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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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BackgroundPre-Exercise High-Fat Diet for 3 Days Affects Post-Exercise Skeletal Muscle Glycogen Repletion
Takahashi, Y., Matsunaga, Y., Tamura, Y., Terada, S., & Hatta, H. (2017) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.63.323 · Cited by 6
Impact of Short-Term Lipid Overload on Whole-Body Physiology
Keles, U., Kalem-Yapar, N. E., Hultén, H., Zhao, L. N., & Kaldis, P. (2024) · Molecular and Cellular Biology · doi:10.1080/10985549.2024.2438814 · Cited by 7
“49 This indicates that lipid deposition blunts the ability of insulin to stimulate glycogen synthesis in the liver, which is the main pathway to remove glucose from circulation and store it in the liver.”
Clematis chinensis Extract Protects against Diabetic Nephropathy in Rats
Xu, L., Zhao, B. T., Sun, J., et al. (2016) · Tropical Journal of Pharmaceutical Research · doi:10.4314/tjpr.v15i3.12 · Cited by 5
“Consuming an HFD can induce insulin resistance [15], primarily through the Randle or glucosefatty acid cycle [16].”
BackgroundMetabolic Effects of Short-Term High-Fat Intake Vary Depending on Dietary Amino Acid Composition
Nishi, H., Goda, Y., Okino, R., Iwai, R., Maezawa, R., Ito, K., Takahashi, S.-I., Yamanaka, D., & Hakuno, F. (2024) · Current Developments in Nutrition · doi:10.1016/j.cdnut.2024.103768 · Cited by 6
“…insulin-receptor phosphorylation in the liver, skeletal muscle, and adipose tissue can be observed after 14 d of HFD feeding in Sprague-Dawley rats, and insulin-sensitivity of hepatic sugar metabolic control is impaired within only 3 d after initiation of HFD feeding in Wistar rats [19 – 21].”
MethodAntiobesity actions of Embelia ribes
Nazish, I., Ansari, S., & Arora, P. (2012) · Pharmacognosy Journal · doi:10.5530/pj.2012.32.13 · Cited by 5
“We selected a rat model of diet induced obesity based on numerous experimental studies indicated that consumption of HFD leads to increased body weight and fat mass, induce alterations in carbohydrate and lipid metabolism, lead to insulin resistance, increase production and release of leptin in laboratory animals and…”
MethodSequence of fat partitioning and its relationship with whole body insulin resistance.
Xp, B., Hl, L., Yang, W.-Y., Jz, X., Wang, B., Lou, D.-J., & Rq, D. (2010) · PubMed · Cited by 5
Jacobs, D. T., Allard, B. A., Pottorf, T. S., Silva, L. M., Wang, W., Al‐Naamani, A., Agborbesong, E., Wang, T., Carr, D. A., & Tran, P. V. (2019) · The FASEB Journal · doi:10.1096/fj.201900751r · Cited by 5
Tian, L., Syed‐Abdul, M. M., Stahel, P., & Lewis, G. F. (2022) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00095.2022 · Cited by 5
Non Alcoholic Fatty Liver Overview
Debes, M. S. (2015) · Journal of Liver · doi:10.4172/2167-0889.1000177 · Cited by 5
“The loss of balance between energy intake and output seems to play critical part in the inappropriate fat storage in the liver and this was demonstrated in animal studies which showed insulin resistance in liver and adipose tissue followed by skeletal muscles when energy substrates supply exceeded the actual consumpti…”
BackgroundLee, Y. J., Jeong, J., Kim, M. O., et al. (2016) · Han-guk hyeonmigyeong hakoeji/Applied microscopy · doi:10.9729/am.2016.46.3.140 · Cited by 5
“Moreover, sugar consumption and intake related to insulin resistance (Kraegen et al., 1991; Luo et al., 1995; Nakamura et al., 2001; Storlien et al., 1991) also increased due to high income levels and availability of processed foods (Bray et al., 2004).”
BackgroundYaturramadhan, H., Dalimunthe, A., & Widyawati, T. (2019) · Asian Journal of Pharmaceutical Research and Development · doi:10.22270/ajprd.v7i4.548 · Cited by 5
Hépatopathie non alcoolique: de la stéatose à la cirrhose
Leclercq, I. A., & Sempoux, C. L. (2006) · Acta Endoscopica · doi:10.1007/bf03006037 · Cited by 5
“responsable de l'insulinor6sistance intra-h6patique [65-68].”
Fibre Type Dependent Expression of Glucose Transporters in Human Skeletal Muscles
Gaster, M. (2007) · Apmis · doi:10.1111/j.1600-0463.2007.apm_v115_s121.x · Cited by 5
Hormonal and nutritional modulation of PDHC activity status
Sugden, M. C., & Holness, M. J. (1996) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8981-0_12 · Cited by 5
Hupfeld, C. J., & Olefsky, J. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-18907-1.00040-8 · Cited by 7
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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