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Science ; 371(6528)2021 01 29.
Artigo em Inglês | MEDLINE | ID: mdl-33303683

RESUMO

Treatments are lacking for sarcopenia, a debilitating age-related skeletal muscle wasting syndrome. We identifed increased amounts of 15-hydroxyprostaglandin dehydrogenase (15-PGDH), the prostaglandin E2 (PGE2)-degrading enzyme, as a hallmark of aged tissues, including skeletal muscle. The consequent reduction in PGE2 signaling contributed to muscle atrophy in aged mice and results from 15-PGDH-expressing myofibers and interstitial cells, such as macrophages, within muscle. Overexpression of 15-PGDH in young muscles induced atrophy. Inhibition of 15-PGDH, by targeted genetic depletion or a small-molecule inhibitor, increased aged muscle mass, strength, and exercise performance. These benefits arise from a physiological increase in PGE2 concentrations, which augmented mitochondrial function and autophagy and decreased transforming growth factor-ß signaling and activity of ubiquitin-proteasome pathways. Thus, PGE2 signaling ameliorates muscle atrophy and rejuvenates muscle function, and 15-PGDH may be a suitable therapeutic target for countering sarcopenia.


Assuntos
Envelhecimento/metabolismo , Dinoprostona/metabolismo , Hidroxiprostaglandina Desidrogenases/fisiologia , Músculo Esquelético/patologia , Rejuvenescimento , Sarcopenia/enzimologia , Animais , Morte Celular Autofágica/genética , Morte Celular Autofágica/fisiologia , Hidroxiprostaglandina Desidrogenases/antagonistas & inibidores , Hidroxiprostaglandina Desidrogenases/genética , Macrófagos/enzimologia , Camundongos , Camundongos Endogâmicos C57BL , Mitocôndrias Musculares/ultraestrutura , Força Muscular/genética , Força Muscular/fisiologia , Músculo Esquelético/enzimologia , Miofibrilas/enzimologia , Sarcopenia/genética
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