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Development of Muscle Insulin Resistance After Liver Insulin Resistance in High-Fat–Fed Rats
Abstract
Muscle and hepatic insulin resistance are two major defects of non-insulin-dependent diabetes mellitus. Dietary factors may be important in the etiology of insulin resistance. We studied progressive changes in the development of high-fat–diet–induced insulin resistance in tissues of the adult male Wistar rat. In vivo insulin action was compared 3 days and 3 wk after isocaloric synthetic high-fat or high-starch feeding (59 and 10% cal as fat, respectively). Basal and insulin-stimulated glucose metabolism were assessed in the conscious 5- to 7-h fasted state with the euglycemic clamp (600 pM insulin) with a [3-3H]-glucose infusion. Fat feeding significantly reduced suppressibility of hepatic glucose output by insulin after both 3 days and 3 wk of diet (P < 0.01). However, a significant impairment of insulin-mediated peripheral glucose disposal was only present after 3 wk of diet. Further in vivo [3H]-2-deoxyglucose uptake studies supported this finding and demonstrated adipose but not muscle insulin resistance after 3 days of high-fat feeding. Muscle triglyceride accumulation due to fat feeding was not significant at 3 days but had doubled by 3 wk in red muscle (P < 0.001) compared with starch-fed controls. By 3 wk, high-fat—fed animals had developed significant glucose intolerance. We concludethat fat feeding induces insulin resistance in liver and adipose tissue before skeletal muscle with early metabolic changes favoring an oversupply of energy substrate to skeletal muscle relative to metabolic needs. This may generate later muscle insulin resistance.
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“Three days of high-fat feeding in rats results specifically in hepatic steatosis and hepatic insulin resistance.”
From Inhibition of protein kinase Cε prevents hepatic insulin resistance in nonalcoholic fatty liver disease (2007) · cites this paper as [13]
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Short Term Voluntary Overfeeding Disrupts Brain Insulin Control of Adipose Tissue Lipolysis
Scherer, T., Lindtner, C., Zieliński, E., O’Hare, J., Filatova, N., & Buettner, C. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.307348 · Cited by 72
“Short term overfeeding is sufficient to induce hepatic insulin resistance (16, 17, 32).”
BackgroundDynamic Metabolomics Reveals that Insulin Primes the Adipocyte for Glucose Metabolism
Krycer, J. R., Yugi, K., Hirayama, A., Fazakerley, D. J., Quek, L., Scalzo, R. A., Ohno, S., Hodson, M. P., Ikeda, S., Shoji, F., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.11.085 · Cited by 70
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“For example, male Wistar and Sprague Dawley rats consuming a diet with 59% of energy from fat developed hepatic but not muscle insulin resistance after 3 days [2, 32].”
MethodPark, S., Hong, S. M., Lee, J. E., & Sung, S. R. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00434.2007 · Cited by 68
“Diets high in fat have been well known to increase insulin resistance, which results in the development and/or exacerbation of Type 2 diabetes (19, 32).”
BackgroundInsulin Resistance, Obesity, and Lipotoxicity
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Study of iron metabolism disturbances in an animal model of insulin resistance
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Insulin Action, Regional Fat, and Myocyte Lipid: Altered Relationships with Increased Adiposity
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“It was found that he rats fed high fat diets had significantly higher fasting plasma nsulin and glucose levels compared to control animals, characterstic symptoms of insulin resistance (Kraegen et al. 1991).”
BackgroundIntrinsic aerobic capacity impacts susceptibility to acute high-fat diet-induced hepatic steatosis
Morris, E. M., Jackman, M. R., Johnson, G. C., Cross, T.-W., Lopez, J. L., Kearney, M. L., Fletcher, J. A., Meers, G. M.-E., Koch, L. G., Britton, S. L., et al. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00093.2014 · Cited by 69
“induce obesity, steatosis, and insulin resistance (14, 20).”
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“This inflammation is believed to contribute to insulin resistance not only in the adipose tissue [4] but also in liver and skeletal muscle [5], and thereby aggravates the diabetic state.”
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Sources of hepatic triglyceride accumulation during high‐fat feeding in the healthy rat
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Fatty Acid and Glucose Sensors in Hepatic Lipid Metabolism: Implications in NAFLD
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Insulin signaling requires glucose to promote lipid anabolism in adipocytes
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“For example, in high fat diet fed rats, insulin resistance was found to initiate in the liver, prior to developing in skeletal muscle.(26) In addition, impairment in all steps of insulin signaling was detected in skeletal muscle, liver, hypothalamus, but not in adipose tissue of fat-rich diet treated mice.”
BackgroundModulation of triglyceride metabolism by glucocorticoids in diet-induced obesity
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“The fat component of the diet was mainly involved in the development of insulin resistance (32), with some contribution from sucrose (40).”
BackgroundBeyond Diabetes: Does Obesity-Induced Oxidative Stress Drive the Aging Process?
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“A deficient cellular response to insulin is thought to be the primary deficit associated with obesity and fat accumulation with the main tissues of significance in glucose metabolism being skeletal muscle, liver and adipose tissue [75,76].”
Subcutaneous adipose tissue accumulation protects systemic glucose tolerance and muscle metabolism
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Neferine enhances insulin sensitivity in insulin resistant rats
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Natural products: Regulating glucose metabolism and improving insulin resistance
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Metadata
- Authors
- Kraegen, E. W., Clark, P. W., Jenkins, A. B., Daley, E. A., Chisholm, D. J., & Storlien, L. H.
- Affiliations
- Garvan Institute of Medical Research (AU)
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 1991-11-01
- Volume
- 40
- Issue
- 11
- Pages
- 1397-1403
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- OpenAlex
- W2049881486
- Cited by
- 601
- References
- 0
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 10 · 2023: 11 · 2022: 14 · 2021: 7 · 2020: 13 · 2019: 22 · 2018: 18 · 2017: 17 · 2016: 37 · 2015: 22 · 2014: 37 · 2013: 31 · 2012: 27
- FWCI
- 2.59
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Health and Medical Research Council
- National Medical Research Council
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diet, Metabolism, and Disease
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- insulin resistance, high-fat diet, hepatic insulin resistance, skeletal muscle insulin resistance, adipose tissue insulin resistance, hepatic glucose production, impaired glucose tolerance, type 2 diabetes, dietary fat
- MeSH terms
- Animals, Dietary Fats, Glucose, Insulin, Insulin Resistance, Liver, Male, Muscles, Rats, Inbred Strains, Starch, Triglycerides, Rats
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