Publication: Implications of maraviroc and/or rapamycin in a mouse model of fragility.
dc.contributor.author | Pérez-Martínez, Laura | |
dc.contributor.author | Romero, Lourdes | |
dc.contributor.author | Muñoz-Galván, Sandra | |
dc.contributor.author | Verdugo-Sivianes, Eva M | |
dc.contributor.author | Rubio-Mediavilla, Susana | |
dc.contributor.author | Oteo, José A | |
dc.contributor.author | Carnero, Amancio | |
dc.contributor.author | Blanco, José-Ramón | |
dc.date.accessioned | 2023-02-08T14:48:03Z | |
dc.date.available | 2023-02-08T14:48:03Z | |
dc.date.issued | 2020-04-30 | |
dc.description.abstract | As age increases, the risk of developing fragility also increases. Improving the knowledge of frailty could contribute to maintaining the functional ability of elderly people. Interleukin (IL)-10 homozygous knockout mice (IL-10tm/tm [IL10KO]) constitute an excellent tool for the study of frailty. Because patients with frailty demonstrate an overexpression of CCR5, rapamycin (RAPA) and/or maraviroc (MVC), two molecules able to decrease CCR5 expression, were evaluated. Muscle myostatin was reduced in all the therapeutic groups but the MVC group (p MVC and RAPA show a protective role in some factors involved in frailty. More studies are needed to prove their clinical applications. Eighty male homozygous IL10KOs were randomly assigned to one of 4 groups (n= 20): i) IL10KO group (IL10KO); ii) IL10KO receiving MVC in drinking water (MVC group), iii) IL10KO receiving RAPA in drinking water (RAPA group), and finally, iv) MVC-RAPA group that received MVC and RAPA in drinking water. Blood and muscle samples were analysed. Survival analysis, frailty index calculation, and functional assessment were also performed. | |
dc.identifier.doi | 10.18632/aging.103167 | |
dc.identifier.essn | 1945-4589 | |
dc.identifier.pmc | PMC7244075 | |
dc.identifier.pmid | 32353830 | |
dc.identifier.pubmedURL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244075/pdf | |
dc.identifier.unpaywallURL | https://doi.org/10.18632/aging.103167 | |
dc.identifier.uri | http://hdl.handle.net/10668/15471 | |
dc.issue.number | 9 | |
dc.journal.title | Aging | |
dc.journal.titleabbreviation | Aging (Albany NY) | |
dc.language.iso | en | |
dc.organization | Instituto de Biomedicina de Sevilla-IBIS | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.page.number | 8565-8582 | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.rights | Attribution 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | CCR5 antagonist | |
dc.subject | frailty | |
dc.subject | myostatin | |
dc.subject | rapamycin | |
dc.subject.mesh | Aging | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Cytokines | |
dc.subject.mesh | Disease Models, Animal | |
dc.subject.mesh | Frailty | |
dc.subject.mesh | Interleukin-10 | |
dc.subject.mesh | Male | |
dc.subject.mesh | Maraviroc | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Mice, Knockout | |
dc.subject.mesh | Muscle, Skeletal | |
dc.subject.mesh | Random Allocation | |
dc.subject.mesh | Receptors, Chemokine | |
dc.subject.mesh | Sirolimus | |
dc.subject.mesh | Survival Rate | |
dc.title | Implications of maraviroc and/or rapamycin in a mouse model of fragility. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 12 | |
dspace.entity.type | Publication |
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