The DOI matches its Crossref record.
Alterations in the Expression and Cellular Localization of Protein Kinase C Isozymes ε and θ Are Associated With Insulin Resistance in Skeletal Muscle of the High-Fat–Fed Rat
Abstract
We have tested the hypothesis that changes in the levels and cellular location of protein kinase C (PKC) isozymes might be associated with the development of insulin resistance in skeletal muscles from the highfat–fed rat. Lipid measurements showed that triglyceride and diacylglycerol, an activator of PKC, were elevated four- and twofold, respectively. PKC activity assays indicated that the proportion of membraneassociated calcium-independent PKC was also increased. As determined by immunoblotting, total (particulate plus cytosolic) PKC α, ε, and ζ levels were not different between control and fat-fed rats. However, the ratio of particulate to cytosolic PKC ε in red muscles from fat-fed rats was increased nearly sixfold, suggesting chronic activation. In contrast, the amount of cytosolic PKC θ was downregulated to 45% of control, while the ratio of particulate to cytosolic levels increased, suggesting a combination of chronic activation and downregulation. Interestingly, while insulin infusion in glucose-clamped rats increased the proportion of PKC θ in the particulate fraction of red muscle, this was potentiated by fat-feeding, suggesting that the translocation is a consequence of altered lipid flux rather than a proximal event in insulin signaling. PKC ε and θ measurements from individual rats correlated with triglyceride content of red gastrocnemius muscle; they did not correlate with plasma glucose, which was not elevated in fat-fed rats, suggesting that they were not simply a consequence of hyperglycemia. Our results suggest that these specific alterations in PKC ε and PKC θ might contribute to the link between increased lipid availability and muscle insulin resistance previously described using high-fat–fed rats.
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
“Increased activity of protein kinase C (PKC-β and δ has been reported in insulin resistant states and can be induced during lipid infusion [174, 175].”
From Pathogenesis of insulin resistance in skeletal muscle (2010) · cites this paper as [174]
In the citing paper
“GLUT4, the insulin regulatable transporter, is found in skeletal muscle, has a Km of approximately 5 mmol/L, which is close to that of the plasma glucose concentration, and is associated with HK-II [173, 174].”
From Pathogenesis of insulin resistance in skeletal muscle (2010) · cites this paper as [174]
In the citing paper
“In rodents, a high-fat diet increased the concentration of diacylglycerol in muscles and activated novel PKCs.36”
From Lipid-induced insulin resistance: unravelling the mechanism (2010) · cites this paper as [36]
Citations
Cites
Still being checked.
Cited by
Sorted by citations
Items 301–314 of 314
The effect of lipids on glucoregulatory hormone actions
Grueter, E., & Alicia, C. (2006)
The role of heat shock protein 72 in preventing obesity-induced insulin resistance
Chung, J. Z. Y. (2011) · RMIT Research Repository (RMIT University Library) · doi:10.25439/rmt.27576468
Schols, A. M. W. J., & Langen, K. R. C. J. (2011)
The Effects of Chromium on Skeletal Muscle Membrane/Cytoskeletal Parameters and Insulin Sensitivity
Hoffman, N. J. (2012) · IUScholarWorks (Indiana University) · doi:10.7912/c2/1996
Bierhaus, A., & Hawroth, P. P. (2005) · Steinkopff eBooks · doi:10.1007/3-7985-1531-x_6
Treatment Regimes in Diabetes and Their Impact on Biomarkers
Magalhães, J. P., Hetherington‐Rauth, M., & Sardinha, L. B. (2022) · Biomarkers in disease · doi:10.1007/978-3-030-81303-1_3-1
Treatment Regimes in Diabetes and Their Impact on Biomarkers
Magalhães, J. P., Hetherington‐Rauth, M., & Sardinha, L. B. (2022) · Biomarkers in disease · doi:10.1007/978-3-031-08014-2_3
Role of stearoyl-CoA desaturase1 in fatty acid-induced insulin resistance
Pinnamaneni, S. (2011) · RMIT Research Repository (RMIT University Library) · doi:10.25439/rmt.27340278
Anti-diabetic effects of oleanolic acid and matrine
Zeng, X. (2014) · RMIT Research Repository (RMIT University Library) · doi:10.25439/rmt.27351540
Zarini, S., Berry, K. A. Z., Garfield, A., Macias, E., Jambal, P., Bowen, S., Cree, M. G., Snell‐Bergeon, J. K., Johnson, C., Neufer, P. D., et al. (2026) · Diabetes · doi:10.2337/db26-0239
Role of Protein Kinase C in Insulin Resistance and Metabolic Syndrome
Cruz-Villarreal, D. E., Hernández-González, K. D., & Olivares-Reyes, J. A. (2026) · Kinases and Phosphatases · doi:10.3390/kinasesphosphatases4030025
Nardi, F. (2015) · Discovery Research Portal (University of Dundee)
Stoffwechsel des Herzens bei Diabetes
Rosen, P. (2005) · Steinkopff eBooks · doi:10.1007/3-7985-1531-x_8
Metadata
- Authors
- Schmitz-Peiffer, C., Browne, C. L., Oakes, N. D., Watkinson, A., Chisholm, D. J., Kraegen, E. W., & Biden, T. J.
- Affiliations
- Garvan Institute of Medical Research Sydney, Australia
- Garvan Institute of Medical Research (AU)
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 1997-02-01
- Volume
- 46
- Issue
- 2
- Pages
- 169-178
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- OpenAlex
- W2146243104
- Cited by
- 314
- References
- 0
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 5 · 2023: 1 · 2022: 3 · 2021: 5 · 2020: 6 · 2019: 6 · 2018: 3 · 2017: 5 · 2016: 5 · 2015: 13 · 2014: 3 · 2013: 12 · 2012: 11
- FWCI
- 4.36
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Keywords
- protein kinase C, protein kinase C epsilon, PKC theta, insulin resistance, skeletal muscle, high-fat diet, diacylglycerol, triglycerides, PKC translocation, red muscle, lipid availability, insulin signaling, gastrocnemius
- MeSH terms
- Animals, Cell Compartmentation, Cytosol, Dietary Fats, Insulin, Insulin Resistance, Isoenzymes, Membranes, Protein Kinase C, Rats, Wistar, Muscle, Skeletal, Rats
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