The DOI matches its Crossref record; 211 of the 211 references it cites were found in a registry or an index.
Lipid metabolism in skeletal muscle: generation of adaptive and maladaptive intracellular signals for cellular function
Abstract
Fatty acids derived from adipose tissue lipolysis, intramyocellular triacylglycerol lipolysis, or de novo lipogenesis serve a variety of functions in skeletal muscle. The two major fates of fatty acids are mitochondrial oxidation to provide energy for the myocyte and storage within a variety of lipids, where they are stored primarily in discrete lipid droplets or serve as important structural components of membranes. In this review, we provide a brief overview of skeletal muscle fatty acid metabolism and highlight recent notable advances in the field. We then 1) discuss how lipids are stored in and mobilized from various subcellular locations to provide adaptive or maladaptive signals in the myocyte and 2) outline how lipid metabolites or metabolic byproducts derived from the actions of triacylglycerol metabolism or β-oxidation act as positive and negative regulators of insulin action. We have placed an emphasis on recent developments in the lipid biology field with respect to understanding skeletal muscle physiology and discuss unanswered questions and technical limitations for assessing lipid signaling in skeletal muscle.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“an accumulation of these fatty acids and ceramides and diacylglycerol in the cytosolic compartment are linked to insulin resistance via an inhibition of the insulin signaling cascade (36,37).”
From Simvastatin Effects on Skeletal Muscle (2013) · cites this paper as [37]
Citations
Cites
Items 201–211 of 211
Effects of sphingosine 1-phosphate on excitation–contraction coupling in mammalian skeletal muscle
Bencini, C., Squecco, R., Piperio, C., Formigli, L., Meacci, E., Nosi, D., Tiribilli, B., Vassalli, M., Quercioli, F., Bruni, P., et al. (2003) · Journal of Muscle Research and Cell Motility · doi:10.1023/b:jure.0000009898.02325.58 · Cited by 29
Contribution of intermuscular fat to lipogenesis from dietary glucose carbon in mice
Kannan, R. R., Palmquist, D. L., & Baker, N. (1976) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(76)90142-9 · Cited by 28
Harriman, D. G. F., & Reed, R. (1972) · The Journal of Pathology · doi:10.1002/path.1711060102 · Cited by 26
Formigli, L., Meacci, E., Vassalli, M., Nosi, D., Quercioli, F., Tiribilli, B., Tani, A., Squecco, R., Francini, F., Bruni, P., et al. (2003) · Journal of Cellular Physiology · doi:10.1002/jcp.10366 · Cited by 25
Thrush, A. B., Harasim‐Symbor, E., Chabowski, A., Gulli, R. A., Stefanyk, L. E., & Dyck, D. J. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00091.2010 · Cited by 25
Cazzolli, R., Mitchell, T. W., Burchfield, J. G., Pedersen, D. J., Turner, N. A., Biden, T. J., & Schmitz‐Peiffer, C. (2007) · Diabetologia · doi:10.1007/s00125-007-0709-x · Cited by 25
Sphingosine 1-phosphate evokes calcium signals in C2C12 myoblasts via Edg3 and Edg5 receptors
Meacci, E., Cencetti, F., Formigli, L., et al. (2002) · Biochemical Journal · doi:10.1042/bj3620349 · Cited by 25
Kanshin, E., Wang, S., ASHMARINA, L. I., Fedjaev, M., Nifant'ev, I. E., Mitchell, G. A., & Pshezhetsky, A. V. (2009) · PROTEOMICS · doi:10.1002/pmic.200800861 · Cited by 24
Stratford, S. (2004) · Medical Entomology and Zoology · Cited by 17
Insulin increases a biochemically distinct pool of diacylglycerol in the rat soleus muscle
Chen, K. S., Heydrick, S. J., Brown, M. L., Friel, J., & Ruderman, N. B. (1994) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1994.266.3.e479 · Cited by 17
Lipid partitioning and insulin sensitivity: Lessons learnt from genetic models
Hoy, A. J., & Watt, M. J. (2009) · Cited by 4
Flagged first, then by citations
Research works printed but not linked: 4
- Gangoiti P, Biochimie
- 10.1210/jcem.86.12.8075 · DOI · Paper page
- Hoy AJ, 2009, APJOE, 1, 35
- Szendroedi J, Nat Rev Endocrinol
Cited by
Sorted by citations
Single-Cell Transcriptome Atlas of Murine Endothelial Cells
Kalucka, J. M., de Rooij, L. P. M. H., Goveia, J., Rohlenová, K., Dumas, S. J., Meta, E., Conchinha, N. V., Taverna, F., Teuwen, L.-A. M. N., Veys, K., et al. (2020) · Cell · doi:10.1016/j.cell.2020.01.015 · Cited by 1,356
Sugar consumption, metabolic disease and obesity: The state of the controversy
Stanhope, K. L. (2016) · Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408363.2015.1084990 · Cited by 739
Lipids, lysosomes, and autophagy
Jaishy, B. P., & Abel, E. D. (2016) · Journal of Lipid Research · doi:10.1194/jlr.r067520 · Cited by 239
Fatty acid metabolism, energy expenditure and insulin resistance in muscle
Turner, N. A., Cooney, G. J., Kraegen, E. W., & Bruce, C. R. (2013) · Journal of Endocrinology · doi:10.1530/joe-13-0397 · Cited by 206
Lipotoxicity in Kidney, Heart, and Skeletal Muscle Dysfunction
Nishi, H., Higashihara, T., & Inagi, R. (2019) · Nutrients · doi:10.3390/nu11071664 · Cited by 179
Metadata
- Authors
- Watt, M. J., & Hoy, A. J.
- Affiliations
- Monash University (AU)
- Corresponding author
- Watt, Matthew J.
- Venue
- American Journal of Physiology-Endocrinology and Metabolism
- Publisher
- American Physiological Society
- Published
- 2012-06-01
- Volume
- 302
- Issue
- 11
- Pages
- E1315-E1328
- ISSN
- 0193-1849 (ISSN-L)
- 1522-1555
- OpenAlex
- W2033804400
- Cited by
- 142
- References
- 208
- Citations by year
- 2026: 5 · 2025: 13 · 2024: 15 · 2023: 7 · 2022: 9 · 2021: 13 · 2020: 11 · 2019: 15 · 2018: 7 · 2017: 3 · 2016: 6 · 2015: 11 · 2014: 9 · 2013: 11 · 2012: 7
- FWCI
- 0.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- skeletal muscle lipid metabolism, fatty acid metabolism, lipolysis, de novo lipogenesis, lipid droplets, mitochondrial fatty acid oxidation, fatty acid beta-oxidation, lipid signaling, insulin action, adipose tissue lipolysis, membrane lipids
- MeSH terms
- Adaptation, Physiological, Animals, Fatty Acids, Humans, Insulin Resistance, Lipids, Triglycerides, Signal Transduction, Muscle, Skeletal, Muscle Fibers, Skeletal, Lipid Metabolism
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.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
