenerative capacity and replacement of muscle with fibroadipose tissue. Previous research has shown that pharmacological GSK-3β inhibition favors myogenic differentiation and plays an important role in modulating inflammatory processes. Isolecanoric acid (ILA) is a natural product isolated from a fungal culture displaying GSK-3β inhibitory properties. The present study aimed to investigate the proregenerative and anti-inflammatory properties of this natural compound in the DMD context. Our results showed that ILA markedly promotes myogenic differentiation of myoblasts by increasing Beta-Catenin signaling and boosting the myogenic potential of mouse and human stem cells. One important finding was that the GSK-3β/β-Catenin pathway is altered in dystrophic mice muscle and ILA enhances the myofiber formation of dystrophic MuSCs. Treatment with this natural compound improves muscle regeneration of dystrophic mice by, in turn, improving functional performance. Moreover, ILA ameliorates the inflammatory response in both muscle explants and the macrophages isolated from dystrophic mice to, thus, mitigate fibrosis after muscle damage. Overall, we show that ILA modulates both inflammation and muscle regeneration to, thus, contribute to improve the dystrophic phenotype.es_ES
dc.description.sponsorshipFunding sources: This work was supported by the Duchenne Parent Project, Spain Foundation (grant number DUCHENNE_2018/001). Ministerio de Ciencia e Innovación, Gobierno de España (grant number PID2022–138163OB-C31). Consejeria de Universidad, Investigacion e Innovacion, Junta de Andalucia (grant number ProyExcel_00513). Acknowledgement: This work was partially supported by grants DUCHENNE_2018/001 (Duchenne Parent Project, Spain Foundation), PID2022–138163OB-C31 (Ministerio de Ciencia e Innovación, Gobierno de España) and ProyExcel_00513 (Consejeria de Universidad, Investigacion e Innovacion, Junta de Andalucia).es_ES
dc.format.extent16 p.es_ES
dc.language.isoenges_ES
dc.publisherEditions Scientifiques Elsevieres_ES
dc.rights© 2023 The Authors. Published by Elsevier Masson SAS. This is an open access article under the CC BY-NC-ND license.es_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceBiomedicine & Pharmacotherapy, 2024, 170, 116056es_ES
dc.subject.otherDuchenne muscular dystrophyes_ES
dc.subject.otherMuscle stem cellses_ES
dc.subject.otherInflammatory responsees_ES
dc.subject.otherNatural productses_ES
dc.subject.otherIsolecanoric acides_ES
dc.titleEvaluation of pro-regenerative and anti-inflammatory effects of isolecanoric acid in the muscle: potential treatment of Duchenne Muscular Dystrophyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.biopha.2023.116056es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.biopha.2023.116056
dc.type.versionpublishedVersiones_ES


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© 2023 The Authors. Published by Elsevier Masson SAS. This is an open access article under the CC BY-NC-ND license.Excepto si se señala otra cosa, la licencia del ítem se describe como © 2023 The Authors. Published by Elsevier Masson SAS. This is an open access article under the CC BY-NC-ND license.