Heterogeneity of pig intestinal d-glucose transport systems

Statistical Methods

Snedecor, G. W., Cochran, W. G., & STOUT, B. B. (1939) · Soil Science · doi:10.1097/00010694-193902000-00006 · Cited by 19,423 · see citing works

Handbook of Physiology.

Plum, F. (1960) · Archives of Neurology · doi:10.1001/archneur.1960.03840090124020 · Cited by 10,388 · see citing works

Fructose transporter in human spermatozoa and small intestine is GLUT5.

Burant, C., Takeda, J., Brot‐Laroche, E., Bell, G. I., & Davidson, N. O. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)42067-4 · Cited by 545 · see citing works

Molecular physiology of sodium-glucose cotransporters.

Hediger, M. A., & Rhoads, D. B. (1994) · Physiological Reviews · doi:10.1152/physrev.1994.74.4.993 · Cited by 417 · see citing works

Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogene-like sequence (GLUT6).

Kayano, T., Burant, C., Fukumoto, H., Gould, G. W., Fan, Y. S., Eddy, R. L., Byers, M. G., Shows, T. B., Seino, S., & Bell, G. I. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38295-x · Cited by 389 · see citing works

Multiple transport pathways for neutral amino acids in rabbit jejunal brush border vesicles

Stevens, B. R., Ross, H. J., & Wright, E. M. (1982) · The Journal of Membrane Biology · doi:10.1007/bf01868496 · Cited by 303 · see citing works

Expression of human glucose transporters in Xenopus oocytes: kinetic characterization and substrate specificities of the erythrocyte, liver, and brain isoforms

Gould, G. W., THOMAS, H. M., Jess, T. J., & Bell, G. I. (1991) · Biochemistry · doi:10.1021/bi00235a004 · Cited by 303 · see citing works

Rabbit small intestinal brush border membrane. Preparation and lipid composition

Hauser, H., Howell, K. E., DAWSON, R. M. C., & Bowyer, D. E. (1980) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(80)90335-1 · Cited by 283 · see citing works

The Intestinal Na+/Glucose Cotransporter

Wright, E. M. (1993) · Annual Review of Physiology · doi:10.1146/annurev.ph.55.030193.003043 · Cited by 221 · see citing works

GLUT2 is the transporter for fructose across the rat intestinal basolateral membrane

Cheeseman, C. I. (1993) · Gastroenterology · doi:10.1016/0016-5085(93)90948-c · Cited by 155 · see citing works

Transport of Sugars and Amino Acids in the Intestine: Evidence for a Common Carrier

Alvarado, F. (1966) · Science · doi:10.1126/science.151.3713.1010 · Cited by 138 · see citing works

Analysis of kinetic data in transport studies: New insights from kinetic studies of Na+-d-glucose cotransport in human intestinal brush-border membrane vesicles using a fast sampling, rapid filtration apparatus

Malo, C., & Berteloot, A. (1991) · The Journal of Membrane Biology · doi:10.1007/bf01872636 · Cited by 129 · see citing works

Facilitated Glucose Transporters in Epithelial Cells

Thorens, B. (1993) · Annual Review of Physiology · doi:10.1146/annurev.ph.55.030193.003111 · Cited by 127 · see citing works

Sarcoplasmic reticulum Ca2+ content, L‐type Ca2+ current and the Ca2+ transient in rat myocytes during β‐adrenergic Stimulation

Hussain, M., & Orchard, C. H. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.385bb.x · Cited by 117 · see citing works

Kinetics of sodiumd-glucose cotransport in bovine intestinal brush border vesicles

Kaunitz, J. D., & Wright, E. M. (1984) · The Journal of Membrane Biology · doi:10.1007/bf01868525 · Cited by 100 · see citing works

Temperature sensitivity and substrate specificity of two distinct Na+-activated D-glucose transport systems in guinea pig jejunal brush border membrane vesicles.

Brot‐Laroche, E., Serrano, M. A., Delhomme, B., & Alvarado, F. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)84544-1 · Cited by 73 · see citing works

Age-related changes in sodium-dependent glucose transport in rat small intestine

Freeman, H. J., & Quamme, G. A. (1986) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1986.251.2.g208 · Cited by 38 · see citing works

Independent modulation by food supply of two distinct sodium-activated D-glucose transport systems in the guinea pig jejunal brush-border membrane.

Brot‐Laroche, E., Dao, M. T., Alcalde, A. I., Delhomme, B., Triadou, N., & Alvarado, F. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.17.6370 · Cited by 36 · see citing works

D-glucose and L-leucine transport by human intestinal brush-border membrane vesicles

Harig, J. M., Barry, J. A., Rajendran, V., Soergel, K. H., & Ramaswamy, K. (1989) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1989.256.3.g618 · Cited by 34 · see citing works

Salivary, gastric, pancreatic, and hepatobiliary secretion

Forte, J. G., & Rauner, B. B. (1989) · American Physiological Society eBooks · Cited by 33 · see citing works

Disaccharide uptake by brush-border membrane vesicles lacking the corresponding hydrolases

Brot‐Laroche, E., & Alvarado, F. (1984) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(84)90168-8 · Cited by 31 · see citing works

D-Glucose transport in piglet jejunal brush-border membranes: insights from a disease model

Keljo, D. J., Macleod, J., Perdue, M. H., Butler, D. G., & Hamilton, J. R. (1985) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1985.249.6.g751 · Cited by 28 · see citing works

Characterization of the d-glucose/Na+ cotransport system in the intestinal brush-border membrane by using the specific substrate, methyl α-d-glucopyranoside

Brot‐Laroche, E., Supplisson, S., Delhomme, B., Alcalde, A. I., & Alvarado, F. (1987) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(87)90088-5 · Cited by 24 · see citing works

Mechanisms of Sugar Transport Across the Intestinal Brush Border Membrane

Brot‐Laroche, E., & Alvarado, F. (1983) · Proceedings in life sciences · doi:10.1007/978-3-642-69109-6_11 · Cited by 22 · see citing works

Allosterism and Na++-d-glucose cotransport kinetics in rabbit jejunal vesicles: Compatibility with mixed positive and negative cooperativities in a homo- dimeric or tetrameric structure and experimental evidence for only one transport protein involved

Chenu, C., & Berteloot, A. (1993) · The Journal of Membrane Biology · doi:10.1007/bf00239000 · Cited by 21 · see citing works

Kinetic evidence for separate systems in transport of D- and L-methionine by rat small intestine

Brachet, P., Alvarado, F., & PUIGSERVER, A. J. (1987) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1987.252.3.g320 · Cited by 20 · see citing works

A systematic approach to the analysis of intestinal transport kinetics.

van Melle, G., & Jw, R. (1981) · PubMed · Cited by 20 · see citing works

Kinetics of d-glucose transport across the intestinal brush-border membrane of the cat

Wolffram, S., Eggenberger, E., & Scharrer, E. (1989) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(89)90793-7 · Cited by 19 · see citing works

Single‐site uptake of neutral amino acids into guinea‐pig intestinal rings.

Robinson, J. W. L., & van Melle, G. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014092 · Cited by 18 · see citing works

Phenylalanine transport in guinea pig jejunum. A general mechanism for organic solute and sodium cotransport.

Alvarado, F., & Lherminier, M. (1982) · PubMed · Cited by 13 · see citing works

Alkali-metal-ion- and H+-dependent activation and/or inhibition of intestinal brush-border sucrase. A model involving three functionally distinct key prototropic groups

Vasseur, M., van Melle, G., Frangne, R., & Alvarado, F. (1988) · Biochemical Journal · doi:10.1042/bj2510667 · Cited by 11 · see citing works

Kinetic characterization of Na+/d-mannose cotransport in dog kidney: comparison with Na+/d-glucose cotransport

Silverman, M. R., & Ho, L. L. (1993) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(93)90273-3 · Cited by 11 · see citing works

Trans-potassium effects on the chloride/proton symporter activity of guinea-pig ileal brush-border membrane vesicles

Vasseur, M., Caüzac, M., Frangne, R., & Alvarado, F. (1992) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(92)90341-i · Cited by 9 · see citing works

Ontogeny of Na+/D-glucose cotransport in guinea-pig jejunal vesicles: only one system is involved at both 20°C and 35°C

Malo, C. (1993) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(93)90419-z · Cited by 8 · see citing works

Effect of chronic cold exposure on Na-dependent D-glucose transport along small intestine in ducklings

Thomas, V., Pichon, B., Crouzoulon, G., & Barré, H. (1996) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1996.271.5.r1429 · Cited by 5 · see citing works

pH gradient effects on chloride transport across basolateral membrane vesicles from guinea‐pig jejunum.

Touzani, K., Alvarado, F., & Vasseur, M. (1997) · The Journal of Physiology · doi:10.1113/jphysiol.1997.sp022029 · Cited by 4 · see citing works

On the multiplicity of sugar transport systems in guinea pig jejunum.

Lostao, M. P., Berjón, A., Barber, A., & Ponz, F. (1992) · PubMed · Cited by 1 · see citing works

Molecular and metabolic mechanisms of insulin resistance and β-cell failure in type 2 diabetes

Muoio, D. M., & Newgard, C. B. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2327 · Cited by 1,177 · see citing works

Pathogenesis of insulin resistance in skeletal muscle

Abdul-Ghani, M. A., & DeFronzo, R. A. (2010) · Journal of Biomedicine and Biotechnology · doi:10.1155/2010/476279 · Cited by 670 · see citing works

Metabolites as regulators of insulin sensitivity and metabolism

Yang, Q., Vijayakumar, A., & Kahn, B. B. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0044-8 · Cited by 681 · see citing works

Failure of fat cell proliferation, mitochondrial function and fat oxidation results in ectopic fat storage, insulin resistance and type II diabetes mellitus

Heilbronn, L. K., Smith, S. R., & Ravussin, É. (2004) · International Journal of Obesity · doi:10.1038/sj.ijo.0802853 · Cited by 411 · see citing works

Troglitazone Inhibits Formation of Early Atherosclerotic Lesions in Diabetic and Nondiabetic Low Density Lipoprotein Receptor–Deficient Mice

Collins, A. R., Meehan, W. P., Kintscher, U., Jackson, S. M., Wakino, S., Noh, G. J., Palinski, W., Hsueh, W. A., & Law, R. E. (2001) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.21.3.365 · Cited by 384 · see citing works

Ectopic fat and insulin resistance: pathophysiology and effect of diet and lifestyle interventions.

Snel, M., Jonker, J. T., Schoones, J., Lamb, H., de Roos, A., Pijl, H., Smit, J. W. A., Meinders, A. E., & Jazet, I. M. (2012) · International Journal of Endocrinology · doi:10.1155/2012/983814 · Cited by 368 · see citing works

The metabolic syndrome: role of skeletal muscle metabolism.

Stump, C. S., Henriksen, E. J., Wei, Y., & Sowers, J. R. (2006) · Annals of Medicine · doi:10.1080/07853890600888413 · Cited by 362 · see citing works

Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control

Noland, R. C., Koves, T. R., Seiler, S. E., Lum, H., Lust, R. M., Ilkayeva, O., Stevens, R. D., Hegardt, F. G., & Muoio, D. M. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.032888 · Cited by 317 · see citing works

Role of a critical visceral adipose tissue threshold (CVATT) in metabolic syndrome: implications for controlling dietary carbohydrates: a review

Freedland, E. S. (2004) · Nutrition & Metabolism · doi:10.1186/1743-7075-1-12 · Cited by 296 · see citing works

Paradoxical resistance to diet-induced obesity in UCP1-deficient mice

Liu, X., Rossmeisl, M., McClaine, J. W., & Kozak, L. P. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200315737 · Cited by 281 · see citing works

Paradoxical resistance to diet-induced obesity in UCP1-deficient mice

Liu, X., Rossmeisl, M., McClaine, J. W., & Kozak, L. P. (2003) · Journal of Clinical Investigation · doi:10.1172/jci15737 · Cited by 265 · see citing works

Fat content in individual muscle fibers of lean and obese subjects.

Malenfant, P., Joanisse, D., Thériault, R., Goodpaster, B., Kelley, D., & Simoneau, J.-A. (2001) · International Journal of Obesity · doi:10.1038/sj.ijo.0801733 · Cited by 227 · see citing works

Dynamic changes in fat oxidation in human primary myocytes mirror metabolic characteristics of the donor

Ukropcova, B., McNeil, M., Sereda, O., de Jonge, L., Xie, H., Bray, G. A., & Smith, S. R. (2005) · Journal of Clinical Investigation · doi:10.1172/jci24332 · Cited by 213 · see citing works

Circadian Rhythms, the Molecular Clock, and Skeletal Muscle

Harfmann, B. D., Schroder, E. A., & Esser, K. A. (2015) · Journal of Biological Rhythms · doi:10.1177/0748730414561638 · Cited by 211 · see citing works

Exercise, Abdominal Obesity, Skeletal Muscle, and Metabolic Risk: Evidence for a Dose Response

Slentz, C. A., Houmard, J. A., & Kraus, W. E. (2009) · Obesity · doi:10.1038/oby.2009.385 · Cited by 202 · see citing works

Quercetin glucosides inhibit glucose uptake into brush-border-membrane vesicles of porcine jejunum

Cermak, R., Landgraf, S., & Wolffram, S. (2004) · British Journal Of Nutrition · doi:10.1079/bjn20041128 · Cited by 194 · see citing works

Tuning fatty acid oxidation in skeletal muscle with dietary fat and exercise

Fritzen, A. M., Lundsgaard, A.-M., & Kiens, B. (2020) · Nature Reviews Endocrinology · doi:10.1038/s41574-020-0405-1 · Cited by 180 · see citing works

The Role of Mammalian Sirtuins in the Regulation of Metabolism, Aging, and Longevity

Satoh, A., Stein, L. R., & Imai, S. (2011) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-21631-2_7 · Cited by 171 · see citing works

Lipid peroxidation in skeletal muscle of obese as compared to endurance-trained humans: a case of good vs. bad lipids?

Russell, A. P., Gastaldi, G., Bobbioni-Harsch, E., Arboit, P., Gobelet, C., Dériaz, O., Golay, A., Witztum, J. L., & Giacobino, J.-P. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)00875-5 · Cited by 166 · see citing works

Applications of stable, nonradioactive isotope tracers in in vivo human metabolic research

Kim, I.-Y., Suh, S., Lee, I., & Wolfe, R. R. (2016) · Experimental & Molecular Medicine · doi:10.1038/emm.2015.97 · Cited by 164 · see citing works

Skeletal muscle triglyceride: marker or mediator of obesity-induced insulin resistance in type 2 diabetes mellitus?

Goodpaster, B. H., & Kelley, D. E. (2002) · Current Diabetes Reports · doi:10.1007/s11892-002-0086-2 · Cited by 155 · see citing works

Untitled work

(2007) · doi:10.1139/h06-102 · Cited by 160 · see citing works

Increased mitochondrial fatty acid oxidation is sufficient to protect skeletal muscle cells from palmitate-induced apoptosis

Henique, C., Mansouri, A., Fumey, G., Lenoir, V., Girard, J., Bouillaud, F., Prip-Buus, C., & Cohen, I. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.170431 · Cited by 159 · see citing works

Adipose tissue macrophage populations and inflammation are associated with systemic inflammation and insulin resistance in obesity

Kunz, H., Hart, C. R., Gries, K. J., Parvizi, M., LAURENTI, M. C., Man, C. D., Moore, N., Zhang, X., Ryan, Z., Polley, E. C., et al. (2021) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00070.2021 · Cited by 163 · see citing works

Obesity-associated insulin resistance in skeletal muscle: Role of lipid accumulation and physical inactivity

Eckardt, K., Taube, A., & Eckel, J. (2011) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-011-9168-2 · Cited by 157 · see citing works

Insulin Resistance and Mitochondrial Dysfunction

González-Franquesa, A., & Patti, M. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-55330-6_25 · Cited by 154 · see citing works

Metabolic Syndrome as a Multifaceted Risk Factor for Oxidative Stress

Spahis, S., Borys, J.-M., & Levy, E. H. (2016) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6756 · Cited by 140 · see citing works

Adipokines as regulators of muscle metabolism and insulin sensitivityThis paper is one of a selection of papers published in this Special Issue, entitled 14th International Biochemistry of Exercise Conference – Muscles as Molecular and Metabolic Machines, and has undergone the Journal’s usual peer review process.

Dyck, D. J. (2009) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h09-037 · Cited by 136 · see citing works

Mirror, Mirror on the Wall: When the Postoperative Reflection Does Not Meet Patientsʼ Expectations

Rohrich, R. J. (2001) · Plastic and Reconstructive Surgery · doi:10.1097/00006534-200108000-00035 · Cited by 130 · see citing works

Mitochondrial dynamics as a bridge between mitochondrial dysfunction and insulin resistance

Zorzano, A., Liesa, M., & Palacı́n, M. (2009) · Archives of Physiology and Biochemistry · doi:10.1080/13813450802676335 · Cited by 123 · see citing works

Mitochondrial dysfunction in non-alcoholic fatty liver disease and insulin resistance: Cause or consequence?

García‐Ruiz, C., Baulies, A., Marı́, M., García-Rovés, P. M., & Fernández-Checa, J. C. (2013) · Free Radical Research · doi:10.3109/10715762.2013.830717 · Cited by 116 · see citing works

Mitochondrial Dysregulation in the Pathogenesis of Diabetes: Potential for Mitochondrial Biogenesis-Mediated Interventions

Joseph, A.-M., Joanisse, D. R., Baillot, R. G., & Hood, D. A. (2011) · Experimental Diabetes Research · doi:10.1155/2012/642038 · Cited by 117 · see citing works

iTRAQ-based proteomic analysis reveals key proteins affecting muscle growth and lipid deposition in pigs

Wang, Z., Shang, P., Li, Q., Wang, L., Chamba, Y., Zhang, B., Zhang, H., & Wu, C. (2017) · Scientific Reports · doi:10.1038/srep46717 · Cited by 111 · see citing works

The effect of an aerobic exercise bout 24 h prior to each doxorubicin treatment for breast cancer on markers of cardiotoxicity and treatment symptoms: a RCT

Kirkham, A. A., Eves, N. D., Shave, R., Bland, K. A., Bovard, J. M., Gelmon, K. A., Virani, S., McKenzie, D. C., Stöhr, E. J., Waburton, D. E. R., et al. (2017) · Breast Cancer Research and Treatment · doi:10.1007/s10549-017-4554-4 · Cited by 107 · see citing works

Adiposopathy: how do diet, exercise and weight loss drug therapies improve metabolic disease in overweight patients?

Bays, H. E., Blonde, L., & Rosenson, R. S. (2006) · Expert Review of Cardiovascular Therapy · doi:10.1586/14779072.4.6.871 · Cited by 102 · see citing works

Arctigenin, a natural compound, activates AMP-activated protein kinase via inhibition of mitochondria complex I and ameliorates metabolic disorders in ob/ob mice

Huang, S., Yu, R.-T., Gong, J., Feng, Y., Dai, Y.-L., Hu, F., Hu, Y., Tao, Y.-D., & Leng, Y. (2011) · Diabetologia · doi:10.1007/s00125-011-2366-3 · Cited by 104 · see citing works

Energy balance and pollution by organochlorines and polychlorinated biphenyls

Pelletier, C., Imbeault, P., & Tremblay, A. (2003) · Obesity Reviews · doi:10.1046/j.1467-789x.2003.00085.x · Cited by 100 · see citing works

Biomechanical, cardiorespiratory, metabolic and perceived responses to electrically assisted cycling

Sperlich, B., Zinner, C., Hébert‐Losier, K., Born, D., & Holmberg, H. (2012) · European Journal of Applied Physiology · doi:10.1007/s00421-012-2382-0 · Cited by 92 · see citing works

Posttranscriptional Control of Renin Synthesis

Skalweit, A., Doller, A., Huth, A., Kähne, T., Persson, P. B., & Thiele, B. (2003) · Circulation Research · doi:10.1161/01.res.0000059300.67152.4e · Cited by 89 · see citing works

Suppression of 5′-Nucleotidase Enzymes Promotes AMP-activated Protein Kinase (AMPK) Phosphorylation and Metabolism in Human and Mouse Skeletal Muscle

Kulkarni, S. S., Karlsson, H., Szekeres, F. L. M., Chibalin, A., Krook, A., & Zierath, J. R. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.268292 · Cited by 86 · see citing works

Direct Inhibitory Effect of Rotavirus NSP4(114-135) Peptide on the Na + - d -Glucose Symporter of Rabbit Intestinal Brush Border Membrane

Halaihel, N., Moal, V. L.-L., Ball, J. M., Estes, M. K., Alvarado, F., & Vasseur, M. (2000) · Journal of Virology · doi:10.1128/jvi.74.20.9464-9470.2000 · Cited by 86 · see citing works

Upregulation of peroxisome proliferator-activated receptor gamma coactivator gene (PGC1A) during weight loss is related to insulin sensitivity but not to energy expenditure

Gastaldi, G., Russell, A. P., Golay, A., Giacobino, J., Habicht, F., Barthassat, V., Muzzin, P., & Bobbioni-Harsch, E. (2007) · Diabetologia · doi:10.1007/s00125-007-0782-1 · Cited by 85 · see citing works

Skeletal Muscle Lipid and Its Association with Insulin Resistance: What Is the Role for Exercise?

Goodpaster, F. H., & Brown, F. F. (2005) · Exercise and Sport Sciences Reviews · doi:10.1097/00003677-200507000-00008 · Cited by 84 · see citing works

Fat oxidation at rest predicts peak fat oxidation during exercise and metabolic phenotype in overweight men

Rosenkilde, M., Nordby, P., Nielsen, L., Stallknecht, B., & Helge, J. (2010) · International Journal of Obesity · doi:10.1038/ijo.2010.11 · Cited by 79 · see citing works

What is “Hyper” in the ALS Hypermetabolism?

Ferri, A., & Coccurello, R. (2017) · Mediators of Inflammation · doi:10.1155/2017/7821672 · Cited by 77 · see citing works

Activation of PPAR-δ in isolated rat skeletal muscle switches fuel preference from glucose to fatty acids

Brunmair, B., Staniek, K., Dörig, J., Szöcs, Z., Stadlbauer, K., Marian, V., Gras, F., Anderwald, C. H., Nohl, H., Waldhäusl, W. K., et al. (2006) · Diabetologia · doi:10.1007/s00125-006-0357-6 · Cited by 78 · see citing works

Effects of obesity on lipid profiles in neutered male and female cats

Hoenig, M. E., Wilkins, C., Holson, J., & Ferguson, D. C. (2003) · American Journal of Veterinary Research · doi:10.2460/ajvr.2003.64.299 · Cited by 76 · see citing works

Fasting Respiratory Quotient as a Predictor of Long-Term Weight Changes in Non-Obese Women

Marra, M., Scalfi, L., Contaldo, F., & Pasanisi, F. (2004) · Annals of Nutrition and Metabolism · doi:10.1159/000079556 · Cited by 75 · see citing works

Adiposopathy: why do adiposity and obesity cause metabolic disease?

Bays, H. E., & Ballantyne, C. M. (2006) · Future Lipidology · doi:10.2217/17460875.1.4.389 · Cited by 73 · see citing works

Diabetes: mellitus or lipidus?

Shafrir, E., & Raz, I. (2003) · Diabetologia · doi:10.1007/s00125-003-1052-5 · Cited by 72 · see citing works

Mitochondrial fitness and insulin sensitivity in humans

Szendroedi, J., & Roden, M. (2008) · Diabetologia · doi:10.1007/s00125-008-1153-2 · Cited by 71 · see citing works

Skeletal Muscle Fat Oxidation Is Increased in African‐American and White Women after 10 days of Endurance Exercise Training

Cortright, R. N., Sandhoff, K. M., Basilio, J. L., Berggren, J. R., Hickner, R. C., Hulver, M. W., Dohm, G. L., & Houmard, J. A. (2006) · Obesity · doi:10.1038/oby.2006.137 · Cited by 70 · see citing works

Exercise as ‘precision medicine’ for insulin resistance and its progression to type 2 diabetes: a research review

DiMenna, F. J., & Arad, A. D. (2018) · BMC Sports Science, Medicine and Rehabilitation · doi:10.1186/s13102-018-0110-8 · Cited by 68 · see citing works

MAPK phosphatase-1 facilitates the loss of oxidative myofibers associated with obesity in mice

Flach, R. J. R., Le, A. M., Zhang, L., Kahn, M., Samuel, V. T., Shulman, G. I., & Bennett, A. M. (2009) · Journal of Clinical Investigation · doi:10.1172/jci39054 · Cited by 65 · see citing works

Lipotoxicity: the obese and endurance-trained paradox

Russell, A. P. (2004) · International Journal of Obesity · doi:10.1038/sj.ijo.0802859 · Cited by 64 · see citing works

Perilipin 2 and lipid droplets provide reciprocal stabilization

Xu, S., Zou, F., Diao, Z., Zhang, S., Deng, Y., Zhu, X., Cui, L., Yu, J., Zhang, Z., Bamigbade, A. T., et al. (2019) · Biophysics Reports · doi:10.1007/s41048-019-0091-5 · Cited by 63 · see citing works

L-Tryptophan Suppresses Rise in Blood Glucose and Preserves Insulin Secretion in Type-2 Diabetes Mellitus Rats

Inubushi, T., Kamemura, N., Oda, M., Sakùrai, J., Nakaya, Y., Harada, N., Suenaga, M., Matsunaga, Y., Ishidoh, K., & Katunuma, N. (2012) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.58.415 · Cited by 63 · see citing works

Intravenous acetate elicits a greater free fatty acid rebound in normal than hyperinsulinaemic humans

Fernandes, J., Vogt, J. A., & Wolever, T. M. S. (2012) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2012.98 · Cited by 58 · see citing works

Peroxisome proliferator-activated receptor-δ, a regulator of oxidative capacity, fuel switching and cholesterol transport

Fürnsinn, C., Willson, T. M., & Brunmair, B. (2006) · Diabetologia · doi:10.1007/s00125-006-0492-0 · Cited by 56 · see citing works

Expression of mRNA for glucose transport proteins in jejunum, liver, kidney and skeletal muscle of pigs

Aschenbach, J. R., Steglich, K., Gäbel, G., & Honscha, K. U. (2009) · Journal of Physiology and Biochemistry · doi:10.1007/bf03180578 · Cited by 54 · see citing works

Aerobic Exercise Is Necessary to Improve Glucose Utilization with Moderate Weight Loss in Women

Ryan, A. S., Nicklas, B. J., & Berman, D. M. (2006) · Obesity · doi:10.1038/oby.2006.122 · Cited by 53 · see citing works

Rotavirus infection impairs intestinal brush-border membrane Na+-solute cotransport activities in young rabbits

Halaihel, N., Moal, V. L.-L., Alvarado, F., & Vasseur, M. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.279.3.g587 · Cited by 54 · see citing works

The Impact of Rapid Weight Loss on Oxidative Stress Markers and the Expression of the Metabolic Syndrome in Obese Individuals

Tůmová, E., Sun, W., Jones, P. H., Vrablı́k, M., Ballantyne, C. M., & Hoogeveen, R. C. (2013) · Journal of Obesity · doi:10.1155/2013/729515 · Cited by 52 · see citing works

Skeletal muscle mitochondrial and metabolic responses to a high-fat diet in female rats bred for high and low aerobic capacity

Naples, S. P., Borengasser, S. J., Rector, R. S., Uptergrove, G. M., Morris, E. M., Mikus, C. R., Koch, L. G., Britton, S. L., Ibdah, J. A., & Thyfault, J. P. (2010) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h09-139 · Cited by 49 · see citing works

Nutraceutical Supplements for Weight Loss

Poddar, K. H., Kolge, S., Bezman, L., Mullin, G. E., & Cheskin, L. J. (2011) · Nutrition in Clinical Practice · doi:10.1177/0884533611419859 · Cited by 49 · see citing works

Increased mitochondrial respiration of adipocytes from metabolically unhealthy obese compared to healthy obese individuals

Böhm, A., Keuper, M., Meile, T., Zdichavsky, M., Fritsche, A., Häring, H., de Angelis, M. H., Staiger, H., & Frankó, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-69016-9 · Cited by 49 · see citing works

Prevention of Obesity in Young Children: A Critical Challenge for Medical Professionals

SOTHERN, M. S., & Gordon, S. T. (2003) · Clinical Pediatrics · doi:10.1177/000992280304200202 · Cited by 49 · see citing works

Comparison of Body Fat Composition and Serum Adiponectin Levels in Diabetic Obesity and Non‐diabetic Obesity

Kim, C. S., Park, J., Park, J. S., Kang, E. S., Ahn, C. W., Cha, B., Lim, S., Kim, K.-R., & Lee, H. (2006) · Obesity · doi:10.1038/oby.2006.133 · Cited by 46 · see citing works

Reduced whole-body lipid oxidation is associated with insulin resistance, but not with intramyocellular lipid content in offspring of type 2 diabetic patients

Lattuada, G., Costantino, F., Caumo, A., Scifo, P., Ragogna, F., COBELLI, F. D., Maschio, A. D., Luzi, L., & Perseghin, G. (2005) · Diabetologia · doi:10.1007/s00125-005-1686-6 · Cited by 44 · see citing works

Metabolism as a complex genetic trait, a systems biology approach: Implications for inborn errors of metabolism and clinical diseases

Vockley, J. E. (2008) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-008-1005-8 · Cited by 43 · see citing works

Reduced AMP-activated protein kinase activity in mouse skeletal muscle does not exacerbate the development of insulin resistance with obesity

Beck Jørgensen, S., O’Neill, H. M., Hewitt, K., Kemp, B. E., & Steinberg, G. R. (2009) · Diabetologia · doi:10.1007/s00125-009-1483-8 · Cited by 42 · see citing works

High-intensity exercise and carbohydrate-reduced energy-restricted diet in obese individuals

Sartor, F., de Morree, H. M., MATSCHKE, V., Marcora, S., Milousis, A., Thom, J. M., & Kubis, H. (2010) · European Journal of Applied Physiology · doi:10.1007/s00421-010-1571-y · Cited by 42 · see citing works

The Mitochondrial tRNALeu(UUR) A3302G Mutation may be Associated With Insulin Resistance in Woman With Polycystic Ovary Syndrome

Ding, Y., Zhuo, G., & Zhang, C. (2015) · Reproductive Sciences · doi:10.1177/1933719115602777 · Cited by 39 · see citing works

High-Fat- and Lipid-Induced Insulin Resistance in Rats: The Comparison of Glucose Metabolism, Plasma Resistin and Adiponectin Levels

Li, L., Yang, G., Li, Q., Tang, Y., & Li, K. (2006) · Annals of Nutrition and Metabolism · doi:10.1159/000098141 · Cited by 36 · see citing works

Adipogenic potential of skeletal muscle satellite cells

Sanna, M., Franzin, C., Pozzobon, M., Favaretto, F., Rossi, C. A., Calcagno, A., Scarda, A., Prà, C. D., Pilon, C., Milan, G., et al. (2009) · Clinical Lipidology · doi:10.2217/clp.09.8 · Cited by 36 · see citing works

A decreased<i>n</i>-6/<i>n</i>-3 ratio in the fat-1 mouse is associated with improved glucose tolerance

Smith, B. K., Holloway, G. P., Reza-Lopez, S., Jeram, S. M., Kang, J. X., & Ma, D. W. L. (2010) · Applied Physiology Nutrition and Metabolism · doi:10.1139/h10-066 · Cited by 35 · see citing works

Inhibition of acetyl-CoA carboxylase 2 enhances skeletal muscle fatty acid oxidation and improves whole-body glucose homeostasis in db/db mice

Glund, S., Schoelch, C., Thomas, L. H., Niessen, H. G., Stiller, D., Roth, G. J., & Neubauer, H. (2012) · Diabetologia · doi:10.1007/s00125-012-2554-9 · Cited by 35 · see citing works

Effect of a low-starch/low-dairy diet on fat oxidation in overweight and obese women with polycystic ovary syndrome

Pohlmeier, A. M., Phy, J. L., Watkins, P., Boylan, M., Spallholz, J., Harris, K. S., & Cooper, J. A. (2014) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2014-0073 · Cited by 34 · see citing works

Altered mitochondrial network morphology and regulatory proteins in mitochondrial quality control in myotubes from severely obese humans with or without type 2 diabetes

Gundersen, A. E., Kugler, B. A., McDonald, P. M., Veraksa, A. N., Houmard, J. A., & Zou, K. (2019) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2019-0208 · Cited by 34 · see citing works

Insulin Resistance: Pathophysiology and Rationale for Treatment

Muntoni, S., & Muntoni, S. (2011) · Annals of Nutrition and Metabolism · doi:10.1159/000323395 · Cited by 33 · see citing works

Emerging paradigms for understanding fatness and diabetes risk

Smith, S. R., & Ravussin, É. (2002) · Current Diabetes Reports · doi:10.1007/s11892-002-0087-1 · Cited by 34 · see citing works

Controlling the release and production of renin

Persson, P. B., Skalweit, A., & Thiele, B. J. (2004) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.2004.01308.x · Cited by 33 · see citing works

Carbohydrate intake and glycemic index affect substrate oxidation during a controlled weight cycle in healthy men

Kahlhöfer, J., Lagerpusch, M., Enderle, J., Eggeling, B., Braun, W., Pape, D., Müller, M. J., & Bosy‐Westphal, A. (2014) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2014.132 · Cited by 31 · see citing works

Metabolic Inflexibility in Skeletal Muscle: A Prelude to the Cardiometabolic Syndrome?

Thyfault, J. P., Rector, R. S., & Noland, R. C. (2006) · Journal of the CardioMetabolic Syndrome · doi:10.1111/j.1559-4564.2006.05629.x · Cited by 31 · see citing works

Fat oxidation over a range of exercise intensities: fitness versus fatness

Croci, I., Hickman, I. J., Wood, R. E., Borrani, F., Macdonald, G. A., & Byrne, N. M. (2014) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2014-0144 · Cited by 30 · see citing works

Current Views of the Fat Cell as an Endocrine Cell: Lipotoxicity

Tchkonia, T., Corkey, B. E., & Kirkland, J. L. (2007) · Springer eBooks · doi:10.1007/978-0-387-32164-6_6 · Cited by 30 · see citing works

Glucose oversupply increases Δ9-desaturase expression and its metabolites in rat skeletal muscle

Houdali, B., Wahl, H. G., Kresi, M., Nguyen, V., Haap, M. M., Machicao, F. E., Ammon, H. P. T., Renn, W., Schleicher, E. D., & Häring, H. (2003) · Diabetologia · doi:10.1007/s00125-002-1015-2 · Cited by 30 · see citing works

Metabolic inflexibility in women with polycystic ovary syndrome: a systematic review

Rimmer, M., Tan, B. K., Teede, H., Thangaratinam, S., & H. Al Wattar, B. (2020) · Gynecological Endocrinology · doi:10.1080/09513590.2019.1698025 · Cited by 29 · see citing works

Influence of maximal fat oxidation on long-term weight loss maintenance in humans

Dandanell, S., Husted, K., Amdisen, S., Vigelsø, A., Dela, F., Larsen, S., & Helge, J. W. (2017) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00270.2017 · Cited by 29 · see citing works

Subcellular localisation and composition of intramuscular triacylglycerol influence insulin sensitivity in humans

KAHN, D. E., Perreault, L., Macias, E., Zarini, S., Newsom, S. A., Strauss, A., Kerege, A. A., Harrison, K. A., Snell‐Bergeon, J. K., & Bergman, B. C. (2020) · Diabetologia · doi:10.1007/s00125-020-05315-0 · Cited by 28 · see citing works

cAMP controls human renin mRNA stability via specific RNA‐binding proteins

Morris, B. J., Adams, D. J., Beveridge, D. J., van der Weyden, L., Mangs, H., & Leedman, P. J. (2004) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.2004.01307.x · Cited by 28 · see citing works

Transport of nutrients and electrolytes across the intestinal wall in pigs

Breves, G., Kock, J., & Schröder, B. (2007) · Livestock Science · doi:10.1016/j.livsci.2007.01.021 · Cited by 27 · see citing works

Low back pain risk factors in a large rural Australian Aboriginal community. An opportunity for managing co-morbidities?

Vindigni, D., Walker, B. F., Jamison, J. R., Costa, C. D., Parkinson, L., & Blunden, S. V. (2005) · Chiropractic & Manual Therapies · doi:10.1186/1746-1340-13-21 · Cited by 27 · see citing works

Effects of weight loss and calorie restriction on carbohydrate metabolism

Manco, M., & Mingrone, G. (2005) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/01.mco.0000172585.09762.8e · Cited by 27 · see citing works

Expression of genes regulating Malonyl‐CoA in human skeletal muscle

Pender, C., Trentadue, A. R., Pories, W. J., Dohm, G. L., Houmard, J. A., & YOUNGREN, J. F. (2006) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20944 · Cited by 27 · see citing works

REPTOR and CREBRF encode key regulators of muscle energy metabolism

Saavedra, P., Dumesic, P. A., Hu, Y., Filine, E., Jouandin, P., Binari, R. C., Wilensky, S. E., Rodiger, J., Wang, H., Chen, W., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40595-1 · Cited by 26 · see citing works

GLP-1 agonist-based therapies: An emerging new class of antidiabetic drug with potential cardioprotective effects

Sulistio, M. S., Carothers, C., Mangat, M., Lujan, M., OLIVEROS, R. A., & CHILTON, R. J. (2009) · Current Atherosclerosis Reports · doi:10.1007/s11883-009-0015-9 · Cited by 26 · see citing works

FAK tyrosine phosphorylation is regulated by AMPK and controls metabolism in human skeletal muscle

Lassiter, D. G., Nylén, C., Sjögren, R. J. O., Chibalin, A., Wallberg‐Henriksson, H., Näslund, E. B., Krook, A., & Zierath, J. R. (2017) · Diabetologia · doi:10.1007/s00125-017-4451-8 · Cited by 26 · see citing works

Cellular and Biochemical Features of Skeletal Muscle in Obese Yucatan Minipigs

Guillerm-Regost, C., Louveau, I., Sebert, S. P., Damon, M., Champ, M. M. J., & Gondret, F. (2006) · Obesity · doi:10.1038/oby.2006.195 · Cited by 26 · see citing works

Mitochondrial function and dysfunction in exercise and insulin resistanceThis paper article is one of a selection of papers published in this Special Issue, entitled 14th International Biochemistry of Exercise Conference – Muscles as Molecular and Metabolic Machines, and has undergone the Journal’s usual peer review process.

Holloway, G. P. (2009) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h09-028 · Cited by 25 · see citing works

Independent modulation by food supply of two distinct sodium-activated D-glucose transport systems in the guinea pig jejunal brush-border membrane.

Brot‐Laroche, E., Dao, M. T., Alcalde, A. I., Delhomme, B., Triadou, N., & Alvarado, F. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.17.6370 · Cited by 36 · see citing works

Separation of two distinct Na+/d-glucose cotransport systems in the human fetal jejunum by means of their differential specificity for 3-O-methylglucose

Malo, C. (1990) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(90)90394-4 · Cited by 38 · see citing works

Temperature sensitivity and substrate specificity of two distinct Na+-activated D-glucose transport systems in guinea pig jejunal brush border membrane vesicles.

Brot‐Laroche, E., Serrano, M. A., Delhomme, B., & Alvarado, F. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)84544-1 · Cited by 73 · see citing works

Ontogeny of Na+/D-glucose cotransport in guinea-pig jejunal vesicles: only one system is involved at both 20°C and 35°C

Malo, C. (1993) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(93)90419-z · Cited by 8 · see citing works

On the multiplicity of sugar transport systems in guinea pig jejunum.

Lostao, M. P., Berjón, A., Barber, A., & Ponz, F. (1992) · PubMed · Cited by 1 · see citing works