Exercise and GLUT4

Retinol-Binding Protein 4 and Insulin Resistance in Lean, Obese, and Diabetic Subjects

Graham, T. E., Yang, Q., Blüher, M., Hammarstedt, A., Ciaraldi, T. P., Henry, R. R., Wason, C. J., Oberbach, A., Jansson, P.-A., Smith, U., et al. (2006) · New England Journal of Medicine · doi:10.1056/nejmoa054862 · Cited by 1,319 · see citing works

Adipose-selective targeting of the GLUT4 gene impairs insulin action in muscle and liver

Abel, E. D., Peroni, O. D., Kim, J. K., Kim, Y., Boss, O., Hadro, E., Minnemann, T., Shulman, G. I., & Kahn, B. B. (2001) · Nature · doi:10.1038/35055575 · Cited by 1,253 · see citing works

A Role for AMP-Activated Protein Kinase in Contraction- and Hypoxia-Regulated Glucose Transport in Skeletal Muscle

Mu, J., Brozinick, J. T., Valladares, O., Bucan, M., & Birnbaum, M. J. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00251-9 · Cited by 924 · see citing works

Low-volume high-intensity interval training reduces hyperglycemia and increases muscle mitochondrial capacity in patients with type 2 diabetes

Little, J. P., Gillen, J. B., Percival, M. E., Safdar, A., Tarnopolsky, M. A., Punthakee, Z., Jung, M. E., & Gibala, M. J. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00921.2011 · Cited by 787 · see citing works

Targeted disruption of the glucose transporter 4 selectively in muscle causes insulin resistance and glucose intolerance

Zisman, A., Peroni, O. D., Abel, E. D., Michael, M. D., Mauvais-Jarvis, F., Lowell, B. B., Wojtaszewski, J. F. P., Hirshman, M. F., Virkamaki, A., Goodyear, L. J., et al. (2000) · Nature Medicine · doi:10.1038/78693 · Cited by 743 · see citing works

Strength training increases insulin-mediated glucose uptake, GLUT4 content, and insulin signaling in skeletal muscle in patients with type 2 diabetes

Holten, M. K., Zacho, M., Gaster, M., Juel, C., Wojtaszewski, J. F. P., & Dela, F. (2004) · Diabetes · doi:10.2337/diabetes.53.2.294 · Cited by 615 · see citing works

Deficiency of LKB1 in skeletal muscle prevents AMPK activation and glucose uptake during contraction

Sakamoto, K., McCarthy, A., Smith, D. P., Green, K. A., Hardie, D. G., Ashworth, A., & Alessi, D. R. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600667 · Cited by 538 · 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

Exercise-stimulated glucose uptake — regulation and implications for glycaemic control

Sylow, L., Kleinert, M., Richter, E. A., & Jensen, T. E. (2017) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2016.162 · Cited by 498 · see citing works

Exercise-induced increase in muscle insulin sensitivity

Holloszy, J. O. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00123.2005 · Cited by 494 · see citing works

Contraction stimulates translocation of glucose transporter GLUT4 in skeletal muscle through a mechanism distinct from that of insulin

Lund, S., Holman, G. D., Schmitz, O., & Pedersen, O. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.13.5817 · Cited by 492 · see citing works

AMPK and the biochemistry of exercise: implications for human health and disease

Richter, E. A., & Ruderman, N. B. (2009) · Biochemical Journal · doi:10.1042/bj20082055 · Cited by 481 · see citing works

Muscle Glycogen Synthesis after Exercise : an Enhancing Factor localized to the Muscle Cells in Man

BERGSTRÖM, J., & HULTMAN, E. (1966) · Nature · doi:10.1038/210309a0 · Cited by 473 · see citing works

Exercise induces recruitment of the “insulin-responsive glucose transporter”. Evidence for distinct intracellular insulin- and exercise-recruitable transporter pools in skeletal muscle.

Douen, A. G., Ramlal, T., Rastogi, S., Bilan, P. J., Cartee, G. D., Vranić, M., Holloszy, J. O., & Klip, A. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)77362-6 · Cited by 471 · see citing works

AMP-activated protein kinase regulates GLUT4 transcription by phosphorylating histone deacetylase 5

McGee, S. L., van Denderen, B. J. W., Howlett, K. F., Mollica, J., Schertzer, J. D., Kemp, B. E., & Hargreaves, M. (2008) · Diabetes · doi:10.2337/db07-0843 · Cited by 455 · see citing works

Glucose transporter protein content and glucose transport capacity in rat skeletal muscles

Henriksen, E. J., Bourey, R. E., Rodnick, K. J., Koranyi, L. I., Permutt, M. A., & Holloszy, J. O. (1990) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1990.259.4.e593 · Cited by 432 · see citing works

Global Phosphoproteomic Analysis of Human Skeletal Muscle Reveals a Network of Exercise-Regulated Kinases and AMPK Substrates

Hoffman, N. J., Parker, B. L., Chaudhuri, R., Fisher-Wellman, K. H., Kleinert, M., Humphrey, S. J., Yang, P., Holliday, M., Trefely, S., Fazakerley, D. J., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.09.001 · Cited by 426 · see citing works

Acute exercise induces GLUT4 translocation in skeletal muscle of normal human subjects and subjects with type 2 diabetes

Kennedy, J. W., Hirshman, M. F., Gervino, E. V., Ocel, J. V., Forse, R. A., Hoenig, S. J., Aronson, D., Goodyear, L. J., & Horton, E. S. (1999) · Diabetes · doi:10.2337/diabetes.48.5.1192 · Cited by 415 · see citing works

AMP-activated protein kinase (AMPK) β1β2 muscle null mice reveal an essential role for AMPK in maintaining mitochondrial content and glucose uptake during exercise

O'Neill, H. M., Maarbjerg, S. J., Crane, J. D., Jeppesen, J., Jørgensen, S. B., Schertzer, J. D., Shyroka, O., Kiens, B., van Denderen, B. J., Tarnopolsky, M. A., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105062108 · Cited by 406 · see citing works

Ca2+ and AMPK Both Mediate Stimulation of Glucose Transport by Muscle Contractions

Wright, D. C., Hucker, K. A., Holloszy, J. O., & Han, D. H. (2004) · Diabetes · doi:10.2337/diabetes.53.2.330 · Cited by 398 · 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

Skeletal Muscle Glucose Uptake During Exercise: How is it Regulated?

Rose, A. J., & Richter, E. A. (2005) · Physiology · doi:10.1152/physiol.00012.2005 · Cited by 371 · 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

Glucose transport and sensing in the maintenance of glucose homeostasis and metabolic harmony

Herman, M. A. (2006) · Journal of Clinical Investigation · doi:10.1172/jci29027 · Cited by 349 · see citing works

Thirty sweet years of GLUT4

Klip, A., McGraw, T. E., & James, D. E. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.rev119.008351 · Cited by 344 · see citing works

Activation of p38 MAP kinase enhances sensitivity of muscle glucose transport to insulin

Geiger, P. C., Wright, D. C., Han, D., & Holloszy, J. O. (2004) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00477.2004 · Cited by 306 · see citing works

Analysis of GLUT4 Distribution in Whole Skeletal Muscle Fibers: Identification of Distinct Storage Compartments That Are Recruited by Insulin and Muscle Contractions

Ploug, T., van Deurs, B., Ai, H., Cushman, S. W., & Ralston, E. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.6.1429 · Cited by 302 · see citing works

Insulin responsiveness in skeletal muscle is determined by glucose transporter (Glut4) protein level

Kern, M., Wells, J. A., Stephens, J. M., Elton, C. W., Friedman, J. E., Tapscott, E. B., Pekala, P. H., & Dohm, G. L. (1990) · Biochemical Journal · doi:10.1042/bj2700397 · Cited by 267 · see citing works

Divergent response of metabolite transport proteins in human skeletal muscle after sprint interval training and detraining

Burgomaster, K. A., Cermak, N. M., Phillips, S. M., Benton, C. R., Bonen, A., & Gibala, M. J. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00503.2006 · Cited by 255 · see citing works

Physical Training Increases Muscle GLUT4 Protein and mRNA in Patients With NIDDM

Dela, F., Ploug, T., Handberg, A., Petersen, L. N., Larsen, J. J., Mikines, K. J., & Galbo, H. (1994) · Diabetes · doi:10.2337/diab.43.7.862 · Cited by 252 · see citing works

Effect of muscle glycogen depletion on in vivo insulin action in man.

Bogardus, C., Thuillez, P., Ravussin, É., Vasquez, B., Narimiga, M., & Azhar, S. (1983) · Journal of Clinical Investigation · doi:10.1172/jci111119 · Cited by 252 · see citing works

Activation of AMP kinase enhances sensitivity of muscle glucose transport to insulin

Fisher, J. S., Gao, J., Han, D.-H., Holloszy, J. O., & Nolte, L. A. (2002) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2002.282.1.e18 · Cited by 244 · see citing works

Abundance, localization, and insulin-induced translocation of glucose transporters in red and white muscle

Marette, A., Richardson, J. M., Ramlal, T., Balon, T. W., Vranić, M., Pessin, J. E., & Klip, A. (1992) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1992.263.2.c443 · Cited by 242 · see citing works

Cytosolic ROS production by NADPH oxidase 2 regulates muscle glucose uptake during exercise

Henríquez-Olguin, C., Knudsen, J. R., Raun, S. H., Li, Z., Dalbram, E., Treebak, J. T., Sylow, L., Holmdahl, R., Richter, E. A., Jaimovich, E., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12523-9 · Cited by 228 · see citing works

Role of reactive oxygen species in contraction‐mediated glucose transport in mouse skeletal muscle

Sandström, M., Zhang, S., Bruton, J. D., Silva, J., Reid, M. B., Westerblad, H., & Katz, A. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.110601 · Cited by 209 · see citing works

Exercise-stimulated glucose transport in skeletal muscle is nitric oxide dependent

Roberts, C. K., Barnard, R. J., Scheck, S. H., & Balon, T. W. (1997) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1997.273.1.e220 · Cited by 208 · see citing works

Exercise and Myocyte Enhancer Factor 2 Regulation in Human Skeletal Muscle

McGee, S. L., & Hargreaves, M. (2004) · Diabetes · doi:10.2337/diabetes.53.5.1208 · Cited by 205 · see citing works

Effect of endurance training on glucose transport capacity and glucose transporter expression in rat skeletal muscle

Ploug, T., Stallknecht, B. M., Pedersen, O. B., Kahn, B. B., Ohkuwa, T., Vinten, J., & Galbo, H. (1990) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1990.259.6.e778 · Cited by 203 · see citing works

Enhanced Insulin Action Due to Targeted GLUT4 Overexpression Exclusively in Muscle

Tsao, T., Burcelin, R., Katz, E. B., Huang, L., & Charron, M. J. (1996) · Diabetes · doi:10.2337/diab.45.1.28 · Cited by 201 · see citing works

Identification and Characterization of an Exercise-sensitive Pool of Glucose Transporters in Skeletal Muscle

Coderre, L., Kandror, K. V., Vallega, G., & Pilch, P. F. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.46.27584 · Cited by 195 · see citing works

Exercise induces a transient increase in transcription of the GLUT-4 gene in skeletal muscle

Neufer, P. D., & Dohm, G. L. (1993) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1993.265.6.c1597 · Cited by 192 · see citing works

Exercise and insulin cause GLUT-4 translocation in human skeletal muscle

Thorell, A., Hirshman, M. F., Nygren, J., Jorfeldt, L., Wojtaszewski, J. F. P., Dufresne, S. D., Horton, E. S., Ljungqvist, O. H., & Goodyear, L. J. (1999) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1999.277.4.e733 · Cited by 190 · see citing works

Increased GLUT-4 translocation mediates enhanced insulin sensitivity of muscle glucose transport after exercise

Hansen, P. A., Nolte, L. A., Chen, M. M., & Holloszy, J. O. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.85.4.1218 · Cited by 189 · see citing works

Persistent increase in glucose uptake by rat skeletal muscle following exercise

Ivy, J. L., & Holloszy, J. O. (1981) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1981.241.5.c200 · Cited by 185 · see citing works

Exercise training, glucose transporters, and glucose transport in rat skeletal muscles

Rodnick, K. J., Henriksen, E. J., James, D. E., & Holloszy, J. O. (1992) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1992.262.1.c9 · Cited by 183 · see citing works

Immunocytochemical and biochemical studies of GLUT4 in rat skeletal muscle.

Rodnick, K. J., Slot, J. W., Studelska, D. R., Hanpeter, D., Robinson, L. J., Geuze, H. J., & James, D. E. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)42692-0 · Cited by 180 · see citing works

Expression of the Insulin-responsive Glucose Transporter GLUT4 in Adipocytes Is Dependent on Liver X Receptor α

Dalen, K. T., Ulven, S. M., Bamberg, K., Gustafsson, J.-Α., & Nebb, H. I. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302287200 · Cited by 179 · see citing works

Histone Deacetylase 5 Acquires Calcium/Calmodulin-Dependent Kinase II Responsiveness by Oligomerization with Histone Deacetylase 4

Backs, J., Backs, T., Bezprozvannaya, S., McKinsey, T. A., & Olson, E. N. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01611-07 · Cited by 179 · see citing works

Enhanced muscle insulin sensitivity after contraction/exercise is mediated by AMPK

Kjøbsted, R., Munk-Hansen, N., Birk, J. B., Foretz, M., Viollet, B., Björnholm, M., Zierath, J. R., Treebak, J. T., & Wojtaszewski, J. F. P. (2017) · Diabetes · doi:10.2337/db16-0530 · Cited by 178 · see citing works

Nitric oxide synthase inhibition reduces leg glucose uptake but not blood flow during dynamic exercise in humans.

Bradley, S. J., Kingwell, B. A., & McConell, G. K. (1999) · Diabetes · doi:10.2337/diabetes.48.9.1815 · Cited by 171 · see citing works

Overexpression of Glut4 protein in muscle increases basal and insulin-stimulated whole body glucose disposal in conscious mice.

Ren, J., Marshall, B. A., Mueckler, M. M., McCaleb, M. L., Amatruda, J. M., & Shulman, G. I. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117673 · Cited by 171 · see citing works

GLUT 4 and insulin receptor binding and kinase activity in trained human muscle.

Dela, F., Handberg, A., Mikines, K. J., Vinten, J., & Galbo, H. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019833 · Cited by 170 · see citing works

Fiber type-specific expression of GLUT4 in human skeletal muscle: influence of exercise training.

Daugaard, J. R., Nielsen, J., Kristiansen, S., Andersen, J. L., Hargreaves, M., & Richter, E. A. (2000) · Diabetes · doi:10.2337/diabetes.49.7.1092 · Cited by 166 · see citing works

Skeletal Muscle Glucose Transport and Metabolism Are Enhanced in Transgenic Mice Overexpressing the Glut4 Glucose Transporter

Gulve, E. A. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.5.1679 · Cited by 165 · see citing works

Exercise Increases Human Skeletal Muscle Insulin Sensitivity via Coordinated Increases in Microvascular Perfusion and Molecular Signaling

Sjøberg, K. A., Frøsig, C., Kjøbsted, R., Sylow, L., Kleinert, M., Betik, A. C., Shaw, C. S., Kiens, B., Wojtaszewski, J. F. P., Rattigan, S., et al. (2017) · Diabetes · doi:10.2337/db16-1327 · Cited by 164 · see citing works

Effects of exercise on GLUT-4 and glycogenin gene expression in human skeletal muscle

Kraniou, Y. N., Cameron‐Smith, D., Misso, M. L., Collier, G. R., & Hargreaves, M. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.88.2.794 · Cited by 153 · 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

The physiological regulation of glucose flux into musclein vivo

Wasserman, D. H., Kang, L., Ayala, J. E., Fueger, P. T., & Lee, R. S. (2010) · Journal of Experimental Biology · doi:10.1242/jeb.048041 · Cited by 150 · see citing works

Effects of endurance exercise training on muscle glycogen accumulation in humans

Greiwe, J. S., Hickner, R. C., Hansen, P. A., Racette, S. B., Chen, M. M., & Holloszy, J. O. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.1.222 · Cited by 147 · see citing works

Rac1 Is a Novel Regulator of Contraction-Stimulated Glucose Uptake in Skeletal Muscle

Sylow, L., Jensen, T. E., Kleinert, M., Mouatt, J. R., Maarbjerg, S., Jeppesen, J. F., Prats, C., Chiu, T. T., Boguslavsky, S., Klip, A., et al. (2012) · Diabetes · doi:10.2337/db12-0491 · Cited by 143 · see citing works

Exercise training increases GLUT-4 protein concentration in previously sedentary middle-aged men

Houmard, J. A., Shinebarger, M. H., Dolan, P. L., Leggett-Frazier, N., Bruner, R. K., McCammon, M. R., Israel, R. G., & Dohm, G. L. (1993) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1993.264.6.e896 · Cited by 142 · see citing works

Effect of carbohydrate ingestion on glucose kinetics during exercise

McConell, G. K., Fabris, S., Proietto, J., & Hargreaves, M. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.77.3.1537 · Cited by 139 · see citing works

Exercise-induced translocation of skeletal muscle glucose transporters

Goodyear, L. J., Hirshman, M. F., & Horton, E. S. (1991) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1991.261.6.e795 · Cited by 139 · see citing works

Exercise-Induced Increase in Glucose Transporters in Plasma Membranes of Rat Skeletal Muscle*

Douen, A. G., Ramlal, T., Klip, A., YOUNG, D. A., Cartee, G. D., & Holloszy, J. O. (1989) · Endocrinology · doi:10.1210/endo-124-1-449 · Cited by 135 · see citing works

Glucose transporter number, activity, and isoform content in plasma membranes of red and white skeletal muscle

Goodyear, L. J., Hirshman, M. F., Smith, R. J., & Horton, E. S. (1991) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1991.261.5.e556 · Cited by 134 · see citing works

Eccentric exercise decreases glucose transporter GLUT4 protein in human skeletal muscle.

Asp, S., Daugaard, J. R., & Richter, E. A. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020553 · Cited by 132 · see citing works

Glucose Transporter Number, Function, and Subcellular Distribution in Rat Skeletal Muscle After Exercise Training

Goodyear, L. J., Hirshman, M. F., Valyou, P. M., & Horton, E. S. (1992) · Diabetes · doi:10.2337/diab.41.9.1091 · Cited by 130 · see citing works

Effects of muscle activity and fiber composition on glucose transport and GLUT-4

Megeney, L. A., Neufer, P. D., Dohm, G. L., Tan, M. H., Blewett, C., Elder, G. C. B., & Bonen, A. (1993) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1993.264.4.e583 · Cited by 129 · see citing works

Regulation of muscle GLUT4 enhancer factor and myocyte enhancer factor 2 by AMP-activated protein kinase

Holmes, B. F., Sparling, D. P., Olson, A. L., Winder, W. W., & Dohm, G. L. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00606.2004 · Cited by 123 · see citing works

Effects of Exercise Training on Insulin-Regulatable Glucose-Transporter Protein Levels in Rat Skeletal Muscle

Rodnick, K. J., Holloszy, J. O., Mondon, C. E., & James, D. E. (1990) · Diabetes · doi:10.2337/diab.39.11.1425 · Cited by 122 · see citing works

Skeletal muscle glucose uptake during contraction is regulated by nitric oxide and ROS independently of AMPK

Merry, T. L., Steinberg, G. R., Lynch, G. S., & McConell, G. K. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00239.2009 · Cited by 122 · see citing works

Potential role of TBC1D4 in enhanced post-exercise insulin action in human skeletal muscle

Treebak, J. T., Frøsig, C., Pehmøller, C., Chen, S., Maarbjerg, S. J., Brandt, N., MacKintosh, C., Zierath, J. R., Hardie, D. G., Kiens, B., et al. (2009) · Diabetologia · doi:10.1007/s00125-009-1294-y · Cited by 119 · 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

Additive effect of contractions and insulin on GLUT-4 translocation into the sarcolemma

Gao, J., Ren, J., Gulve, E. A., & Holloszy, J. O. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.77.4.1597 · Cited by 116 · cited 1× · see citing works

GLUT4 and Glycogen Synthase Are Key Players in Bed Rest–Induced Insulin Resistance

Biensø, R. S., Ringholm, S., Kiilerich, K., Aachmann‐Andersen, N. J., Krogh‐Madsen, R., Guerra, B., Plomgaard, P., van Hall, G., Treebak, J. T., Saltin, B., et al. (2012) · Diabetes · doi:10.2337/db11-0884 · Cited by 115 · see citing works

CaMK activation during exercise is required for histone hyperacetylation and MEF2A binding at the MEF2 site on the<i>Glut4</i>gene

Smith, J. A. H., Kohn, T. A., Chetty, A. K., & Ojuka, E. O. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00747.2007 · Cited by 115 · see citing works

Rac1 governs exercise‐stimulated glucose uptake in skeletal muscle through regulation of GLUT4 translocation in mice

Sylow, L., Nielsen, I. L., Kleinert, M., Møller, L. L. V., Ploug, T., Schjerling, P., Bilan, P. J., Klip, A., Jensen, T. E., & Richter, E. A. (2016) · The Journal of Physiology · doi:10.1113/jp272039 · Cited by 114 · see citing works

Acute exercise increases the number of plasma membrane glucose transporters in rat skeletal muscle

Hirshman, M. F., Wallberg‐Henriksson, H., Wardzala, L. J., Horton, E. D., & Horton, E. S. (1988) · FEBS Letters · doi:10.1016/0014-5793(88)80486-1 · Cited by 113 · see citing works

Changes in insulin action and GLUT-4 with 6 days of inactivity in endurance runners

Vukovich, M. D., Arciero, P. J., Kohrt, W. M., Racette, S. B., Hansen, P. A., & Holloszy, J. O. (1996) · Journal of Applied Physiology · doi:10.1152/jappl.1996.80.1.240 · Cited by 110 · see citing works

Glucose uptake and transport in contracting, perfused rat muscle with different pre‐contraction glycogen concentrations.

Hespel, P., & Richter, E. A. (1990) · The Journal of Physiology · doi:10.1113/jphysiol.1990.sp018175 · Cited by 108 · see citing works

Regulation of the human GLUT4 gene promoter: Interaction between a transcriptional activator and myocyte enhancer factor 2A

Knight, J. B., Eyster, C. A., Griesel, B. A., & Olson, A. L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2432756100 · Cited by 108 · see citing works

Improved insulin action in muscle, liver, and adipose tissue in physically trained human subjects

Rodnick, K. J., Haskell, W. L., Swislocki, A., Foley, J. E., & Reaven, G. M. (1987) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1987.253.5.e489 · Cited by 107 · see citing works

Skeletal muscle overexpression of nuclear respiratory factor 1 increases glucose transport capacity

Baar, K., Song, Z., Semenkovich, C. F., Jones, T. E., Han, D.-H., Nolte, L. A., Ojuka, E. O., Chen, M. W., & Holloszy, J. O. (2003) · The FASEB Journal · doi:10.1096/fj.03-0049com · Cited by 106 · see citing works

Muscle glycogen accumulation after endurance exercise in trained and untrained individuals

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Human skeletal muscle fiber type-specific responses to sprint interval and moderate-intensity continuous exercise: acute and training-induced changes

Skelly, L. E., Gillen, J. B., Frankish, B. P., MacInnis, M. J., Godkin, F. E., Tarnopolsky, M. A., Murphy, R. M., & Gibala, M. J. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00862.2020 · Cited by 38 · see citing works

Exercise as a tool to mitigate metabolic disease

Esteves, J. V. D. C., & Stanford, K. I. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00144.2024 · Cited by 38 · see citing works

Extracellular vesicles in metabolic perspective: mechanism and targeted therapy

Sheng, Q., Wu, Z., Li, W., Wang, L., Xu, H., Wang, W., Yan, Z., Ge, G., Xu, Y., & Geng, D. (2025) · Journal of Nanobiotechnology · doi:10.1186/s12951-025-03763-7 · Cited by 35 · see citing works

The Role of Natural Antioxidant Products That Optimize Redox Status in the Prevention and Management of Type 2 Diabetes

Tuell, D. S., LOS, E. A., Ford, G. A., & Stone, W. L. (2023) · Antioxidants · doi:10.3390/antiox12061139 · Cited by 34 · see citing works

Metabolo-epigenetic interplay provides targeted nutritional interventions in chronic diseases and ageing

de Cedrón, M. G., Palomares, R. M., & de Molina, A. R. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1169168 · Cited by 31 · see citing works

Feeding Tolerance, Glucose Availability, and Whole-Body Total Carbohydrate and Fat Oxidation in Male Endurance and Ultra-Endurance Runners in Response to Prolonged Exercise, Consuming a Habitual Mixed Macronutrient Diet and Carbohydrate Feeding During Exercise

Rauch, C., McCubbin, A. J., Gaskell, S. K., & Costa, R. J. S. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2021.773054 · Cited by 29 · see citing works

Impact of Physical Activity on Cellular Metabolism Across Both Neurodegenerative and General Neurological Conditions: A Narrative Review

Clemente‐Suárez, V. J., Rubio-Zarapuz, A., Belinchón-deMiguel, P., Beltrán-Velasco, A. I., Martín-Rodríguez, A., & Tornero-Aguilera, J. F. (2024) · Cells · doi:10.3390/cells13231940 · Cited by 30 · see citing works

Exercise and health: historical perspectives and new insights

Hargreaves, M. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00242.2021 · Cited by 25 · see citing works

Potential Mechanisms for How Long-Term Physical Activity May Reduce Insulin Resistance

Lee-Ødegård, S., Olsén, T., Norheim, F., Drevon, C. A., & Birkeland, K. I. (2022) · Metabolites · doi:10.3390/metabo12030208 · Cited by 20 · see citing works

Critical Review on Anti-Obesity Effects of Anthocyanins Through PI3K/Akt Signaling Pathways

Randeni, N., Luo, J., & Xu, B. (2025) · Nutrients · doi:10.3390/nu17071126 · Cited by 20 · see citing works

Impact of pre‐exercise feeding status on metabolic adaptations to endurance‐type exercise training

Edinburgh, R. M., Koumanov, F., & Gonzalez, J. T. (2021) · The Journal of Physiology · doi:10.1113/jp280748 · Cited by 20 · see citing works

Impact of cancer cachexia on respiratory muscle function and the therapeutic potential of exercise

Murphy, B. T., Mackrill, J. J., & O’Halloran, K. D. (2022) · The Journal of Physiology · doi:10.1113/jp283569 · Cited by 20 · see citing works

Integrated analysis of Solute carrier family-2 members reveals SLC2A4 as an independent favorable prognostic biomarker for breast cancer

Shi, Z., Liu, J., Wang, F., & Li, Y. (2021) · Channels · doi:10.1080/19336950.2021.1973788 · Cited by 17 · see citing works

Regulation of nutrient uptake by AMP-activated protein kinase

Alghamdi, F. B., Alshuweishi, Y., & Salt, I. P. (2020) · Cellular Signalling · doi:10.1016/j.cellsig.2020.109807 · Cited by 17 · see citing works

O-GlcNAcylation: The Underestimated Emerging Regulators of Skeletal Muscle Physiology

Liu, Y., Hu, Y., Fan, W.-X., Quan, X., Xu, B., & Li, S. (2022) · Cells · doi:10.3390/cells11111789 · Cited by 15 · see citing works

The activation of AMPK/PGC-1α/GLUT4 signaling pathway through early exercise improves mitochondrial function and mitigates ischemic brain damage

Wu, X., Li, C., Ke, C., Huang, C., Pan, B., & Wan, C. (2024) · Neuroreport · doi:10.1097/wnr.0000000000002048 · Cited by 15 · see citing works

G6PD Deficiency Is Crucial for Insulin Signaling Activation in Skeletal Muscle

Jiang, A., Guo, H., Jiang, X., Tao, J., Wu, W., & Liu, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137425 · Cited by 14 · see citing works

Type 2 Diabetes Mellitus as a Multisystem Disease: From Insulin Resistance to Organ Crosstalk—A Narrative Review

Fuentes-Barría, H., Aguilera-Eguía, R. A., Flores-Fernández, C., Angarita, L., & Alarcón-Rivera, M. (2026) · Biomedicines · doi:10.3390/biomedicines14040752 · Cited by 18 · see citing works

Novel Expression of GLUT3, GLUT6 and GLUT10 in Equine Gluteal Muscle Following Glycogen-Depleting Exercise: Impact of Dietary Starch and Fat

Valberg, S. J., Velez‐Irizarry, D., Williams, Z. J., Pagan, J. D., de Mesquita, V. S., Waldridge, B. M., & Maresca-Fichter, H. C. (2023) · Metabolites · doi:10.3390/metabo13060718 · Cited by 12 · see citing works

Complementary Approaches to Retinal Health Focusing on Diabetic Retinopathy

Rák, T., Kovács-Valasek, A., Pöstyéni, E., Csutak, A., & Gabriel, R. (2023) · Cells · doi:10.3390/cells12232699 · Cited by 13 · see citing works

Improved Aerobic Capacity and Adipokine Profile Together with Weight Loss Improve Glycemic Control without Changes in Skeletal Muscle GLUT-4 Gene Expression in Middle-Aged Subjects with Impaired Glucose Tolerance

Venojärvi, M., Lindström, J., Aunola, S., Nuutila, P., & Atalay, M. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19148327 · Cited by 12 · see citing works

Dietary tea seed saponin combined with aerobic exercise attenuated lipid metabolism and oxidative stress in mice fed a high‐fat diet (HFD)

Cao, W., Wang, K., Liang, C., Su, Y., Liu, S., Li, J., Qing, H., Zeng, Z., Dai, L., & Song, J. (2022) · Journal of Food Biochemistry · doi:10.1111/jfbc.14461 · Cited by 12 · see citing works

Exercise-related alterations in MCT1 and GLUT4 expressions in the liver and pancreas of rats with STZ-induced diabetes

Amirkhosravi, L., Kordestani, Z., Nikooei, R., Safi, Z., Yeganeh‐Hajahmadi, M., & Goki, M. M. (2023) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-023-01255-9 · Cited by 13 · see citing works

Muscle-Specific Ablation of Glucose Transporter 1 (GLUT1) Does Not Impair Basal or Overload-Stimulated Skeletal Muscle Glucose Uptake

McMillin, S. L., Evans, P. L., Taylor, W. M., Weyrauch, L. A., Sermersheim, T. J., Welc, S. S., Heitmeier, M. R., Hresko, R. C., Hruz, P. W., Koumanov, F., et al. (2022) · Biomolecules · doi:10.3390/biom12121734 · Cited by 11 · see citing works

ArfGAP3 regulates vesicle transport and glucose uptake in myoblasts

Li, S., Wang, Z., Chen, M., Xiao, Y., Min, J., Hu, M., Tang, J., & Li, H. (2022) · Cellular Signalling · doi:10.1016/j.cellsig.2022.110551 · Cited by 11 · see citing works

Effect of eight weeks of vitamin D supplementation and water-based exercise on cardiometabolic profile in women with type 2 diabetes

Salarinia, M., Azizi, M., Tahmasebi, W., & Khalvandi, H. (2023) · Science & Sports · doi:10.1016/j.scispo.2022.04.008 · Cited by 10 · see citing works

miR-153-3p via PIK3R1 Is Involved in Cigarette Smoke-Induced Neurotoxicity in the Brain

Sun, Q., Wang, H., Yang, M., Xia, H., Wu, Y., Liu, Q., & Tang, H. (2023) · Toxics · doi:10.3390/toxics11120969 · Cited by 10 · see citing works

Enhanced skeletal muscle glycogen repletion after endurance exercise is associated with higher plasma insulin and skeletal muscle hexokinase 2 protein levels in mice: comparison of level running and downhill running model

Takahashi, Y., Sarkar, J., Yamada, J., Matsunaga, Y., Nonaka, Y., Banjo, M., Sakaguchi, R., Shinya, T., & Hatta, H. (2021) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-021-00806-z · Cited by 10 · see citing works

The combination of cardiorespiratory fitness and muscular fitness, and prevalence of diabetes mellitus in middle-aged and older men: WASEDA’S Health Study

Wang, D., Sawada, S. S., Tabata, H., Kawakami, R., Ito, T., Tanisawa, K., Higuchi, M., Ishii, K., Oka, K., Suzuki, K., et al. (2022) · BMC Public Health · doi:10.1186/s12889-022-12971-x · Cited by 9 · see citing works

Different Fasting Methods Combined With Running Exercise Regulate Glucose Metabolism via AMPK / SIRT1 / BDNF Pathway in Mice

Wang, X., Shi, J., Li, Y., Zhou, L., Xu, L., Wang, J., Liu, C., & Liang, B. (2025) · Comprehensive physiology · doi:10.1002/cph4.70031 · Cited by 8 · see citing works

Skeletal Muscle Hyperemia: A Potential Bridge Between Post-exercise Hypotension and Glucose Regulation

Pellinger, T. K., & Emhoff, C. W. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2021.821919 · Cited by 8 · see citing works

Exploring the Molecular Adaptations, Benefits, and Future Direction of Exercise Training: Updated Insights into Cardiovascular Health

Mendoza, M. F., Suan, N. M., & Lavie, C. J. (2024) · Journal of Functional Morphology and Kinesiology · doi:10.3390/jfmk9030131 · Cited by 7 · see citing works

Effects of concurrent aerobic and strength training in patients with type 2 diabetes: Bayesian pairwise and dose-response meta-analysis

Han, X., Zou, Y., & Zhang, S. (2024) · BMJ Open Diabetes Research & Care · doi:10.1136/bmjdrc-2024-004400 · Cited by 7 · see citing works

Health benefits of physical activity: What role does skeletal muscle-organ crosstalk play?

Powers, S. K., Goldstein, E. R., Lategan-Potgieter, R., Schrager, M. A., Skelton, M., & Demirel, H. A. (2025) · Sports Medicine and Health Science · doi:10.1016/j.smhs.2025.02.010 · Cited by 7 · see citing works

Exercise‐induced signalling in alleviating neuronal insulin resistance

Reddy, I., & Dey, C. S. (2025) · The Journal of Physiology · doi:10.1113/jp287750 · Cited by 7 · see citing works

Effect of an acute long-duration exercise bout on skeletal muscle lipid droplet morphology, GLUT 4 protein, and perilipin protein expression

Bajpeyi, S., Apaflo, J. N., Rosas, V., Sepulveda-Rivera, K., Varela-Ramı́rez, A., Covington, J. D., Galgani, J. E., & Ravussin, É. (2023) · European Journal of Applied Physiology · doi:10.1007/s00421-023-05266-5 · Cited by 7 · see citing works

Myokine IL-6 activity enhances post-exercise fatty acid accumulation in skeletal muscle but does not affect glycogen resynthesis

Kistner, T. M., Trinh, B., Mfeketo, K., van Hall, G., Pedersen, B. K., Lieberman, D. E., & Ellingsgaard, H. (2025) · Molecular Metabolism · doi:10.1016/j.molmet.2025.102283 · Cited by 7 · see citing works

Canonical and Alternative Pathways (Insulin and Exercise) of GLUT4 Synthesis, Signaling, Intracellular Clustering, and Recruitment to the Plasma Membrane

Ramos‐Jiménez, A., Rubio-Valles, M., Arvizuo, J. G., Juárez-Oropeza, M. A., Ramos-Hernández, J. A., Chávez-Guevara, I. A., González-Rodríguez, E., Moreno-Brito, V., & Torres, R. P. H. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27083475 · Cited by 6 · see citing works

Vitamin D3 supplementation could improve the effect of exercise training on type 2 diabetes-induced metabolic disorders via BDNF/irisin axis in elderly women

Mashhadi, M. R., Bijeh, N., Rashidlamir, A., & Raoof, A. A. (2024) · Sport Sciences for Health · doi:10.1007/s11332-024-01204-w · Cited by 5 · see citing works

The link of environmental estrogens exposure to oxidative stress and their association with insulin- and exercise-induced glucose uptake

Riffee, J. N. J., Wade, M., Sine, T., Griffith, C., Benite‐Ribeiro, S. A., Haney, A. C., & dos Santos, J. M. (2023) · Obesity Medicine · doi:10.1016/j.obmed.2023.100503 · Cited by 4 · see citing works

Resistance training and cardiovascular health: epigenetic regulation

Silva, J. G., Rodrigues, L. F., Torres, T., Caria, A. C. I., Oliveira, E. M., & Fernandes, T. M. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2025.1701689 · Cited by 3 · see citing works

Physical exercise induces increased translocation of type 4 glucose transporters (GLUT4): a systematic review

Ayubi, N., Wibawa, J. C., Lesmana, H. S., Callixte, C., & Dafun, P. B. (2024) · Retos · doi:10.47197/retos.v59.104078 · Cited by 3 · see citing works

Vitamin D and exercise in obesity: a neurovascular–muscle axis

Zheng, X., & Zhang, C. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1750915 · Cited by 3 · see citing works

Body mass conversion and improved insulin response in Colombian Paso horses subjected to a swimming training program

Cabrera, A. M. Z., Pineda, W. R. R., Correa‐Valencia, N. M., & Gutiérrez, M. P. A. (2022) · Comparative Exercise Physiology · doi:10.3920/cep210024 · Cited by 3 · see citing works

Dynamics of training and acute exercise-induced shifts in muscular glucose transporter (GLUT) 4, 8, and 12 expression in locomotion versus posture muscles in healthy horses

de Vega, C. V. M., Lemmens, D., meeûs, C. D., Boshuizen, B., Maré, L. D., Leybaert, L., Goethals, K., de Oliveira, J. E., Hosotani, G., Deforce, D. L. D., et al. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1256217 · Cited by 3 · see citing works

Moderate Effects of Hypoxic Training at Low and Supramaximal Intensities on Skeletal Muscle Metabolic Gene Expression in Mice

Drozdovska, S., Zanou, N., Lavier, J., Mazzolai, L., Millet, G. P., & Pellegrin, M. (2023) · Metabolites · doi:10.3390/metabo13101103 · Cited by 4 · see citing works

Machine Learning Reveals Microbial Taxa Associated with a Swim across the Pacific Ocean

Lewis, G. S., Reczek, S., Omozusi, O., Hogue, T., Cook, M. D., & Hampton-Marcell, J. (2023) · Biomedicines · doi:10.3390/biomedicines12102309 · Cited by 3 · see citing works

A Single Intraperitoneal Secreted Protein Acidic and Rich in Cysteine Injection in Mice Is Towards an Exercise-like Phenotype

Ghanemi, A., Yoshioka, M., & St‐Amand, J. (2025) · Biology · doi:10.3390/biology14040398 · Cited by 2 · see citing works

Special Issue “Skeletal Muscle Adaptations to Oxidative Stress”

Duranti, G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199809 · Cited by 2 · see citing works

Optimising exercise time-of-day for cardiometabolic health: Insights from a systematic review and meta-analysis in varied adult cohorts

Fitzpatrick, R., Wilson, J. J., Davison, G. W., McMahon, G. E., Bleakley, C., & McClean, C. M. (2026) · Journal of Sports Sciences · doi:10.1080/02640414.2026.2637042 · Cited by 3 · see citing works

Early introduction of exercise prevents insulin resistance in postnatal overfed rats

Fischer, S. V., Appel, M. H., Naliwaiko, K., Pagliosa, D. D., Araújo, D. N., Capote, A. E., Oliveira, B. A. C., & Fernandes, L. C. (2022) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x2022e11987 · Cited by 2 · see citing works

Moderate intensity continuous and interval training affect visceral fat and insulin resistance model in female rat exposed high calorie diet

Riyono, A., Tinduh, D., Othman, Z., & Herawati, L. (2022) · Comparative Exercise Physiology · doi:10.3920/cep220013 · Cited by 2 · see citing works

Exercise Prescription Principles among Physicians and Physical Therapists for Patients with Impaired Glucose Control: A Cross-Sectional Study

Petrie, M. A., Johnson, K. A., Dubey, O., & Shields, R. K. (2023) · Journal of Functional Morphology and Kinesiology · doi:10.3390/jfmk8030112 · Cited by 2 · see citing works

Metabolic Consequences of Polycystic Ovary Syndrome and Their Impact on Hepatic Function in High Fat Diet-Fed Rats: Potential Role of Moderate Intensity Exercise

Hamed, G. M., Abou-Bakr, D. A., Saleh, N., Elshishiny, M. I., & Morsy, W. E. (2024) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093024040124 · Cited by 2 · see citing works

Enhanced Oxygen Utilization Efficiency With Concomitant Activation of AMPK-TBC1D1 Signaling Nexus in Cyclophilin-D Conditional Knockout Mice

Radhakrishnan, J., Baetiong, A., & Gazmuri, R. J. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.756659 · Cited by 2 · see citing works

Effect of High-intensity Interval Training with Royal Jelly Consumption on Serum Levels of Glucose, Insulin, and Insulin Resistance Index of Overweight and Obese Middle-aged Men: A Quasi-experimental Study

Gohari, I., Khajehlandi, A., & Mohammadi, A. (2022) · Jundishapur Journal of Chronic Disease Care · doi:10.5812/jjcdc-123363 · Cited by 2 · see citing works

ATPase Inhibitory Factor 1—A Novel Marker of Cellular Fitness and Exercise Capacity?

Domin, R., Pytka, M., Niziński, J., Żołyński, M., Zybek‐Kocik, A., Wrotkowska, E., Zieliński, J., Guzik, P., & Ruchała, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315303 · Cited by 2 · see citing works

Effects of insect consumption on exercise performance, body composition and metabolism: a review

Vanlin, J., Selvanayagam, V. S., Khong, T. K., & Yusof, A. (2024) · Journal of Insects as Food and Feed · doi:10.1163/23524588-00001104 · Cited by 1 · see citing works

A Rare Case of Small Bowel Ulceration Induced by COVID-19

Gao, X., Shi, L., Jing, D., Ma, C., Wang, Q., Wang, J., Zhu, F., Zhao, M., Chen, Y., & Zhou, G. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s507209 · Cited by 1 · see citing works

Design of debunking the frailty–sarcopenia–ADT axis in metastatic prostate cancer with multicomponent exercise: the FIERCE trial protocol

Wilson, R. L., Vulczak, A., Morgans, A. K., Norris, M. K., Greer, J., VOTTA, J. L., Vamvini, M. T., Einstein, D. J., Uno, H., Rosenthal, M. H., et al. (2025) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2025.1602123 · Cited by 1 · see citing works

Phenolic acids in brown rice attenuate postprandial inflammation in sedentary office workers: mechanisms and implications

Putri, R. F., Jusman, S. W. A., & Lestari, W. (2025) · Precision Nutrition · doi:10.1097/pn9.0000000000000125 · Cited by 1 · see citing works

The metabolic implications of maternal exercise: effects on pregnant women and their offspring

He, Z., Yuan, Y., Zhang, L. Y., Niu, W., Liu, L., Chen, B., & Wang, X. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1741714 · Cited by 1 · see citing works

Examining the impact of GLUT4 protein molecular mechanism on skeletal muscle exercise metabolism through electrochemical sensors: Role of protein macromolecules

Luo, S., & Xie, J. (2026) · Microchemical Journal · doi:10.1016/j.microc.2026.118000 · Cited by 1 · see citing works

Resistance training and diabetes mellitus type 2: An umbrella review of systematic reviews and meta-analyses on glycemic and cardiometabolic outcomes

Trybulski, R., Żebrowska, A., Fostiak, K., Olaniszyn, G., & Wilk, M. (2026) · Metabolism · doi:10.1016/j.metabol.2026.156671 · Cited by 1 · see citing works

Heat Shock Proteins and Exercise in Skeletal Muscle Insulin Resistance: Protective Mechanisms and Therapeutic Potential

Othman, M., Kim, J. H., Kamal, K. Y., & Lawler, J. M. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27156587 · Cited by 1 · see citing works

Exercise as a Molecular Therapeutic Strategy in Metabolic Syndrome: Integrating Cellular Signaling, Organ Crosstalk, and Clinical Translation—A Narrative Review

Fuentes-Barría, H., Aguilera-Eguía, R. A., Alarcón-Rivera, M., & Flores-Fernández, C. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48080850 · Cited by 1 · see citing works

Overview of Exercise Metabolism

Hargreaves, M. (2022) · Physiology in health and disease · doi:10.1007/978-3-030-94305-9_2 · Cited by 1 · see citing works

Diabetes, Aging, and Insulin’s Reponic Features: Review

Moen, J. (2022) · Current Diabetes Reviews · doi:10.2174/1573399819666221031140713 · Cited by 1 · see citing works

Modified-release gliclazide acutely improves recovery but causes undesirable blood glucose decrease after a resistance exercise session in healthy adults: a pilot study for a randomized clinical trial

Martins, J. B., Zanella, D., Nunes, R. B., Collado, P. S., & Lehnen, A. M. (2024) · Archives of Endocrinology and Metabolism · doi:10.20945/2359-4292-2023-0381 · Cited by 1 · see citing works

The Effect of Pyramid Aerobic Training and Karela Herbal Supplement on Glycemic Control in Patients with Type 2 Diabetes

Ghalavand, A., Kardan, H., Nasiri, M., Delaramnasab, M., Masjedi, H., Ghobadi, M. R., & Hosseini, A. (2022) · International journal of basic science in medicine · doi:10.34172/ijbsm.2022.23 · Cited by 1 · see citing works

Changes in Serum Levels of Retinol Binding Protein 4, Glucose and Insulin in Adaptation to Nettle Supplementation and Combination Training in Overweight Men With Type 2 Diabetes

Taeid, V., lorestani, A. Z., Ghaderi, M., Gharani, H., Mehdizadeh, Y., & Havasi, M. (2021) · مجله علمی پزشکی جندی شاپور · doi:10.32598/jsmj.20.3.2416

The effect of environmental estrogens exposure on oxidative stress and dyslipidemia, and their impact on insulin sensitivityPreprint

Riffee, J. N. J., Wade, M., Sine, T., Griffith, C., Benite‐Ribeiro, S. A., Haney, A. C., & dos Santos, J. M. (2022) · Research Square · doi:10.21203/rs.3.rs-2176193/v1

Can poor sleep, body fat mass, and low physical activity contribute mutually to an increase in childhood obesity?

da Silva, A. L. A., Vieira, E. C., Ritter, W. R. G., Rauber, S. B., Lewis, J. E., & Campbell, C. S. G. (2023) · Brazilian Journal of Health Review · doi:10.34119/bjhrv6n3-224

Evidence and Implementation of Physical Activity and Exercise in Diabetes Mellitus

Jáuregui-Ulloa, E. E., Lopez-Taylor, J. R., Soria-Rodriguez, R. A., & García-Camarena, R. (2023) · Springer eBooks · doi:10.1007/978-3-031-25519-9_33

Integrative Transcriptomic Profiling and WGCNA Reveals Key Genetic Determinants of StrabismusPreprint

Li, F., Long, D., Guo, H., Luo, F., Deng, S., Li, Y., & He, H. J. (2024) · Research Square · doi:10.21203/rs.3.rs-4290347/v1

Association between Metabolic flexibility and Hepatic fat content in individuals with Non- alcoholic fatty liver diseasePreprint

Huang, W., He, Y., Ruan, W., Zhai, H., Lin, Y., Dai, X., Wang, T., Huo, C., Zhuang, J., & Jin, L. (2024) · Research Square · doi:10.21203/rs.3.rs-4336762/v1

Gliclazide enhances exercise performance and recovery of muscle strength in healthy trained individuals: a randomized controlled trialPreprint

Martins, J. B., Dipp, T., Schaan, B. D., & Lehnen, A. M. (2024) · Research Square · doi:10.21203/rs.3.rs-4450743/v1

Energy Metabolism: Responses to Exercise and Training

Geor, R. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-7020-8370-9.00040-0

The Complexities of Metabolic Flexibility and Precision Approaches to Sustainable Weight Management

Theodorakis, N., Kreouzi, M., Pappas, A., Feretzakis, G., Sakagianni, A., Kalodanis, K., Αναστασίου, Α., Nikolaou, M., & Koumpouros, Y. (2025) · IGI Global eBooks · doi:10.4018/979-8-3693-5787-3.ch005

Glucose Transporters

Hargreaves, M. (2025) · Springer eBooks · doi:10.1007/978-3-032-05988-8_90

Behavioral and dietary factors in U.S. early childhood type II diabetes

Dunn, A. L., Brinzo, P., Kaleem, S., Lent, A., Etzel, M., Mendonca, J., Jhumkhawala, V., Khoury, M., & Sacca, L. (2025) · Pediatric Research · doi:10.1038/s41390-025-04417-y

Study on the anti fatigue activity and mechanism of GLUT4 protein macromolecule in exercise using electrochemical sensors: changes in RNA and protein expression

Dan, M., & Ji, Y. (2025) · Microchemical Journal · doi:10.1016/j.microc.2025.115815

Muscle Energetics and Fatigue

Feher, J. J. (2025) · Elsevier eBooks · doi:10.1016/b978-0-12-820476-4.00027-8

Physiological Mechanisms of Acute Resistance Training in Reducing Blood Glucose Levels in Women with a Sedentary Lifestyle: A Randomized Controlled Trial

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Additional file 1 of The combination of cardiorespiratory fitness and muscular fitness, and prevalence of diabetes mellitus in middle-aged and older men: WASEDA’S Health Study

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