Mitochondrial tissue specificity of substrates utilization in rat cardiac and skeletal muscles

Biochemical Adaptations to Endurance Exercise in Muscle

Holloszy, J. O., & Booth, F. W. (1976) · Annual Review of Physiology · doi:10.1146/annurev.ph.38.030176.001421 · Cited by 1,053 · see citing works

Molecular basis of skeletal muscle plasticity-from gene to form and function

Flück, M., & Hoppeler, H. H. (2003) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/s10254-002-0004-7 · Cited by 476 · see citing works

Role of mitochondrial lactate dehydrogenase and lactate oxidation in the intracellular lactate shuttle

Brooks, G. A., Dubouchaud, H., Brown, M. A., Sicurello, J. P., & Butz, C. E. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.3.1129 · Cited by 470 · see citing works

Respiratory capacity of white, red, and intermediate muscle: adaptative response to exercise

Baldwin, K., Klinkerfuss, G., Terjung, R. L., Mole, P. A., & Holloszy, J. O. (1972) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1972.222.2.373 · Cited by 450 · see citing works

Endurance training, expression, and physiology of LDH, MCT1, and MCT4 in human skeletal muscle

Dubouchaud, H., Butterfield, G. E., Wolfel, E. E., Bergman, B. C., & Brooks, G. A. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.278.4.e571 · Cited by 384 · see citing works

Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo

Saks, V. A., Veksler, V., Kuznetsov, A. V., Kay, L., Sikk, P., Tiivel, T., Tranqui, L., Olivares, J., Winkler, K., Wiedemann, F. R., et al. (1998) · Springer eBooks · doi:10.1007/978-1-4615-5653-4_7 · Cited by 361 · see citing works

Mitochondrial respiratory parameters in cardiac tissue: A novel method of assessment by using saponin-skinned fibers

Veksler, V., Kuznetsov, A. V., Sharov, V. G., Kapelko, V. I., & Saks, V. A. (1987) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(87)90174-5 · Cited by 360 · see citing works

Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vitro

Veksler, V., Kuznetsov, A. V., Kay, L., Sikk, P., Tiivel, T., Tranqui, L., Olivares, J., Winkler, K., Wiedemann, F. R., & Kunz, W. S. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006834912257 · Cited by 308 · see citing works

Role of creatine phosphokinase in cellular function and metabolism

Saks, V. A., Rosenshtraukh, L. V., Smirnov, V. N., & Чазов, Е. И. (1978) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y78-113 · Cited by 303 · see citing works

Oxidative capacity of muscle and mitochondria: correlation of physiological, biochemical, and morphometric characteristics.

Schwerzmann, K., Hoppeler, H. H., Kayar, S. R., & Weibel, E. R. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.5.1583 · Cited by 272 · see citing works

Energy Metabolism in the Normal and Failing Heart: Potential for Therapeutic Interventions

Stanley, W. C., & Chandler, M. P. (2002) · Heart Failure Reviews · doi:10.1023/a:1015320423577 · Cited by 271 · see citing works

Mammalian fuel utilization during sustained exercise

Brooks, G. A. (1998) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s0305-0491(98)00025-x · Cited by 253 · see citing works

Energetic Crosstalk Between Organelles

Kaasik, A., Veksler, V., Boehm, E. A., Novotová, M., Minajeva, A., & Ventura‐Clapier, R. (2001) · Circulation Research · doi:10.1161/hh1401.093440 · Cited by 252 · see citing works

Palmitate transport and fatty acid transporters in red and white muscles

Bonen, A., Luiken, J. J. F. P., Liu, S., Dyck, D. J., Kiens, B., Kristiansen, S., Turcotte, L. P., Vusse, G. J., & Glatz, J. F. C. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.275.3.e471 · Cited by 228 · see citing works

Tissue variation in the control of oxidative phosphorylation: Implication for mitochondrial diseases

ROSSIGNOL, R., LETELLIER, T., MALGAT, M., ROCHER, C., & MAZAT, J.-P. (2000) · Biochemical Journal · doi:10.1042/bj3470045 · Cited by 202 · see citing works

Striking Differences Between the Kinetics of Regulation of Respiration by ADP in Slow‐Twitch and Fast‐Twitch Muscles In Vivo

Kuznetsov, A. V., Tiivel, T., Sikk, P., Käämbre, T., Kay, L., Daneshrad, Z., Rossi, A., Kadaja, L., Peet, N., Seppet, E. K., et al. (1996) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1996.00909.x · Cited by 195 · see citing works

Intracellular energetic units in red muscle cells

Saks, V. A., Käämbre, T., Sikk, P., Eimre, M., Orlova, E., Paju, K., Piirsoo, A., Appaix, F., Kay, L., Regitz‐Zagrosek, V., et al. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3560643 · Cited by 187 · see citing works

Functional differences in lipid metabolism in resting skeletal muscle of various fiber types

Dyck, D. J., Peters, S. J., Glatz, J. F. C., Górski, J., KEIZER, H. A., Kiens, B., Liu, S., Richter, E. A., Spriet, L. L., Vusse, G. J., et al. (1997) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1997.272.3.e340 · Cited by 186 · see citing works

Cardiac and skeletal muscle mitochondria have a monocarboxylate transporter MCT1

Brooks, G. A., Brown, M. A., Butz, C. E., Sicurello, J. P., & Dubouchaud, H. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.5.1713 · Cited by 185 · see citing works

Muscle Creatine Kinase-deficient Mice

Veksler, V., Kuznetsov, A. V., Anflous, K., Matéo, P., van Deursen, J., Wieringa, B., & Ventura‐Clapier, R. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.34.19921 · Cited by 185 · see citing works

Voltage—clamp analysis of the early current in frog skeletal muscle fibre using the double sucrose‐gap method

Ildefonse, M., & Rougier, O. (1972) · The Journal of Physiology · doi:10.1113/jphysiol.1972.sp009803 · Cited by 182 · see citing works

Characteristics of mitochondria isolated from type I and type IIb skeletal muscle

Jackman, M. R., & Willis, W. T. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.270.2.c673 · Cited by 173 · see citing works

Muscle Creatine Kinase-deficient Mice

Ventura‐Clapier, R., Kuznetsov, A. V., d’Albis, A., van Deursen, J., Wieringa, B., & Veksler, V. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.34.19914 · Cited by 141 · see citing works

Functional coupling of creatine kinases in muscles: Species and tissue specificity

Ventura‐Clapier, R., Kuznetsov, A. V., Veksler, V., Boehm, E. A., & Anflous, K. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006840508139 · Cited by 140 · see citing works

Intracellular energetic units in red muscle cells

Saks, V. A., Käämbre, T., Sikk, P., et al. (2001) · Biochemical Journal · doi:10.1042/bj3560643 · Cited by 134 · see citing works

Relationship between mitochondria and oxygen consumption in isolated cat muscles.

Hoppeler, H. H., HUDLICKÁ, O., & Uhlmann, E. (1987) · The Journal of Physiology · doi:10.1113/jphysiol.1987.sp016513 · Cited by 123 · see citing works

Fiber-type differences in muscle mitochondrial profiles

Leary, S. C., Lyons, C. N., Rosenberger, A. G., Ballantyne, J. S., Stillman, J. H., & Moyes, C. D. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00058.2003 · Cited by 96 · see citing works

Lactate dehydrogenase in rat mitochondria

Brandt, R. B., Laux, J. E., Spainhour, S. E., & Kline, E. S. (1987) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(87)90507-8 · Cited by 95 · see citing works

Mitochondrial oxidative function in human saponin‐skinned muscle fibres: effects of prolonged exercise

Tonkonogi, M., Harris, B. A., & Sahlin, K. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.279bz.x · Cited by 92 · see citing works

Metabolism—the lost child of cardiology∗∗Editorials published in the Journal of the American College of Cardiology reflect the views of the authors and do not necessarily represent the views of JACC or the American College of Cardiology.

Taegtmeyer, H. (2000) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(00)00870-6 · Cited by 85 · see citing works

No evidence of an intracellular lactate shuttle in rat skeletal muscle

Sahlin, K., Fernström, M., Svensson, M., & Tonkonogi, M. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.016683 · Cited by 81 · see citing works

Quantitative and qualitative adaptation of skeletal muscle mitochondria to increased physical activity

Zoll, J., Koulmann, N., Bahi, L., Ventura‐Clapier, R., & Bigard, A. X. (2002) · Journal of Cellular Physiology · doi:10.1002/jcp.10224 · Cited by 80 · see citing works

Lactate dehydrogenase is not a mitochondrial enzyme in human and mouse vastus lateralis muscle

Rasmussen, H., van Hall, G., & Rasmussen, U. F. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.019216 · Cited by 70 · see citing works

Lactate shuttle – between but not within cells?

Brooks, G. A. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.023705 · Cited by 62 · see citing works

l-Lactate transport into rat heart mitochondria and reconstruction of the l-lactate/pyruvate shuttle

Valenti, D., Lidia de, B. A. R. I., Atlante, A., & Passarella, S. (2002) · Biochemical Journal · doi:10.1042/bj3640101 · Cited by 48 · see citing works

Enzyme levels of the NADH shuttle systems: measurements in isolated muscle fibres from humans of differing physical activity

Schantz, P., & Henriksson, J. (1987) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1987.tb08090.x · Cited by 48 · see citing works

Carbohydrate and fat in energy metabolism of red and white muscle

Pande, S., & Mc, B. (1971) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1971.220.2.549 · Cited by 44 · see citing works

Evaluation of quantitative and qualitative aspects of mitochondrial function in human skeletal and cardiac muscles

N’guessan, B. B., Zoll, J., Ribera, F., Ponsot, E., Lampert, E., Ventura‐Clapier, R., Veksler, V., & Mettauer, B. (2003) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000009874.14649.ca · Cited by 33 · see citing works

Capacity of oxidative phosphorylation in human skeletal muscle

Gnaiger, E. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.03.013 · Cited by 446 · see citing works

Lactate metabolism: historical context, prior misinterpretations, and current understanding

Ferguson, B. S., Rogatzki, M. J., Goodwin, M. L., Kane, D. A., Rightmire, Z. B., & Gladden, L. B. (2018) · European Journal of Applied Physiology · doi:10.1007/s00421-017-3795-6 · Cited by 451 · see citing works

Lactate kinetics in human tissues at rest and during exercise

van Hall, G. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02122.x · Cited by 346 · see citing works

Colocalization of MCT1, CD147, and LDH in mitochondrial inner membrane of L6 muscle cells: evidence of a mitochondrial lactate oxidation complex

Hashimoto, T., Hussien, R., & Brooks, G. A. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00594.2005 · Cited by 253 · see citing works

Mitochondrial functional specialization in glycolytic and oxidative muscle fibers: tailoring the organelle for optimal function

Picard, M., Hepple, R. T., & Burelle, Y. (2012) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00368.2011 · Cited by 214 · see citing works

Mitochondrial lactate metabolism: history and implications for exercise and disease

Glancy, B. C., Kane, D. A., Kavazis, A. N., Goodwin, M. L., Willis, W. T., & Gladden, L. B. (2020) · The Journal of Physiology · doi:10.1113/jp278930 · Cited by 203 · see citing works

Palmitate increases superoxide production through mitochondrial electron transport chain and NADPH oxidase activity in skeletal muscle cells

Lambertucci, R. H., Hirabara, S. M., Silveira, L. R., Levada‐Pires, A. C., Curi, R., & Pithon‐Curi, T. C. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21463 · Cited by 187 · see citing works

Mitochondrial Lactate Oxidation Complex and an Adaptive Role for Lactate Production

Hashimoto, T., & Brooks, G. A. (2008) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e31815fcb04 · Cited by 174 · see citing works

Mitochondria and l ‐lactate metabolism

Passarella, S., Lidia de, B. A. R. I., Valenti, D., Pizzuto, R., Paventi, G., & Atlante, A. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.09.042 · Cited by 169 · see citing works

Simvastatin Effects on Skeletal Muscle

Larsen, S., Stride, N., Hey-Mogensen, M., Hansen, C. N., Bang, L. E., Bundgaard, H., Nielsen, L. B., Helge, J. W., & Dela, F. (2013) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2012.09.036 · Cited by 165 · see citing works

Chronology of mitochondrial and cellular events during skeletal muscle ischemia-reperfusion

Paradis, S., Charles, A., Meyer, A., Lejay, A., Scholey, J. W., Chakfé, N., Zoll, J., & Gény, B. (2016) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00356.2015 · Cited by 145 · see citing works

Estrogens, Estrogen Receptors Effects on Cardiac and Skeletal Muscle Mitochondria

Ventura‐Clapier, R., Piquereau, J., Veksler, V., & Garnier, A. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00557 · Cited by 134 · see citing works

Tracing the lactate shuttle to the mitochondrial reticulum

Brooks, G. A., Curl, C. C., Leija, R. G., Osmond, A. D., Duong, J. J., & Arevalo, J. A. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00802-3 · Cited by 110 · see citing works

Training at high exercise intensity promotes qualitative adaptations of mitochondrial function in human skeletal muscle

Daussin, F., Zoll, J., Ponsot, E., Dufour, S. P., Doutreleau, S., Lonsdorfer‐Wolf, E., Ventura‐Clapier, R., Mettauer, B., Piquard, F., Gény, B., et al. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01135.2007 · Cited by 106 · see citing works

Metabolic Implications of Dietary Trans‐fatty Acids

Dorfman, S. E., Didier, L., Gounarides, J., Li, X., Mullarkey, T. L., Rocheford, E. C., Sari‐Sarraf, F., Hirsch, E. A., Hughes, T. E., & Commerford, S. R. (2009) · Obesity · doi:10.1038/oby.2008.662 · Cited by 100 · see citing works

PGC-1α increases skeletal muscle lactate uptake by increasing the expression of MCT1 but not MCT2 or MCT4

Benton, C. R., Yoshida, Y., Lally, J., Han, X.-X., Hatta, H., & Bonen, A. (2008) · Physiological Genomics · doi:10.1152/physiolgenomics.90217.2008 · Cited by 97 · see citing works

Metabolic reprogramming by the pyruvate dehydrogenase kinase–lactic acid axis: Linking metabolism and diverse neuropathophysiologies

Jha, M. K., Lee, I., & Suk, K. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.006 · Cited by 89 · see citing works

Negligible direct lactate oxidation in subsarcolemmal and intermyofibrillar mitochondria obtained from red and white rat skeletal muscle

Yoshida, Y., Holloway, G. P., Ljubicic, V., Hatta, H., Spriet, L. L., Hood, D. A., & Bonen, A. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.135095 · Cited by 82 · see citing works

Time‐dependent effects of fatty acids on skeletal muscle metabolism

Hirabara, S. M., Silveira, L. R., Abdulkader, F., Carvalho, C. R. D. O., Procópio, J., & Curi, R. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20811 · Cited by 80 · see citing works

Cerebral glycolysis: a century of persistent misunderstanding and misconception

Schurr, A. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00360 · Cited by 80 · see citing works

Role of estrogen on skeletal muscle mitochondrial function in ovariectomized rats: a time course study in different fiber types

Cavalcanti‐de‐Albuquerque, J. P., Salvador, I. C., Martins, E. L., Messeder, D. J., Werneck‐de‐Castro, J. P., Galina, A., & de Carvalho, D. P. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00121.2013 · Cited by 79 · see citing works

ACE inhibition prevents myocardial infarction-induced skeletal muscle mitochondrial dysfunction

Zoll, J., Monassier, L., Garnier, A., N’guessan, B. B., Mettauer, B., Veksler, V., Piquard, F., Ventura‐Clapier, R., & Gény, B. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01486.2005 · Cited by 75 · see citing works

Lactate oxidation in human skeletal muscle mitochondria

Jacobs, R. A., Meinild, A., Nordsborg, N. B., & Lundby, C. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00476.2012 · Cited by 77 · see citing works

Increased mitochondrial substrate sensitivity in skeletal muscle of patients with type 2 diabetes.

Larsen, S., Stride, N., Hey-Mogensen, M., Hansen, C. N., Andersen, J. L., Madsbad, S., Worm, D., Helge, J. W., & Dela, F. (2011) · Diabetologia · doi:10.1007/s00125-011-2098-4 · Cited by 73 · see citing works

Heart failure: a model of cardiac and skeletal muscle energetic failure

Mettauer, B., Zoll, J., Garnier, A., & Ventura‐Clapier, R. (2006) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-006-0072-7 · Cited by 72 · see citing works

Structural and functional characterization of simvastatin-induced myotoxicity in different skeletal muscles

Özek, N. Ş., Bal, I. B., Sara, Y., Onur, R., & Severcan, F. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.09.010 · Cited by 69 · see citing works

The mitochondrial L-lactate dehydrogenase affair

Passarella, S., Paventi, G., & Pizzuto, R. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00407 · Cited by 69 · see citing works

The C57Bl/6 mouse serves as a suitable model of human skeletal muscle mitochondrial function

Jacobs, R. A., Díaz, V., Meinild, A., Gassmann, M., & Lundby, C. (2012) · Experimental Physiology · doi:10.1113/expphysiol.2012.070037 · Cited by 68 · see citing works

Training-induced improvement in lipid oxidation in type 2 diabetes mellitus is related to alterations in muscle mitochondrial activity. Effect of endurance training in type 2 diabetes

Bordenave, S., Metz, L., Flavier, S., Lambert, K., Ghanassia, É., Dupuy, A., Michel, F., Puech-Cathala, A.-M., de Mauverger, É. R., Brun, J. ‐., et al. (2008) · Diabetes & Metabolism · doi:10.1016/j.diabet.2007.11.006 · Cited by 66 · see citing works

The influence of age and aerobic fitness: effects on mitochondrial respiration in skeletal muscle

Larsen, S., Hey‐Mogensen, M., Rabøl, R., Stride, N., Helge, J. W., & Dela, F. (2012) · Acta Physiologica · doi:10.1111/j.1748-1716.2012.02408.x · Cited by 63 · see citing works

Freshly isolated mitochondria from failing human hearts exhibit preserved respiratory function

Cordero‐Reyes, A. M., Gupte, A. A., Youker, K. A., Loebe, M. M., Hsueh, W. A., Torre‐Amione, G., Taegtmeyer, H., & Hamilton, D. J. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2013.12.029 · Cited by 59 · see citing works

200th Anniversary of Lactate Research in Muscle

Gladden, L. B. (2008) · Exercise and Sport Sciences Reviews · doi:10.1097/jes.0b013e31817c0038 · Cited by 56 · see citing works

AMP-Activated Protein Kinase α2 Deficiency Affects Cardiac Cardiolipin Homeostasis and Mitochondrial Function

Athéa, Y., Viollet, B., Matéo, P., Rousseau‐Ralliard, D., Novotová, M., Garnier, A., Vaulont, S., Wilding, J. R., Grynberg, A., Veksler, V., et al. (2007) · Diabetes · doi:10.2337/db06-0187 · Cited by 55 · see citing works

Stimulus specific changes of energy metabolism in hypertrophied heart

Rimbaud, S., Sanchez, H., Garnier, A., Fortin, D., Bigard, X. A., Veksler, V., & Ventura‐Clapier, R. (2009) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2009.01.013 · Cited by 54 · see citing works

Glucose stimulates protein synthesis in skeletal muscle of neonatal pigs through an AMPK- and mTOR-independent process

Jeyapalan, A. S., Orellana, R. A., Suryawan, A., O’Connor, P. M. J., Nguyen, H. V., Escobar, J., Frank, J. W., & Davis, T. A. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00121.2007 · Cited by 51 · see citing works

Physical and Functional Association of Lactate Dehydrogenase (LDH) with Skeletal Muscle Mitochondria

Elustondo, P. A., White, A. E., Hughes, M. E., Brebner, K., Pavlov, E. V., & Kane, D. A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.476648 · Cited by 49 · see citing works

Intracellular Shuttle: The Lactate Aerobic Metabolism

Cruz, R. S. D. O., de Aguiar, R. A., Turnes, T., dos Santos, R. P., de Oliveira, M. F. M., & Caputo, F. (2012) · The Scientific World JOURNAL · doi:10.1100/2012/420984 · Cited by 48 · see citing works

Lactate: valuable for physical performance and maintenance of brain function during exercise

Todd, J. J. (2014) · Bioscience Horizons The International Journal of Student Research · doi:10.1093/biohorizons/hzu001 · Cited by 44 · see citing works

Exercise-induced mitochondrial dysfunction: a myth or reality?

Ostojić, S. M. (2016) · Clinical Science · doi:10.1042/cs20160200 · Cited by 37 · see citing works

Effects of Maternal Exercise Modes on Glucose and Lipid Metabolism in Offspring Stem Cells

Jevtovic, F., Zheng, D., Houmard, J. A., Krassovskaia, P. M., Lopez, C. A., Wisseman, B., Steen, D. M., Broskey, N. T., Isler, C. M., DeVente, J., et al. (2023) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgad059 · Cited by 33 · see citing works

Maternal exercise modifies body composition and energy substrates handling in male offspring fed a high-fat/high-sucrose diet

Quiclet, C., Dubouchaud, H., Berthon, P., Sanchez, H., Vial, G., Siti, F., Fontaine, E., Batandier, C., & Couturier, K. (2017) · The Journal of Physiology · doi:10.1113/jp274739 · Cited by 31 · see citing works

Cardio-protective effects of carnitine in streptozotocin-induced diabetic rats

Malone, J. I., Cuthbertson, D. D., Malone, M. A., & Schocken, D. D. (2006) · Cardiovascular Diabetology · doi:10.1186/1475-2840-5-2 · Cited by 26 · see citing works

Extra-nuclear telomerase reverse transcriptase (TERT) regulates glucose transport in skeletal muscle cells

Shaheen, F., Grammatopoulos, D. K., Müller, J., Zammit, V. A., & Lehnert, H. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.06.018 · Cited by 26 · see citing works

Lactate, Not Pyruvate, Is the End Product of Glucose Metabolism via Glycolysis

Schurr, A. (2017) · InTech eBooks · doi:10.5772/66699 · Cited by 24 · see citing works

Impact of experimental obesity on diaphragm structure, function, and bioenergetics

Rodrigues, G. C., Rocha, N. N., Maia, L. D. A., Melo, I. D. S., Simões, A. C., Antunes, M. A., Bloise, F. F., Woyames, J., da‐Silva, W. S., Capelozzi, V. L., et al. (2020) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00262.2020 · Cited by 20 · see citing works

The blood lactate/pyruvate equilibrium affair

Brooks, G. A., Osmond, A. D., Leija, R. G., Curl, C. C., Arevalo, J. A., Duong, J. J., & Horning, M. A. (2021) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00270.2021 · Cited by 20 · see citing works

Expression of UCP2 in Wistar rats varies according to age and the severity of obesity

Pheiffer, C., Jacobs, C., Patel, O., Ghoor, S., Muller, C. J. F., & Louw, J. (2015) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-015-0454-4 · Cited by 20 · see citing works

Characterization of Mitochondrial Content and Respiratory Capacities of Broiler Chicken Skeletal Muscles with Different Muscle Fiber Compositions

Hakamata, Y., Watanabe, K., Amo, T., Toyomizu, M., & Kikusato, M. (2018) · The Journal of Poultry Science · doi:10.2141/jpsa.0170141 · Cited by 20 · see citing works

Mitochondrial and energetic cardiac phenotype in hypothyroid rat. Relevance to heart failure

Athéa, Y., Garnier, A., Fortin, D., Bahi, L., Veksler, V., & Ventura‐Clapier, R. (2007) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-007-0307-2 · Cited by 18 · see citing works

Effects of cigarette smoke on in situ mitochondrial substrate oxidation of slow- and fast-twitch skeletal muscles

Decker, S. T., Matias, A. A., Bannon, S. T., Madden, J. P., Alexandrou-Majaj, N., & Layec, G. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121376 · Cited by 17 · see citing works

Sexual Preferences in Nutrient Utilization Regulate Oxygen Consumption and Reactive Oxygen Species Generation in Schistosoma mansoni: Potential Implications for Parasite Redox Biology

Oliveira, M., Soares, J. B. R. C., & de Oliveira, M. F. (2016) · PLoS ONE · doi:10.1371/journal.pone.0158429 · Cited by 17 · see citing works

Phosphocreatine resynthesis during recovery in different muscles of the exercising leg by 31 P ‐ MRS

Yoshida, T., Abe, D., & Fukuoka, Y. (2013) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/sms.12081 · Cited by 16 · see citing works

Rapid regulation of substrate use for oxidative phosphorylation during a single session of high intensity interval or aerobic exercises in different rat skeletal muscles

Martins, E. L., Ricardo, J. C., de‐Souza‐Ferreira, E., Camacho-Pereira, J., Filho, D. M. R., & Galina, A. (2017) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2017.11.013 · Cited by 13 · see citing works

Alterations to mitochondrial fatty-acid use in skeletal muscle after chronic exposure to hypoxia depend on metabolic phenotype

Malgoyre, A., Chabert, C., Tonini, J., Koulmann, N., Bigard, X. A., & Sanchez, H. (2016) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00090.2016 · Cited by 13 · see citing works

Acute myocardial ischaemia induces specific alterations of ventricular mitochondrial function in experimental pigs

Zoll, J., Ponsot, E., Doutreleau, S., Mettauer, B., Piquard, F., Mazzucotelli, J., Diemunsch, P. A., & Gény, B. (2005) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.2005.01458.x · Cited by 13 · see citing works

Alterations in mitochondrial functions and morphology in muscle and non‐muscle tissues in type 1 diabetes: implications for metabolic health

Monaco, C. M. F., Perry, C. G. R., & Hawke, T. J. (2019) · Experimental Physiology · doi:10.1113/ep088096 · Cited by 11 · see citing works

[13C]bicarbonate labelled from hyperpolarized [1-13C]pyruvate is an in vivo marker of hepatic gluconeogenesis in fasted state.

Can, E., Bastiaansen, J., Couturier, D., Rolf Gruetter, A., Yoshihara, H. A. I., & Comment, A. (2021) · Apollo (University of Cambridge) · doi:10.17863/cam.80029 · Cited by 11 · see citing works

Energy Systems: A New Look at Aerobic Metabolism in Stressful Exercise

Swanwick, E. (2018) · MOJ Sports Medicine · doi:10.15406/mojsm.2018.02.00039 · Cited by 10 · see citing works

[13C]bicarbonate labelled from hyperpolarized [1-13C]pyruvate is an in vivo marker of hepatic gluconeogenesis in fasted state

Can, E., Bastiaansen, J., Couturier, D., Gruetter, R., Yoshihara, H. A. I., & Comment, A. (2022) · Communications Biology · doi:10.1038/s42003-021-02978-2 · Cited by 10 · see citing works

Lactate is oxidized outside of the mitochondrial matrix in rodent brain

Herbst, E. A. F., George, M. A., Brebner, K., Holloway, G. P., & Kane, D. A. (2017) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2017-0450 · Cited by 9 · see citing works

Impact of dietary protein content on uncoupling protein mRNA abundance in swine

Ramsay, T. G., & Mitchell, A. D. (2007) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2007.11.007 · Cited by 9 · see citing works

Exhaustive exercise alters native and site-specific H2O2 emission in red and white skeletal muscle mitochondria

Kamunde, C., Wijayakulathilake, Y., Okoye, C. N., Chinnappareddy, N., Kalvani, Z., van den Heuvel, M., Sappal, R., & Stevens, D. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.09.018 · Cited by 7 · see citing works

Lipid metabolic features of skeletal muscle in pathological and physiological conditions

Son, Y., & Paton, C. M. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819404-1.00018-x · Cited by 7 · see citing works

Reply from Arend Bonen, Hideo Hatta, Graham P. Holloway, Lawrence L. Spriet and Yuko Yoshida

Bonen, A., Hatta, H., Holloway, G. P., Spriet, L. L., & Yoshida, Y. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.143008 · Cited by 7 · see citing works

Tissue-specific and substrate-specific mitochondrial bioenergetics in feline cardiac and skeletal muscles

Christiansen, L. B., Dela, F., Koch, J., & Yokota, T. (2015) · Journal of Veterinary Medical Science · doi:10.1292/jvms.14-0573 · Cited by 6 · see citing works

Endurance Is Improved in Female Rats After Living High-Training High Despite Alterations in Skeletal Muscle

Malgoyre, A., Prola, A., Meunier, A., Chapot, R., Serrurier, B., Koulmann, N., Bigard, X. A., & Sanchez, H. (2021) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2021.663857 · Cited by 6 · see citing works

Lactate shuttling as an allostatic means of thermoregulation in the brain

Kane, D. A., Foo, A. C. Y., Noftall, E. B., Brebner, K., & Marangoni, D. G. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1144639 · Cited by 5 · see citing works

Effects of acute cigarette smoke concentrate exposure on mitochondrial energy transfer in fast- and slow-twitch skeletal muscle

Decker, S. T., Alexandrou-Majaj, N., & Layec, G. (2023) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2023.148973 · Cited by 5 · see citing works

Mitochondria in muscle stem cell biology: gatekeepers of fate, function, and regeneration

Khacho, M., & Burelle, Y. (2026) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00027.2026 · Cited by 2 · see citing works

Energy Systems: A New Look at Aerobic Metabolism in Stressful Exercise

Swanwick, E., & Matthews, M. J. (2018) · MOJ Sports Medicine · doi:10.15406/mojsm.2017.02.00039 · Cited by 2 · see citing works

Evaluation of Mitochondrial Functions and Dysfunctions in Muscle Biopsy Samples

Capel, F., Barquissau, V., Richard, R., & Morio, B. (2012) · InTech eBooks · doi:10.5772/30705 · Cited by 1 · see citing works

Metabolic Exploration of Muscle Biopsy

Charles, A., Dufour, S. P., Chamaraux‐Tran, T., Bouitbir, J., Gény, B., & Zoll, J. (2012) · InTech eBooks · doi:10.5772/31588 · Cited by 1 · see citing works

Lactate Shuttling and the Mitochondrial Lactate Oxidation Complex

Brooks, G. A. (2012) · Oxidative stress and disease · doi:10.1201/b12308-10 · Cited by 1 · see citing works

Controle da produção muscular de espécies reativas e citocinas por ácido palmítico e eletroestimulação: possíveis implicações no envelhecimento.

Lambertucci, R. H. (2009) · doi:10.11606/t.42.2009.tde-01072009-120056 · Cited by 1 · see citing works

Effets d'un entraînement en endurance à charge constante, à charge variable ou à haute intensité chez l'homme : Etude intégrative du systémique au cellulaire

Daussin, F. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique)

B011 Stimulus specific changes of energy metabolism in hypertrophied heart

Rimbaud, S., Sanchez, H., Garnier, A., Fortin, D., Bigard, X. A., Veksler, V., & Ventura‐Clapier, R. (2009) · Archives of cardiovascular diseases · doi:10.1016/s1875-2136(09)72182-5

Tenebrio molitor (mealworm beetle) as a Model Organism for Studying Mitochondrial Physiology

Newell, C., & Kane, D. A. (2011)

Skeletal Muscle Mitochondrial Toxicity

Herbert, E. K., Herbert, S., & Herbert, K. E. (2018) · Wiley eBooks · doi:10.1002/9781119329725.ch8

Kinetic parameters of respiration in rat permeabilized hepatocytes upon Са2+ in various concentrations in medium and prolonged Influence of taurine

Merlavsky, V. M., Ostapiv, R. D., Ikkert, O. V., & Manko, V. V. (2015) · Studia Biologica · doi:10.30970/sbi.0902.439

Effect of skeletal muscle mitochondrial phenotype on H2O2 emission

Kamunde, C., Wijayakulathilake, Y., Okoye, C. N., Chinnappareddy, N., Kalvani, Z., Tetteh, P. A., van den Heuvel, M., Sappal, R., & Stevens, D. (2024) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2024.110940

Dysfonctions vasculaire et musculaire, aiguë et chronique. Quelle place pour la modulation pharmacologique du stress oxydant ?

Kremer, H. (2012) · doi:10.70675/bffabcecz39b6z4955z9446zd43bd38afbf2

Role of PGC-1β and TIF2 co-regulators in mouse skeletal muscle function

Ramamoorthy, T. G. (2013) · theses.fr (ABES) · doi:10.70675/e05002c4z4806z4363z90b1z0e406b6c0e4c

Effets de l'eau enrichie en oxygène sur l'oxygènation tissulaire : études expérimentales chez l'animal et application chez l'homme

Charton, A. (2014) · doi:10.70675/55a5d59fzb171z426az9e7ez6c6c10292950

Substrate oxidation specificity in different types of mammalian muscle

Hooker, A. M., & Baldwin, K. M. (1979) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1979.236.1.c66 · Cited by 37 · see citing works

Tissue-specific and substrate-specific mitochondrial bioenergetics in feline cardiac and skeletal muscles

Christiansen, L. B., Dela, F., Koch, J., & Yokota, T. (2015) · Journal of Veterinary Medical Science · doi:10.1292/jvms.14-0573 · Cited by 6 · see citing works

FULL PAPER Biochemistry Tissue-specific and substrate-specific mitochondrial bioenergetics in feline cardiac and skeletal muscles

Christiansen, L. B., Dela, F., Koch, J., & Yokota, T. (2014)

Oxidative capacity of muscle and mitochondria: correlation of physiological, biochemical, and morphometric characteristics.

Schwerzmann, K., Hoppeler, H. H., Kayar, S. R., & Weibel, E. R. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.5.1583 · Cited by 272 · see citing works

Oxidative capacity distribution in skeletal muscle fibers of the rat

Philippi, M. L., & Sillau, A. H. (1994) · Journal of Experimental Biology · doi:10.1242/jeb.189.1.1 · Cited by 50 · see citing works