Matches in SemOpenAlex for { <https://semopenalex.org/work/W2774229853> ?p ?o ?g. }
- W2774229853 endingPage "181" @default.
- W2774229853 startingPage "172" @default.
- W2774229853 abstract "Abstract Background Electrical stimulation is often used to treat weakness in people with spinal cord injury (SCI); however its efficacy for increasing strength and trophism is weak, and the mechanisms underlying the therapeutic benefits are unknown. Objective The purpose of this study was to analyze the effects of neuromuscular electrical stimulation (NMES) on muscle function, trophism, and the Akt pathway signaling involved in muscular plasticity after incomplete SCI in rats. Design This was an experimental study. Methods Twenty-one adult female Wistar rats were divided into sham, SCI, and SCI plus NMES groups. In injured animals, SCI hemisection was induced by a surgical procedure at the C5-C7 level. The 5-week NMES protocol consisted of biceps brachii muscle stimulation 5 times per week, initiated 48 h after injury. Forepaw function and strength, biceps muscle trophism, and the expression of phosphorylated Akt, p70S6K, and GSK-3ß cellular anabolic pathway markers in stimulated muscle tissue were assessed. Results There was an increase in bicep muscle strength in the NMES group compared with the untreated SCI group, from postoperative day 21 until the end of the evaluation period. Also, there was an increase in muscle trophism in the NMES group compared with the SCI group. Forelimb function gradually recovered in both the SCI group and the NMES group, with no differences between them. Regarding muscle protein expression, the NMES group had higher values for phospho-Akt, phospho-p70S6K, and phospho-GSK-3ß than did the SCI group. Limitations The experimental findings were limited to an animal model of incomplete SCI and may not be fully generalizable to humans. Conclusions Early cyclical NMES therapy was shown to increase muscle strength and induce hypertrophy after incomplete SCI in a rat model, probably by increasing phospho-Akt, phospho-p70S6K, and phospho-GSK-3ß signaling protein synthesis." @default.
- W2774229853 created "2017-12-22" @default.
- W2774229853 creator A5005085815 @default.
- W2774229853 creator A5009990459 @default.
- W2774229853 creator A5033329844 @default.
- W2774229853 creator A5034832381 @default.
- W2774229853 creator A5069326166 @default.
- W2774229853 creator A5073441920 @default.
- W2774229853 date "2017-12-12" @default.
- W2774229853 modified "2023-10-03" @default.
- W2774229853 title "Early Cyclical Neuromuscular Electrical Stimulation Improves Strength and Trophism by Akt Pathway Signaling in Partially Paralyzed Biceps Muscle After Spinal Cord Injury in Rats" @default.
- W2774229853 cites W1528110819 @default.
- W2774229853 cites W1733902486 @default.
- W2774229853 cites W1828575112 @default.
- W2774229853 cites W1970846603 @default.
- W2774229853 cites W1971809291 @default.
- W2774229853 cites W1992177813 @default.
- W2774229853 cites W1993476327 @default.
- W2774229853 cites W1995949259 @default.
- W2774229853 cites W2001868505 @default.
- W2774229853 cites W2014924738 @default.
- W2774229853 cites W2025085605 @default.
- W2774229853 cites W2039716494 @default.
- W2774229853 cites W2067908390 @default.
- W2774229853 cites W2070437133 @default.
- W2774229853 cites W2073720580 @default.
- W2774229853 cites W2080380613 @default.
- W2774229853 cites W2082813420 @default.
- W2774229853 cites W2102438984 @default.
- W2774229853 cites W2106581113 @default.
- W2774229853 cites W2118353927 @default.
- W2774229853 cites W2145305562 @default.
- W2774229853 cites W2160030455 @default.
- W2774229853 cites W2218982377 @default.
- W2774229853 cites W2325540833 @default.
- W2774229853 cites W2331396408 @default.
- W2774229853 cites W2353665364 @default.
- W2774229853 cites W2461734239 @default.
- W2774229853 cites W2626887228 @default.
- W2774229853 cites W303407348 @default.
- W2774229853 cites W4293247451 @default.
- W2774229853 cites W817820422 @default.
- W2774229853 doi "https://doi.org/10.1093/ptj/pzx116" @default.
- W2774229853 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29240948" @default.
- W2774229853 hasPublicationYear "2017" @default.
- W2774229853 type Work @default.
- W2774229853 sameAs 2774229853 @default.
- W2774229853 citedByCount "9" @default.
- W2774229853 countsByYear W27742298532018 @default.
- W2774229853 countsByYear W27742298532019 @default.
- W2774229853 countsByYear W27742298532022 @default.
- W2774229853 countsByYear W27742298532023 @default.
- W2774229853 crossrefType "journal-article" @default.
- W2774229853 hasAuthorship W2774229853A5005085815 @default.
- W2774229853 hasAuthorship W2774229853A5009990459 @default.
- W2774229853 hasAuthorship W2774229853A5033329844 @default.
- W2774229853 hasAuthorship W2774229853A5034832381 @default.
- W2774229853 hasAuthorship W2774229853A5069326166 @default.
- W2774229853 hasAuthorship W2774229853A5073441920 @default.
- W2774229853 hasBestOaLocation W27742298531 @default.
- W2774229853 hasConcept C1008401 @default.
- W2774229853 hasConcept C105702510 @default.
- W2774229853 hasConcept C118552586 @default.
- W2774229853 hasConcept C126322002 @default.
- W2774229853 hasConcept C24998067 @default.
- W2774229853 hasConcept C2778334475 @default.
- W2774229853 hasConcept C2778646069 @default.
- W2774229853 hasConcept C2780775167 @default.
- W2774229853 hasConcept C2781425419 @default.
- W2774229853 hasConcept C42219234 @default.
- W2774229853 hasConcept C71924100 @default.
- W2774229853 hasConcept C99508421 @default.
- W2774229853 hasConceptScore W2774229853C1008401 @default.
- W2774229853 hasConceptScore W2774229853C105702510 @default.
- W2774229853 hasConceptScore W2774229853C118552586 @default.
- W2774229853 hasConceptScore W2774229853C126322002 @default.
- W2774229853 hasConceptScore W2774229853C24998067 @default.
- W2774229853 hasConceptScore W2774229853C2778334475 @default.
- W2774229853 hasConceptScore W2774229853C2778646069 @default.
- W2774229853 hasConceptScore W2774229853C2780775167 @default.
- W2774229853 hasConceptScore W2774229853C2781425419 @default.
- W2774229853 hasConceptScore W2774229853C42219234 @default.
- W2774229853 hasConceptScore W2774229853C71924100 @default.
- W2774229853 hasConceptScore W2774229853C99508421 @default.
- W2774229853 hasIssue "3" @default.
- W2774229853 hasLocation W27742298531 @default.
- W2774229853 hasLocation W27742298532 @default.
- W2774229853 hasOpenAccess W2774229853 @default.
- W2774229853 hasPrimaryLocation W27742298531 @default.
- W2774229853 hasRelatedWork W1572510040 @default.
- W2774229853 hasRelatedWork W1968324212 @default.
- W2774229853 hasRelatedWork W1973259926 @default.
- W2774229853 hasRelatedWork W2045360664 @default.
- W2774229853 hasRelatedWork W2806854514 @default.
- W2774229853 hasRelatedWork W2990323769 @default.
- W2774229853 hasRelatedWork W3002155050 @default.
- W2774229853 hasRelatedWork W3192634125 @default.
- W2774229853 hasRelatedWork W4294647463 @default.