Skeletal muscle fiber type-selective effects of acute exercise on insulin-stimulated glucose uptake in insulin-resistant, high-fat-fed rats

Mechanisms for Insulin Resistance: Common Threads and Missing Links

Samuel, V. T., & Shulman, G. I. (2012) · Cell · doi:10.1016/j.cell.2012.02.017 · Cited by 2,294 · see citing works

The Effect of Insulin on the Disposal of Intravenous Glucose: Results from Indirect Calorimetry and Hepatic and Femoral Venous Catheterization

DeFronzo, R. A., Jacot, E., Jequier, E., Maeder, E., Wahren, J., & Felber, J. P. (1981) · Diabetes · doi:10.2337/diab.30.12.1000 · Cited by 1,770 · see citing works

The GLUT4 Glucose Transporter

Huang, S., & Czech, M. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.03.006 · Cited by 1,399 · see citing works

Intramyocellular lipid concentrations are correlated with insulin sensitivity in humans: a 1 H NMR spectroscopy study

Krssak, M., Falk Petersen, K., Dresner, A., DiPietro, L., Vogel, S. M., Rothman, D. L., Shulman, G. I., & Roden, M. (1999) · Diabetologia · doi:10.1007/s001250051123 · Cited by 1,264 · see citing works

Skeletal muscle lipid content and insulin resistance: evidence for a paradox in endurance-trained athletes

Goodpaster, B. H. (2001) · Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.86.12.5755 · Cited by 1,194 · see citing works

Cellular and molecular diversities of mammalian skeletal muscle fibers

Pette, D., & Staron, R. S. (1990) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/3540528806_3 · Cited by 798 · see citing works

Increased glucose transport-phosphorylation and muscle glycogen synthesis after exercise training in insulin-resistant subjects

Perseghin, G., Price, T. B., Petersen, K. F., Roden, M., Cline, G. W., Gerow, K., Rothman, D. L., & Shulman, G. I. (1996) · New England Journal of Medicine · doi:10.1056/nejm199610313351804 · Cited by 699 · see citing works

Rapid Determination of Myosin Heavy Chain Expression in Rat, Mouse, and Human Skeletal Muscle Using Multicolor Immunofluorescence Analysis

Bloemberg, D., & Quadrilatero, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035273 · Cited by 613 · see citing works

Insulin resistance as a predictor of age-related diseases

Facchini, F. S., Hua, N., Abbasi, F., & Reaven, G. M. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.8.7763 · Cited by 594 · see citing works

Muscle Glucose Metabolism following Exercise in the Rat

Richter, E. A., Garetto, L. P., Goodman, M. N., & Ruderman, N. B. (1982) · Journal of Clinical Investigation · doi:10.1172/jci110517 · Cited by 510 · see citing works

Evidence for defects in the trafficking and translocation of GLUT4 glucose transporters in skeletal muscle as a cause of human insulin resistance

Garvey, W. T., Maianu, L., Zhu, J. H., Brechtel-Hook, G., Wallace, P., & Baron, A. D. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1557 · Cited by 459 · see citing works

Distinct patterns of tissue-specific lipid accumulation during the induction of insulin resistance in mice by high-fat feeding

Turner, N., Kowalski, G. M., Leslie, S. J., Risis, S., Yang, C., Lee-Young, R. S., Babb, J. R., Meikle, P. J., Lancaster, G. I., Henstridge, D. C., et al. (2013) · Diabetologia · doi:10.1007/s00125-013-2913-1 · Cited by 430 · see citing works

Insulin signaling and insulin sensitivity after exercise in human skeletal muscle

Wojtaszewski, J. F., Hansen, B. F., Gade, Kiens, B., Markuns, J. F., Goodyear, L. J., & Richter, E. A. (2000) · Diabetes · doi:10.2337/diabetes.49.3.325 · Cited by 382 · see citing works

Effect of exercise on insulin action in human skeletal muscle

Richter, E. A., Mikines, K. J., Galbo, H., & Kiens, B. (1989) · Journal of Applied Physiology · doi:10.1152/jappl.1989.66.2.876 · Cited by 357 · see citing works

Prolonged increase in insulin-stimulated glucose transport in muscle after exercise

Cartee, G. D., Young, D. A., Sleeper, M. D., Zierath, J., Wallberg-Henriksson, H., & Holloszy, J. O. (1989) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1989.256.4.e494 · Cited by 342 · see citing works

Enhanced Peripheral and Splanchnic Insulin Sensitivity in NIDDM Men After Single Bout of Exercise

Devlin, J. T., Hirshman, M., Horton, E. D., & Horton, E. S. (1987) · Diabetes · doi:10.2337/diab.36.4.434 · Cited by 342 · see citing works

Role of intramyocelluar lipids in human health

Coen, P. M., & Goodpaster, B. H. (2012) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2012.05.009 · Cited by 252 · cited 1× · see citing works

Lipid Mediators of Insulin Resistance

Holland, W. L., Knotts, T. A., Chavez, J. A., Wang, L., Hoehn, K. L., & Summers, S. A. (2007) · Nutrition Reviews · doi:10.1301/nr.2007.jun.s39-s46 · Cited by 251 · see citing works

High-Fat Feeding Impairs Insulin-Stimulated GLUT4 Recruitment via an Early Insulin-Signaling Defect

Zierath, J. R., Houseknecht, K. L., Gnudi, L., & Kahn, B. B. (1997) · Diabetes · doi:10.2337/diab.46.2.215 · Cited by 238 · see citing works

LSDP5 is a PAT protein specifically expressed in fatty acid oxidizing tissues

Dalen, K. T., Dahl, T. B., Holter, E., Arntsen, B. M., Londos, C., Sztalryd, C., & Nebb, H. I. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2006.11.011 · Cited by 236 · see citing works

Glucose transport into rat skeletal muscle: interaction between exercise and insulin

Wallberg‐Henriksson, H., Constable, S. H., Young, D. A., & Holloszy, J. O. (1988) · Journal of Applied Physiology · doi:10.1152/jappl.1988.65.2.909 · Cited by 210 · see citing works

Effects of Prior High-Intensity Exercise on Glucose Metabolism in Normal and Insulin-resistant Men

Devlin, J. T., & Horton, E. S. (1985) · Diabetes · doi:10.2337/diab.34.10.973 · Cited by 207 · see citing works

Insulin Signaling in Human Skeletal Muscle: Time Course and Effect of Exercise

Wojtaszewski, J. F. P., Hansen, B. F., Kiens, B., & Richter, E. A. (1997) · Diabetes · doi:10.2337/diab.46.11.1775 · Cited by 206 · see citing works

Enhanced muscle glucose metabolism after exercise in the rat: the two phases

Garetto, L. P., Richter, E. A., Goodman, M. N., & Ruderman, N. B. (1984) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1984.246.6.e471 · Cited by 198 · see citing works

Intracellular localization of diacylglycerols and sphingolipids influences insulin sensitivity and mitochondrial function in human skeletal muscle

Perreault, L., Newsom, S. A., Strauss, A., Kerege, A., Kahn, D. E., Harrison, K. A., Snell-Bergeon, J. K., Nemkov, T., D’Alessandro, A., Jackman, M. R., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.96805 · Cited by 184 · see citing works

Epidemiology of insulin resistance and its relation to coronary artery disease

Haffner, S. M. (1999) · The American Journal of Cardiology · doi:10.1016/s0002-9149(99)00351-3 · Cited by 173 · see citing works

Increased subsarcolemmal lipids in type 2 diabetes: effect of training on localization of lipids, mitochondria, and glycogen in sedentary human skeletal muscle

Nielsen, J., Mogensen, M., Vind, B. F., Sahlin, K., Højlund, K., Schrøder, H. D., & Ørtenblad, N. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00692.2009 · Cited by 158 · see citing works

Roles of TBC1D1 and TBC1D4 in insulin- and exercise-stimulated glucose transport of skeletal muscle

Cartee, G. D. (2014) · Diabetologia · doi:10.1007/s00125-014-3395-5 · Cited by 153 · see citing works

Reduction in hybrid single muscle fiber proportions with resistance training in humans

Williamson, D. L., Gallagher, P. M., Carroll, C. C., Raue, U., & Trappe, S. W. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.5.1955 · Cited by 150 · see citing works

Lipid Mediators of Insulin Resistance

Holland, W. L., Knotts, T. A., Chavez, J. A., Wang, L.-P., Hoehn, K. L., & Summers, S. A. (2008) · Nutrition Reviews · doi:10.1111/j.1753-4887.2007.tb00327.x · Cited by 147 · see citing works

A High Fat Diet Impairs Stimulation of Glucose Transport in Muscle

Hansen, P. A., Han, D. H., Marshall, B. A., Nolte, L. A., Chen, M. M., Mueckler, M. M., & Holloszy, J. O. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.40.26157 · Cited by 141 · see citing works

Mechanisms for greater insulin-stimulated glucose uptake in normal and insulin-resistant skeletal muscle after acute exercise

Cartee, G. D. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00416.2015 · Cited by 140 · see citing works

Use of BODIPY (493/503) to Visualize Intramuscular Lipid Dropletsin Skeletal Muscle

Spangenburg, E. E., Pratt, S. J. P., Wohlers, L. M., & Lovering, R. M. (2011) · BioMed Research International · doi:10.1155/2011/598358 · Cited by 139 · see citing works

Increased Muscle Glucose Uptake After Exercise: No Need for Insulin During Exercise

Richter, E. A., Ploug, T., & Galbo, H. (1985) · Diabetes · doi:10.2337/diab.34.10.1041 · Cited by 135 · see citing works

Increased AS160 phosphorylation, but not TBC1D1 phosphorylation, with increased postexercise insulin sensitivity in rat skeletal muscle

Funai, K., Schweitzer, G. G., Sharma, N., Kanzaki, M., & Cartee, G. D. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00194.2009 · Cited by 119 · see citing works

Prior exercise increases phosphorylation of Akt substrate of 160 kDa (AS160) in rat skeletal muscle

Arias, E. B., Kim, J., Funai, K., & Cartee, G. D. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00602.2006 · Cited by 118 · see citing works

Acute exercise and GLUT4 expression in human skeletal muscle: influence of exercise intensity

Kraniou, G. N., Cameron‐Smith, D., & Hargreaves, M. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01489.2005 · Cited by 117 · see citing works

Insulin Resistance of Muscle Glucose Transport in Rats Fed a High-Fat Diet: A Reevaluation

Han, D., Hansen, P. A., Host, H. H., & Holloszy, J. O. (1997) · Diabetes · doi:10.2337/diab.46.11.1761 · Cited by 117 · see citing works

Ca2+ activation of diffusible and bound pools of μ‐calpain in rat skeletal muscle

Murphy, R. M., Verburg, E., & Lamb, G. D. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.114090 · Cited by 114 · see citing works

Glycogen depletion in rat skeletal muscle fibers at different intensities and durations of excercise

Armstrong, R. B., Saubert, C. W., Sembrowich, W. L., SHEPHERD, R. E., & Gollnick, P. D. (1974) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00590489 · Cited by 114 · see citing works

Exercise Alleviates Lipid-Induced Insulin Resistance in Human Skeletal Muscle–Signaling Interaction at the Level of TBC1 Domain Family Member 4

Pehmøller, C. K., Brandt, N., Birk, J. B., Høeg, L. D., Sjøberg, K. A., Goodyear, L. J., Kiens, B., Richter, E. A., & Wojtaszewski, J. F. P. (2012) · Diabetes · doi:10.2337/db11-1572 · Cited by 103 · see citing works

Minireview: Mechanisms by Which the Metabolic Syndrome and Diabetes Impair Memory

Meena Kumari, B., Brunner, E. J., & Fuhrer, R. (2000) · The Journals of Gerontology Series A · doi:10.1093/gerona/55.5.b228 · Cited by 102 · see citing works

Proceedings of the Australian Physiological and Pharmacological Society Symposium: New Frontiers in Muscle Research Hybrid skeletal muscle fibres: a rare or common phenomenon?

Stephenson, G. M. M. (2001) · Clinical and Experimental Pharmacology and Physiology · doi:10.1046/j.1440-1681.2001.03505.x · Cited by 101 · see citing works

Single-fiber myosin heavy chain polymorphism: how many patterns and what proportions?

Caiozzo, V. J., Baker, M. J., Huang, K., Chou, H., Wu, Y. Z., & Baldwin, K. M. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00646.2002 · Cited by 95 · see citing works

Postexercise Improvement in Insulin-Stimulated Glucose Uptake Occurs Concomitant With Greater AS160 Phosphorylation in Muscle From Normal and Insulin-Resistant Rats

Castorena, C. M., Arias, E. B., Sharma, N., & Cartee, G. D. (2014) · Diabetes · doi:10.2337/db13-1686 · Cited by 87 · see citing works

Increased submaximal insulin-stimulated glucose uptake in mouse skeletal muscle after treadmill exercise

Hamada, T., Arias, E. B., & Cartee, G. D. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00416.2006 · Cited by 84 · see citing works

A modified PAS stain combined with immunofluorescence for quantitative analyses of glycogen in muscle sections

Schaart, G., Hesselink, R., KEIZER, H. A., van Kranenburg, G., Drost, M., & Hesselink, M. K. C. (2004) · Histochemistry and Cell Biology · doi:10.1007/s00418-004-0690-0 · Cited by 79 · see citing works

Enhanced technique to measure proteins in single segments of human skeletal muscle fibers: fiber-type dependence of AMPK-α1 and -β1

Murphy, R. M. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01082.2010 · Cited by 78 · see citing works

Relative Contribution of Intramyocellular Lipid to Whole-Body Fat Oxidation Is Reduced With Age but Subsarcolemmal Lipid Accumulation and Insulin Resistance Are Only Associated With Overweight Individuals

Chee, C., Shannon, C. E., Burns, A., Selby, A. L., Wilkinson, D., Smith, K., Greenhaff, P. L., & Stephens, F. B. (2016) · Diabetes · doi:10.2337/db15-1383 · Cited by 74 · see citing works

Effects of exercise on insulin binding and glucose metabolism in muscle

Bonen, A., Tan, M. H., & Watson-Wright, W. M. (1984) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y84-248 · Cited by 72 · see citing works

PET imaging reveals distinctive roles for different regional adipose tissue depots in systemic glucose metabolism in nonobese humans

Ng, J. M., Azuma, K., Kelley, C. A., Pencek, R., Rádiková, Ž., Laymon, C. M., Price, J. C., Goodpaster, B. H., & Kelley, D. E. (2012) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00282.2012 · Cited by 67 · see citing works

Muscle glucose metabolism in exercising rats: comparison with insulin stimulation

James, D. E., Kraegen, E. W., & Chisholm, D. J. (1985) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1985.248.5.e575 · Cited by 66 · see citing works

Lipid droplet size and location in human skeletal muscle fibers are associated with insulin sensitivity

Nielsen, J., Christensen, A. E., Nellemann, B., & Christensen, B. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00062.2017 · Cited by 50 · see citing works

Sustained postexercise increases in AS160 Thr642and Ser588phosphorylation in skeletal muscle without sustained increases in kinase phosphorylation

Schweitzer, G. G., Arias, E. B., & Cartee, G. D. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00619.2012 · Cited by 47 · see citing works

Measuring GLUT4 translocation in mature muscle fibers

Lauritzen, H. P. M. M., & Schertzer, J. D. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00066.2010 · Cited by 43 · see citing works

A Novel Method to Measure Glucose Uptake and Myosin Heavy Chain Isoform Expression of Single Fibers From Rat Skeletal Muscle

MacKrell, J. G., & Cartee, G. D. (2012) · Diabetes · doi:10.2337/db11-1299 · Cited by 42 · see citing works

High-Fat Diet-Induced Insulin Resistance in Single Skeletal Muscle Fibers is Fiber Type Selective

Pataky, M. W., Wang, H., Yu, C. S., Arias, E. B., Ploutz-Snyder, R. J., Zheng, X., & Cartee, G. D. (2017) · Scientific Reports · doi:10.1038/s41598-017-12682-z · Cited by 38 · see citing works

Increased insulin‐stimulated glucose uptake by exercised human muscles one day after prolonged physical exercise

Annuzzi, G., Riccardi, G., Capaldo, B., & Kauser, L. (1991) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.1991.tb01351.x · Cited by 37 · see citing works

The continuum of hybrid IIX/IIB fibers in normal mouse muscles: MHC isoform proportions and spatial distribution within single fibers

Zhang, M. Y., Zhang, W. J., & Medler, S. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00402.2010 · Cited by 36 · see citing works

Novel single skeletal muscle fiber analysis reveals a fiber type-selective effect of acute exercise on glucose uptake

Cartee, G. D., Arias, E. B., Yu, C. S., & Pataky, M. W. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00289.2016 · Cited by 27 · see citing works

Postexercise improvement in glucose uptake occurs concomitant with greater γ3-AMPK activation and AS160 phosphorylation in rat skeletal muscle

Wang, H., Arias, E. B., Pataky, M. W., Goodyear, L. J., & Cartee, G. D. (2018) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00020.2018 · Cited by 26 · see citing works

Fiber Type-Specific Differences in Glucose Uptake by Single Fibers From Skeletal Muscles of 9- and 25-Month-Old Rats

MacKrell, J. G., Arias, E. B., & Cartee, G. D. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls194 · Cited by 25 · see citing works

Exercise-induced glycogen utilization by the respiratory muscles

Ianuzzo, C. D., Spalding, M. J., & Williams, H. (1987) · Journal of Applied Physiology · doi:10.1152/jappl.1987.62.4.1405 · Cited by 19 · see citing works

Discordance between intramuscular triglyceride and insulin sensitivity in skeletal muscle of Zucker diabetic rats after treatment with fenofibrate and rosiglitazone

Nadeau, K. J., Ehlers, L. B., Aguirre, L. E., Reusch, J. E. B., & Draznin, B. (2007) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2006.00696.x · Cited by 19 · see citing works

Relative degree of stimulation‐evoked glycogen degradation in muscle fibres of different type in rat gastrocnemius.

Kernell, D., Lind, A., van Diemen, A. B., & HAAN, A. D. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020653 · Cited by 16 · see citing works

Duration of Improved Muscle Glucose Uptake After Acute Exercise in Obese Zucker Rats

Betts, J. J., Sherman, W. M., Reed, M. J., & Gao, J. (1993) · Obesity Research · doi:10.1002/j.1550-8528.1993.tb00624.x · Cited by 13 · see citing works

Using a novel coculture model to dissect the role of intramuscular lipid load on skeletal muscle insulin responsiveness under reduced estrogen conditions

Wohlers, L. M., Powers, B. L., Chin, E. R., & Spangenburg, E. E. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00617.2012 · Cited by 11 · see citing works

Activation of muscle fibers in individual motor units revealed by 2- deoxyglucose-6-phosphate

Nemeth, P. M., Norris, B., Lowry, O. H., Gordon, D., Enoka, R. M., & Dg, S. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-11-03959.1988 · Cited by 8 · see citing works

Measuring Both Glucose Uptake and Myosin Heavy Chain Isoform Expression in Single Rat Skeletal Muscle Fibers

Pataky, M. W., Arias, E. B., & Cartee, G. D. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8897-6_17 · Cited by 8 · see citing works

The many actions of insulin in skeletal muscle, the paramount tissue determining glycemia

Sylow, L., Tokarz, V. L., Richter, E. A., & Klip, A. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.03.020 · Cited by 366 · see citing works

Hormonal and Metabolic Changes of Aging and the Influence of Lifestyle Modifications

Pataky, M. W., Young, W. F., & Nair, K. S. (2021) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2020.07.033 · Cited by 207 · see citing works

Understanding glycaemic control and current approaches for screening antidiabetic natural products from evidence-based medicinal plants

Lankatillake, C., Huynh, T. T., & Dias, D. A. (2019) · Plant Methods · doi:10.1186/s13007-019-0487-8 · Cited by 159 · see citing works

Roles of Alkaloids from Medicinal Plants in the Management of Diabetes Mellitus

Adhikari, B. (2021) · Journal of Chemistry · doi:10.1155/2021/2691525 · Cited by 83 · see citing works

High Fat Rodent Models of Type 2 Diabetes: From Rodent to Human

Stott, N. L., & Marino, J. S. (2020) · Nutrients · doi:10.3390/nu12123650 · Cited by 73 · see citing works

Glucose transporter 4: Insulin response mastermind, glycolysis catalyst and treatment direction for cancer progression

Chang, Y., Chan, M., Yang, Y., Li, C., & Hsiao, M. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216179 · Cited by 77 · see citing works

Transcriptome profiling of fast/glycolytic and slow/oxidative muscle fibers in aging and obesity

Zhang, F., Wu, H.-F., Wang, K., Yu, D., Zhang, X.-Z., Ren, Q., Chen, W., Lin, F., Yu, Z., & Zhuang, C.-L. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06851-y · Cited by 42 · see citing works

Physical exercise, health, and disease treatment: The role of macrophages

Callegari, I. O. M., Rocha, G. Z., & Oliveira, A. G. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1061353 · Cited by 29 · see citing works

The Change of Skeletal Muscle Caused by Inflammation in Obesity as the Key Path to Fibrosis: Thoughts on Mechanisms and Intervention Strategies

Li, Y., Guo, W., Li, H., Wang, Y., Liu, X., & Kong, W. (2024) · Biomolecules · doi:10.3390/biom15010020 · Cited by 28 · see citing works

Muscle fiber type-dependence effect of exercise on genomic networks in aged mice models

Lee, S. M., Lee, M. C., Bae, W. R., Yoon, K. J., & Moon, H. Y. (2022) · Aging · doi:10.18632/aging.204024 · Cited by 22 · see citing works

A maternal high-fat/low-fiber diet impairs glucose tolerance and induces the formation of glycolytic muscle fibers in neonatal offspring

Hu, C., Yang, Y., Chen, M., Hao, X., Wang, S., Yang, L., Yin, Y., & Tan, C. (2021) · European Journal of Nutrition · doi:10.1007/s00394-020-02461-4 · Cited by 19 · see citing works

Short-term high-fat diet induces muscle fiber type-selective anabolic resistance to resistance exercise

Ato, S., Mori, T., Fujita, Y., Mishima, T., & Ogasawara, R. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00889.2020 · Cited by 12 · see citing works

Exercise effects on γ3-AMPK activity, Akt substrate of 160 kDa phosphorylation, and glucose uptake in muscle of normal and insulin-resistant female rats

Wang, H., Arias, E. B., Treebak, J. T., & Cartee, G. D. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00533.2021 · Cited by 11 · see citing works

Exercise effects on γ3-AMPK activity, phosphorylation of Akt2 and AS160, and insulin-stimulated glucose uptake in insulin-resistant rat skeletal muscle

Pataky, M. W., Arias, E. B., Wang, H., Zheng, X., & Cartee, G. D. (2020) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00428.2019 · Cited by 11 · see citing works

Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle

Pataky, M. W., Acker, S. L. V., Dhingra, R., Freeburg, M. M., Arias, E. B., Oki, K., Wang, H., Treebak, J. T., & Cartee, G. D. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00304.2019 · Cited by 9 · see citing works

Effect of Regular Exercise on Fat Metabolism in Rats Fed on Zinc Picolinate Supplemented Diet

Erdoğan, R., Tel, M., Çınar, V., & Pala, R. (2021) · Pakistan Journal of Zoology · doi:10.17582/journal.pjz/20210328140341 · Cited by 6 · see citing works

Exercise improves high-fat diet-induced metabolic disorder by promoting HDAC5 degradation through the ubiquitin–proteasome system in skeletal muscle

Huang, S. M., Zheng, X., Zhang, X., Jin, Z., Liu, S., Fu, L., & Niu, Y. (2022) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2022-0174 · Cited by 6 · see citing works

Genomics and transcriptomics landscapes associated to changes in insulin sensitivity in response to endurance exercise training

Takeshita, L. Y. C., Davidsen, P. K., Herbert, J. M. J., Antczak, P., Hesselink, M. K. C., Schrauwen, P., Weisnagel, S. J., Robbins, J., Gerszten, R. E., Ghosh, S., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-98792-1 · Cited by 6 · see citing works

Effect of Resveratrol in Melinjo Seed (Gnetum gnemon L.) Extract on Type 2 Diabetes Mellitus Patients and its Possible Mechanism: A Review

Ariyanto, E. F., Danil, A. S., Rohmawaty, E., Sujatmiko, B., & Berbudi, A. (2022) · Current Diabetes Reviews · doi:10.2174/1573399818666220228160908 · Cited by 5 · see citing works

Exercise does not improve insulin resistance and mitochondrial characteristics together

Genders, A. J., Kuang, J., Marin, E. C., Saner, N. J., Botella, J., Jacques, M., McConell, G. K., Andrade-Souza, V. A., Chagolla, J., & Bishop, D. J. (2021) · Journal of Endocrinology · doi:10.1530/joe-21-0242 · Cited by 4 · see citing works

Evaluation of the toxicity potential of exercise and atorvastatin/metformin combination therapy on STZ-diabetic rats

Tunçyürekli, M., Tülüce, Y., & Lermioǧlu, F. (2024) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-024-03663-x · Cited by 2 · see citing works

Effects of different maternal feeding strategies from day 1 to day 85 of gestation on glucose tolerance and muscle development in both low and normal birth weight piglets

Hu, C., Jin, P., Yang, Y., Yang, L., Zhang, Z., Zhang, L., Yin, Y., & Tan, C. (2020) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.10591 · Cited by 2 · see citing works

Genetic reduction of skeletal muscle glycogen synthase 1 abundance reveals that the refeeding‐induced reversal of elevated insulin‐stimulated glucose uptake after exercise is not attributable to achieving a high muscle glycogen concentration

Kwak, S. E., Wang, H., Pan, X., Duan, D., & Cartee, G. D. (2024) · The FASEB Journal · doi:10.1096/fj.202401859r · Cited by 1 · see citing works

Increasing skeletal muscle mass and strength during incretin-based weight loss

Mendias, C. L., & Awan, T. M. (2026) · Obesity Pillars · doi:10.1016/j.obpill.2026.100317 · Cited by 1 · see citing works

No matter the type, when it comes to recovery all fibres are similar

Lovell, A. J. (2020) · The Journal of Physiology · doi:10.1113/jp281036 · Cited by 1 · see citing works

Changes in insulin resistance do not occur in parallel with changes in mitochondrial content and function in male ratsPreprint

Genders, A. J., Kuang, J., Marin, E. C. S., Saner, N. J., Botella, J., Jacques, M., McConell, G. K., Andrade‐Souza, V. A., Chagolla, J., & Bishop, D. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.06.190702

Acute Exercise by Insulin Resistant Rats Induces Muscle Fiber Type-selective Improvement in Insulin-stimulated Glucose Uptake

Pataky, M. W., Yu, C. S., Nie, Y., Arias, E. B., Singh, M., Ploutz-Snyder, R. J., Mendias, C. L., & Cartee, G. D. (2018) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000535905.56541.aa

Mechanisms for Exercise, High-Fat Diet, and Muscle Fiber-Type Effects on Insulin-Stimulated Glucose Uptake in Skeletal Muscle

Pataky, M. W. (2019) · Deep Blue (University of Michigan)

Novel single skeletal muscle fiber analysis reveals a fiber type-selective effect of acute exercise on glucose uptake

Cartee, G. D., Arias, E. B., Yu, C. S., & Pataky, M. W. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00289.2016 · Cited by 27 · see citing works

Fiber type-specific effects of acute exercise on insulin-stimulated AS160 phosphorylation in insulin-resistant rat skeletal muscle

Pataky, M. W., Acker, S. L. V., Dhingra, R., Freeburg, M. M., Arias, E. B., Oki, K., Wang, H., Treebak, J. T., & Cartee, G. D. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00304.2019 · Cited by 9 · see citing works

A persistent increase in insulin-stimulated glucose uptake by both fast-twitch and slow-twitch skeletal muscles after a single exercise session by old rats

Xiao, Y., Sharma, N., Arias, E. B., Castorena, C. M., & Cartee, G. D. (2012) · AGE · doi:10.1007/s11357-012-9383-0 · Cited by 28 · see citing works