Literature DB >> 23802635

The influence of skeletal muscle on systemic aging and lifespan.

Fabio Demontis1, Rosanna Piccirillo, Alfred L Goldberg, Norbert Perrimon.   

Abstract

Epidemiological studies in humans suggest that skeletal muscle aging is a risk factor for the development of several age-related diseases such as metabolic syndrome, cancer, Alzheimer's and Parkinson's disease. Here, we review recent studies in mammals and Drosophila highlighting how nutrient- and stress-sensing in skeletal muscle can influence lifespan and overall aging of the organism. In addition to exercise and indirect effects of muscle metabolism, growing evidence suggests that muscle-derived growth factors and cytokines, known as myokines, modulate systemic physiology. Myokines may influence the progression of age-related diseases and contribute to the intertissue communication that underlies systemic aging.
© 2013 the Anatomical Society and John Wiley & Sons Ltd.

Entities:  

Keywords:  exercise; intertissue communication during aging; myokine signaling; skeletal muscle aging; systemic aging

Mesh:

Substances:

Year:  2013        PMID: 23802635      PMCID: PMC3838468          DOI: 10.1111/acel.12126

Source DB:  PubMed          Journal:  Aging Cell        ISSN: 1474-9718            Impact factor:   9.304


  111 in total

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4.  A critical role of SNF1A/dAMPKalpha (Drosophila AMP-activated protein kinase alpha) in muscle on longevity and stress resistance in Drosophila melanogaster.

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5.  FOXO/4E-BP signaling in Drosophila muscles regulates organism-wide proteostasis during aging.

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8.  A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis.

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  74 in total

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Review 5.  Exercise capacity, physical activity, and morbidity.

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Review 6.  Control of Germline Stem Cell Lineages by Diet and Physiology.

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7.  Lisinopril Preserves Physical Resilience and Extends Life Span in a Genotype-Specific Manner in Drosophila melanogaster.

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Review 9.  Emerging molecular mediators and targets for age-related skeletal muscle atrophy.

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