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dc.creatorLhamyani, Saides
dc.creatorGentile, Adriana Marieles
dc.creatorMengual Mesa, Maríaes
dc.creatorGrueso Molina, Elia Maríaes
dc.creatorGiráldez Pérez, Rosa Maríaes
dc.creatorFernandez Garcia, José Carloses
dc.creatorVega Rioja, Antonioes
dc.creatorClemente Postigo, Mercedeses
dc.creatorEl Bekay, Rajaaes
dc.date.accessioned2024-01-11T12:39:18Z
dc.date.available2024-01-11T12:39:18Z
dc.date.issued2024-02
dc.identifier.citationLhamyani, S., Gentile, A.M., Mengual Mesa, M., Grueso Molina, E.M., Giráldez Pérez, R.M., Fernandez Garcia, J.C.,...,El Bekay, R. (2024). Au@16-pH-16/miR-21 mimic nanosystem: An efficient treatment for obesity through browning and thermogenesis induction. Biomedicine & Pharmacotherapy, 171, 116104. https://doi.org/10.1016/j.biopha.2023.116104.
dc.identifier.issn0753-3322es
dc.identifier.issn1950-6007es
dc.identifier.urihttps://hdl.handle.net/11441/153240
dc.description.abstractDespite the abundance of registered clinical trials worldwide, the availability of effective drugs for obesity treatment is limited due to their associated side effects. Thus, there is growing interest in therapies that stimulate energy expenditure in white adipose tissue. Recently, we demonstrated that the delivery of a miR-21 mimic using JetPEI effectively inhibits weight gain in an obese mouse model by promoting metabolism, browning, and thermogenesis, suggesting the potential of miR-21 mimic as a treatment for obesity. Despite these promising results, the implementation of more advanced delivery system techniques for miR-21 mimic would greatly enhance the advancement of safe and efficient treatment approaches for individuals with obesity in the future. Our objective is to explore whether a new delivery system based on gold nanoparticles and Gemini surfactants (Au@16-ph-16) can replicate the favorable effects of the miR-21 mimic on weight gain, browning, and thermogenesis. We found that dosages as low as 0.2 μg miR-21 mimic /animal significantly inhibited weight gain and induced browning and thermogenic parameters. This was evidenced by the upregulation of specific genes and proteins associated with these processes, as well as the biogenesis of beige adipocytes and mitochondria. Significant increases in miR-21 levels were observed in adipose tissue but not in other tissue types. Our data indicates that Au@16-ph-16 could serve as an effective delivery system for miRNA mimics, suggesting its potential suitability for the development of future clinical treatments against obesity.es
dc.description.sponsorshipInstituto de Salud Carlos III (ISCIII) PI21/01924, PI18/00785es
dc.description.sponsorshipEuropean Union (UE) PI21/01924, PI18/00785es
dc.description.sponsorshipEuropean Commission (EC). Fondo Europeo de Desarrollo Regional (FEDER) PI20-01274es
dc.description.sponsorshipUniversidad de Sevilla 2021/00001297es
dc.description.sponsorshipJunta de Andalucía PI20-01274, PI-0235-2021, DOC-01138, RC-0006-2020, C-0060-2018, PI-0092–2017es
dc.description.sponsorshipUniversidad de Málaga RC-0001-2021es
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO). España SAF2014-60649-JINes
dc.formatapplication/pdfes
dc.format.extent11 p.es
dc.language.isoenges
dc.publisherElsevieres
dc.relation.ispartofBiomedicine & Pharmacotherapy, 171, 116104.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMiRNAes
dc.subjectGold Nanoparticleses
dc.subjectGemini surfactantes
dc.subjectObesityes
dc.subjectAdipose tissuees
dc.subjectBrowninges
dc.subjectThermogenesises
dc.titleAu@16-pH-16/miR-21 mimic nanosystem: An efficient treatment for obesity through browning and thermogenesis inductiones
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Química Físicaes
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicinaes
dc.relation.projectIDPI21/01924es
dc.relation.projectIDPI18/00785es
dc.relation.projectIDPI20-01274es
dc.relation.projectIDPI-0235-2021es
dc.relation.projectIDDOC-01138es
dc.relation.projectIDRC-0006-2020es
dc.relation.projectIDC-0060-2018es
dc.relation.projectID2021/00001297es
dc.relation.projectIDPI-0092–2017es
dc.relation.projectIDRC-0001-2021es
dc.relation.projectIDSAF2014-60649-JINes
dc.relation.publisherversionhttps://doi.org/10.1016/j.biopha.2023.116104es
dc.identifier.doi10.1016/j.biopha.2023.116104es
dc.journaltitleBiomedicine & Pharmacotherapyes
dc.publication.volumen171es
dc.publication.initialPage116104es
dc.contributor.funderInstituto de Salud Carlos III (ISCIII)es
dc.contributor.funderEuropean Union (UE)es
dc.contributor.funderJunta de Andalucíaes
dc.contributor.funderEuropean Commission (EC). Fondo Europeo de Desarrollo Regional (FEDER)es
dc.contributor.funderUniversidad de Sevillaes
dc.contributor.funderUniversidad de Málagaes
dc.contributor.funderMinisterio de Economía y Competitividad (MINECO). Españaes

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