Matches in SemOpenAlex for { <https://semopenalex.org/work/W2967322172> ?p ?o ?g. }
- W2967322172 endingPage "110687" @default.
- W2967322172 startingPage "110687" @default.
- W2967322172 abstract "Aging is associated with reduced specific strength, defined as strength normalized to the cross-sectional area of a given muscle or muscle group. Dysregulated autophagy, impairing removal of dysfunctional proteins and organelles, is suggested as one of the underlying mechanisms. The aim of this study was to investigate levels of autophagic markers in skeletal muscle in groups known to differ in specific strength. Sixty-two volunteers were assigned to the following study groups: young, old non-frail, old pre-frail, and old frail individuals. Leg lean mass was assessed with dual-energy X-ray absorptiometry and quadriceps femoris muscle strength by isometric maximal voluntary contraction. The abundance of autophagic proteins within skeletal muscle cytosolic and membrane sub-fractions were determined by western blotting. In addition, the level of heat shock proteins and proteins involved in the regulation of protein synthesis were measured. The abundance of LC3-I was higher in old frail compared to young individuals. If the three elderly groups were pooled, the level of LC3-II was higher in old compared to young subjects. Pre-frail and frail elderly also displayed higher levels of certain heat shock proteins. No between-group differences were observed for p62, LC3-II/LC3-I ratio, or any of the anabolic signaling molecules. A negative correlation was observed between cytosolic LC3-I and specific strength. Higher levels of LC3-I in the frail elderly might represent attenuated autophagosome formation. However, higher LC3-II levels indicate an increased abundance of autophagosomes. These findings may therefore imply that both the process of autophagosome formation and autophagosome-lysosome fusion are affected in frail elderly. Higher levels of heat shock proteins might represent an auto-protective mechanism against increased levels of misfolded proteins, possibly due to inefficient degradation. In conclusion, the reduction in specific strength with aging and frailty may partly be caused by alterations in muscle protein quality control." @default.
- W2967322172 created "2019-08-22" @default.
- W2967322172 creator A5010767794 @default.
- W2967322172 creator A5013424976 @default.
- W2967322172 creator A5023139205 @default.
- W2967322172 creator A5023388480 @default.
- W2967322172 creator A5024556864 @default.
- W2967322172 creator A5029820784 @default.
- W2967322172 creator A5034491746 @default.
- W2967322172 creator A5035926886 @default.
- W2967322172 creator A5043230171 @default.
- W2967322172 creator A5083087105 @default.
- W2967322172 creator A5063789249 @default.
- W2967322172 date "2019-10-01" @default.
- W2967322172 modified "2023-09-25" @default.
- W2967322172 title "The impact of age and frailty on skeletal muscle autophagy markers and specific strength: A cross-sectional comparison" @default.
- W2967322172 cites W148671107 @default.
- W2967322172 cites W1838896829 @default.
- W2967322172 cites W1853625016 @default.
- W2967322172 cites W1874817816 @default.
- W2967322172 cites W1963521777 @default.
- W2967322172 cites W1966419450 @default.
- W2967322172 cites W1977767269 @default.
- W2967322172 cites W1979298497 @default.
- W2967322172 cites W1983802110 @default.
- W2967322172 cites W1986623178 @default.
- W2967322172 cites W1989482424 @default.
- W2967322172 cites W1991562722 @default.
- W2967322172 cites W1993476327 @default.
- W2967322172 cites W2002636911 @default.
- W2967322172 cites W2036787961 @default.
- W2967322172 cites W2039137539 @default.
- W2967322172 cites W2041198637 @default.
- W2967322172 cites W2050267353 @default.
- W2967322172 cites W2052991849 @default.
- W2967322172 cites W2054594032 @default.
- W2967322172 cites W2060792177 @default.
- W2967322172 cites W2065363098 @default.
- W2967322172 cites W2067636508 @default.
- W2967322172 cites W2087317993 @default.
- W2967322172 cites W2096657471 @default.
- W2967322172 cites W2101897425 @default.
- W2967322172 cites W2105439389 @default.
- W2967322172 cites W2119448420 @default.
- W2967322172 cites W2124679472 @default.
- W2967322172 cites W2134036439 @default.
- W2967322172 cites W2144142427 @default.
- W2967322172 cites W2150683917 @default.
- W2967322172 cites W2157509107 @default.
- W2967322172 cites W2159296038 @default.
- W2967322172 cites W2164059021 @default.
- W2967322172 cites W2164778558 @default.
- W2967322172 cites W2167033037 @default.
- W2967322172 cites W2167512318 @default.
- W2967322172 cites W2177646965 @default.
- W2967322172 cites W2184656706 @default.
- W2967322172 cites W2418360479 @default.
- W2967322172 cites W2518281858 @default.
- W2967322172 cites W2590970381 @default.
- W2967322172 cites W2617424984 @default.
- W2967322172 cites W2617788488 @default.
- W2967322172 cites W2676530931 @default.
- W2967322172 cites W2884054234 @default.
- W2967322172 cites W2931342787 @default.
- W2967322172 doi "https://doi.org/10.1016/j.exger.2019.110687" @default.
- W2967322172 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31404624" @default.
- W2967322172 hasPublicationYear "2019" @default.
- W2967322172 type Work @default.
- W2967322172 sameAs 2967322172 @default.
- W2967322172 citedByCount "20" @default.
- W2967322172 countsByYear W29673221722019 @default.
- W2967322172 countsByYear W29673221722020 @default.
- W2967322172 countsByYear W29673221722021 @default.
- W2967322172 countsByYear W29673221722022 @default.
- W2967322172 countsByYear W29673221722023 @default.
- W2967322172 crossrefType "journal-article" @default.
- W2967322172 hasAuthorship W2967322172A5010767794 @default.
- W2967322172 hasAuthorship W2967322172A5013424976 @default.
- W2967322172 hasAuthorship W2967322172A5023139205 @default.
- W2967322172 hasAuthorship W2967322172A5023388480 @default.
- W2967322172 hasAuthorship W2967322172A5024556864 @default.
- W2967322172 hasAuthorship W2967322172A5029820784 @default.
- W2967322172 hasAuthorship W2967322172A5034491746 @default.
- W2967322172 hasAuthorship W2967322172A5035926886 @default.
- W2967322172 hasAuthorship W2967322172A5043230171 @default.
- W2967322172 hasAuthorship W2967322172A5063789249 @default.
- W2967322172 hasAuthorship W2967322172A5083087105 @default.
- W2967322172 hasConcept C1008401 @default.
- W2967322172 hasConcept C103486182 @default.
- W2967322172 hasConcept C104317684 @default.
- W2967322172 hasConcept C126322002 @default.
- W2967322172 hasConcept C134018914 @default.
- W2967322172 hasConcept C190283241 @default.
- W2967322172 hasConcept C203522944 @default.
- W2967322172 hasConcept C205260736 @default.
- W2967322172 hasConcept C2776214593 @default.
- W2967322172 hasConcept C2779959927 @default.
- W2967322172 hasConcept C42407357 @default.