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Invited Review: Intracellular signaling in contracting skeletal muscle
Abstract
Physical exercise is a significant stimulus for the regulation of multiple metabolic and transcriptional processes in skeletal muscle. For example, exercise increases skeletal muscle glucose uptake, and, after exercise, there are increases in the rates of both glucose uptake and glycogen synthesis. A single bout of exercise can also induce transient changes in skeletal muscle gene transcription and can alter rates of protein metabolism, both of which may be mechanisms for chronic adaptations to repeated bouts of exercise. A central issue in exercise biology is to elucidate the underlying molecular signaling mechanisms that regulate these important metabolic and transcriptional events in skeletal muscle. In this review, we summarize research from the past several years that has demonstrated that physical exercise can regulate multiple intracellular signaling cascades in skeletal muscle. It is now well established that physical exercise or muscle contractile activity can activate three of the mitogen-activated protein kinase signaling pathways, including the extracellular signal-regulated kinase 1 and 2, the c-Jun NH 2-terminal kinase, and the p38. Exercise can also robustly increase activity of the AMP-activated protein kinase, as well as several additional molecules, including glycogen synthase kinase 3, Akt, and the p70 S6 kinase. A fundamental goal of signaling research is to determine the biological consequences of exercise-induced signaling through these molecules, and this review also provides an update of progress in this area.
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Self-citationInsulin-stimulated GLUT4 Translocation Is Mediated by a Divergent Intracellular Signaling Pathway
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Self-citationExercise diminishes the activity of acetyl-CoA carboxylase in human muscle.
Dean, D., Daugaard, J. R., Young, M. E., Saha, A. K., Vavvas, D. G., Asp, S., Kiens, B., Kim, K. H., Witters, L. A., Richter, E. A., et al. (2000) · Diabetes · doi:10.2337/diabetes.49.8.1295 · Cited by 127
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A Novel Role of Neuregulin in Skeletal Muscle
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Effect of AICAR Treatment on Glycogen Metabolism in Skeletal Muscle
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Self-citationjun N-terminal Kinase Mediates Activation of Skeletal Muscle Glycogen Synthase by Insulin in Vivo
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Self-citationEccentric exercise markedly increases c-Jun NH 2 -terminal kinase activity in human skeletal muscle
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Self-citationContractile Activity Stimulates the c-Jun NH2-terminal Kinase Pathway in Rat Skeletal Muscle
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Insulin Signaling After Exercise in Insulin Receptor Substrate-2-Deficient Mice
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7 Integrative Biology of Nitric Oxide and Exercise
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Metadata
- Authors
- Sakamoto, K., & Goodyear, L. J.
- Venue
- Journal of Applied Physiology
- Publisher
- American Physiological Society
- Published
- 2002-07-01
- Volume
- 93
- Issue
- 1
- Pages
- 369-383
- ISSN
- 0161-7567 (ISSN-L)
- 8750-7587
- 1522-1601
- OpenAlex
- W2157054897
- Cited by
- 264
- References
- 157
- FWCI
- 6.16
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.