Lactate as a myokine and exerkine: drivers and signals of physiology and metabolism
暂无分享,去创建一个
Diana D. Moreno-Santillán | Robert G. Leija | Casey C Curl | J. Arevalo | Justin J. Duong | Adam D. Osmond | George A. Brooks | Casey C. Curl | Robert G Leija | Jose A. Arevalo | Jose A Arevalo
[1] M. Cedars,et al. FULL TITLE: METABOLOMIC PROFILE OF CHILDREN CONCEIVED WITH MEDICALLY ASSISTED TECHNOLOGIES. , 2022, The Journal of clinical endocrinology and metabolism.
[2] B. Schoenfeld,et al. Beyond Mechanical Tension: A Review of Resistance Exercise-Induced Lactate Responses & Muscle Hypertrophy , 2022, Journal of functional morphology and kinesiology.
[3] Ferdinand von Meyenn,et al. H3K18 lactylation marks tissue-specific active enhancers , 2022, Genome Biology.
[4] J. Loscalzo,et al. Ultrasensitive sensors reveal the spatiotemporal landscape of lactate metabolism in physiology and disease. , 2022, Cell metabolism.
[5] A. Roldán,et al. Memory Modulation by Exercise in Young Adults Is Related to Lactate and Not Affected by Sex or BDNF Polymorphism , 2022, Biology.
[6] M. Horning,et al. Lactate as a major myokine and exerkine , 2022, Nature Reviews Endocrinology.
[7] K. Y. Loh,et al. An exercise-inducible metabolite that suppresses feeding and obesity , 2022, Nature.
[8] Christian M. Metallo,et al. The lactate-NAD+ axis activates cancer-associated fibroblasts by downregulating p62 , 2022, Cell reports.
[9] P. Brum,et al. Lactate modulates cardiac gene expression in mice during acute physical exercise , 2022, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.
[10] S. Adams,et al. Myoglobin Interaction with Lactate Rapidly Releases Oxygen: Studies on Binding Thermodynamics, Spectroscopy, and Oxygen Kinetics , 2022, International journal of molecular sciences.
[11] S. Lee,et al. Murine blastocysts generated by in vitro fertilization show increased Warburg metabolism and altered lactate production , 2022, bioRxiv.
[12] J. Botella,et al. Muscle contraction and mitochondrial biogenesis – A brief historical reappraisal , 2022, Acta physiologica.
[13] Ian R. Lanza,et al. Exerkines in health, resilience and disease , 2022, Nature Reviews Endocrinology.
[14] G. Brooks,et al. Chronic Lactate Exposure Decreases Mitochondrial Function by Inhibition of Fatty Acid Uptake and Cardiolipin Alterations in Neonatal Rat Cardiomyocytes , 2022, Frontiers in Nutrition.
[15] Zhichen Sun,et al. Lactate increases stemness of CD8 + T cells to augment anti-tumor immunity , 2021, Nature Communications.
[16] Panpan Chang,et al. Lactylated Histone H3K18 as a Potential Biomarker for the Diagnosis and Predicting the Severity of Septic Shock , 2022, Frontiers in Immunology.
[17] G. Brooks,et al. The Blood Lactate/Pyruvate Equilibrium Affair. , 2021, American journal of physiology. Endocrinology and metabolism.
[18] I. Laher,et al. The mitochondrial signaling peptide MOTS-c improves myocardial performance during exercise training in rats , 2021, Scientific reports.
[19] K. Ostrikov,et al. Histone lactylation: epigenetic mark of glycolytic switch. , 2021, Trends in genetics : TIG.
[20] Li Sun,et al. Lactate Modulates Cellular Metabolism Through Histone Lactylation-Mediated Gene Expression in Non-Small Cell Lung Cancer , 2021, Frontiers in Oncology.
[21] G. Brooks. Role of the Heart in Lactate Shuttling , 2021, Frontiers in Nutrition.
[22] G. Brooks,et al. Lactate in contemporary biology: a phoenix risen , 2021, The Journal of physiology.
[23] R. Bellomo,et al. The importance of applying physiological principles of hyperlactataemia to the study of human disease , 2021, The Journal of physiology.
[24] B. Benayoun,et al. MOTS-c is an exercise-induced mitochondrial-encoded regulator of age-dependent physical decline and muscle homeostasis , 2021, Nature Communications.
[25] C. Moinpour,et al. Association of Osteonecrosis of the Jaw With Zoledronic Acid Treatment for Bone Metastases in Patients With Cancer. , 2020, JAMA oncology.
[26] D. Mougiakakos,et al. Metabolic reprogramming of osteoclasts represents a therapeutic target during the treatment of osteoporosis , 2020, Scientific Reports.
[27] G. Brooks,et al. The anaerobic threshold: 50+ years of controversy , 2020, The Journal of physiology.
[28] M. Sharpley,et al. Metabolic Plasticity drives Development during Mammalian Embryogenesis , 2020, bioRxiv.
[29] T. Hazell,et al. The emerging role of lactate as a mediator of exercise-induced appetite suppression. , 2020, American journal of physiology. Endocrinology and metabolism.
[30] J. Rabinowitz,et al. Lactate: the ugly duckling of energy metabolism , 2020, Nature Metabolism.
[31] M. Pohanka. D-Lactic Acid as a Metabolite: Toxicology, Diagnosis, and Detection , 2020, BioMed research international.
[32] P. Tso,et al. Glucagon like peptide 1 and glucose-dependent insulinotropic polypeptide stimulate the release of substance P from TRPV1 and TRPA1 expressing sensory nerves. , 2020, American journal of physiology. Gastrointestinal and liver physiology.
[33] Greg L. McKie,et al. Greater lactate accumulation following an acute bout of high-intensity exercise in males suppresses acylated ghrelin and appetite post-exercise. , 2020, Journal of applied physiology.
[34] G. Brooks. Lactate as a fulcrum of metabolism , 2020, Redox biology.
[35] D. Poole,et al. The role of vascular function on exercise capacity in health and disease , 2020, The Journal of physiology.
[36] R. Deberardinis,et al. Assessment of Rapid Hepatic Glycogen Synthesis in Humans Using Dynamic 13C Magnetic Resonance Spectroscopy , 2020, Hepatology communications.
[37] G. Brooks,et al. Is Lactate an Oncometabolite? Evidence Supporting a Role for Lactate in the Regulation of Transcriptional Activity of Cancer-Related Genes in MCF7 Breast Cancer Cells , 2020, Frontiers in Oncology.
[38] M. Ruscica,et al. Lactate Buildup at the Site of Chronic Inflammation Promotes Disease by Inducing CD4+ T Cell Metabolic Rewiring , 2019, Cell metabolism.
[39] Alexander V. Zhdanov,et al. Short‐chain fatty acids and microbiota metabolites attenuate ghrelin receptor signaling , 2019, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[40] B. Ren,et al. Metabolic regulation of gene expression by histone lactylation , 2019, Nature.
[41] D. Bishop,et al. A physiological drop in pH decreases mitochondrial respiration, and HDAC and Akt signaling, in L6 myocytes. , 2019, American journal of physiology. Cell physiology.
[42] T. Clanton. Managing the power grid: how myoglobin can regulate PO2 and energy distribution in skeletal muscle. , 2019, Journal of applied physiology.
[43] Sama F. Sleiman,et al. Lactate Mediates the Effects of Exercise on Learning and Memory through SIRT1-Dependent Activation of Hippocampal Brain-Derived Neurotrophic Factor (BDNF) , 2019, The Journal of Neuroscience.
[44] W. Thompson,et al. Sarcopenia: Aging-Related Loss of Muscle Mass and Function. , 2019, Physiological reviews.
[45] W. Kraus,et al. The Scientific Foundation for the Physical Activity Guidelines for Americans, 2nd Edition. , 2019, Journal of physical activity & health.
[46] Xiaofei Li,et al. Lactate dehydrogenase A: A key player in carcinogenesis and potential target in cancer therapy , 2018, Cancer medicine.
[47] P. Magistretti,et al. L-Lactate Regulates the Expression of Synaptic Plasticity and Neuroprotection Genes in Cortical Neurons: A Transcriptome Analysis , 2018, Front. Mol. Neurosci..
[48] B. Benayoun,et al. The Mitochondrial-Encoded Peptide MOTS-c Translocates to the Nucleus to Regulate Nuclear Gene Expression in Response to Metabolic Stress. , 2018, Cell metabolism.
[49] G. Brooks. The Science and Translation of Lactate Shuttle Theory. , 2018, Cell metabolism.
[50] T. Schwartz,et al. Enterochromaffin 5-HT cells – A major target for GLP-1 and gut microbial metabolites , 2018, Molecular metabolism.
[51] A. Figueroa,et al. Aerobic training but no resistance training increases SIRT3 in skeletal muscle of sedentary obese male adolescents , 2018, European journal of sport science.
[52] N. Secher,et al. Maintained exercise‐enhanced brain executive function related to cerebral lactate metabolism in men , 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[53] G. Brooks,et al. Assessment of Metabolic Flexibility by Means of Measuring Blood Lactate, Fat, and Carbohydrate Oxidation Responses to Exercise in Professional Endurance Athletes and Less-Fit Individuals , 2018, Sports Medicine.
[54] L. Gladden,et al. Lactate metabolism: historical context, prior misinterpretations, and current understanding , 2018, European Journal of Applied Physiology.
[55] Joshua D. Rabinowitz,et al. Glucose feeds the TCA cycle via circulating lactate , 2017, Nature.
[56] Greg L. McKie,et al. Potential involvement of lactate and interleukin-6 in the appetite-regulatory hormonal response to an acute exercise bout , 2017, Journal of applied physiology.
[57] M. Sharpley,et al. Nuclear Localization of Mitochondrial TCA Cycle Enzymes as a Critical Step in Mammalian Zygotic Genome Activation , 2017, Cell.
[58] G. Brooks,et al. Reexamining cancer metabolism: lactate production for carcinogenesis could be the purpose and explanation of the Warburg Effect , 2016, Carcinogenesis.
[59] Minas Nalbandian,et al. Lactate as a Signaling Molecule That Regulates Exercise-Induced Adaptations , 2016, Biology.
[60] Stephen L. Johnson,et al. Lactate Metabolism is Associated with Mammalian Mitochondria , 2016, Nature chemical biology.
[61] R. Meuli,et al. Improvement of Neuroenergetics by Hypertonic Lactate Therapy in Patients with Traumatic Brain Injury Is Dependent on Baseline Cerebral Lactate/Pyruvate Ratio , 2016, Journal of neurotrauma.
[62] P. Marik,et al. A rational approach to fluid therapy in sepsis. , 2016, British journal of anaesthesia.
[63] B. Faubert,et al. Metabolic Heterogeneity in Human Lung Tumors , 2016, Cell.
[64] Karl R. Clauser,et al. MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins , 2015, Nucleic Acids Res..
[65] M. Krasnow,et al. Oxygen regulation of breathing through an olfactory receptor activated by lactate , 2016 .
[66] M. Lindholm,et al. Skeletal muscle hypoxia‐inducible factor‐1 and exercise , 2008, Experimental physiology.
[67] S. Feuer,et al. Common and specific transcriptional signatures in mouse embryos and adult tissues induced by in vitro procedures. , 2016, Reproduction.
[68] T. Takemasa,et al. High-intensity interval training-induced metabolic adaptation coupled with an increase in Hif-1α and glycolytic protein expression. , 2015, Journal of applied physiology.
[69] Daisuke Hoshino,et al. Effects of decreased lactate accumulation after dichloroacetate administration on exercise training–induced mitochondrial adaptations in mouse skeletal muscle , 2015, Physiological reports.
[70] Sriram Subramaniam,et al. Mitochondrial reticulum for cellular energy distribution in muscle , 2015, Nature.
[71] F. D’Acquisto,et al. Lactate Regulates Metabolic and Pro-inflammatory Circuits in Control of T Cell Migration and Effector Functions , 2015, PLoS biology.
[72] G. Brooks,et al. Endogenous Nutritive Support after Traumatic Brain Injury: Peripheral Lactate Production for Glucose Supply via Gluconeogenesis , 2015, Journal of neurotrauma.
[73] Michael A. Horning,et al. Lactate: Brain Fuel in Human Traumatic Brain Injury: A Comparison with Normal Healthy Control Subjects , 2015, Journal of neurotrauma.
[74] W. Zhan,et al. Oxamate-mediated inhibition of lactate dehydrogenase induces protective autophagy in gastric cancer cells: involvement of the Akt-mTOR signaling pathway. , 2015, Cancer letters.
[75] G. Rutter,et al. Pancreatic β-cell identity, glucose sensing and the control of insulin secretion. , 2015, The Biochemical journal.
[76] L. Bruce Gladden,et al. Lactate is always the end product of glycolysis , 2015, Front. Neurosci..
[77] G. Brooks,et al. Cerebral metabolism following traumatic brain injury: new discoveries with implications for treatment , 2015, Front. Neurosci..
[78] L. Bergersen. Lactate Transport and Signaling in the Brain: Potential Therapeutic Targets and Roles in Body—Brain Interaction , 2015, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[79] M. Tan,et al. The Warburg effect in tumor progression: mitochondrial oxidative metabolism as an anti-metastasis mechanism. , 2015, Cancer letters.
[80] Kevin B. Jones,et al. Lactate and Cancer: Revisiting the Warburg Effect in an Era of Lactate Shuttling , 2015, Front. Nutr..
[81] Albert Gjedde,et al. Lactate receptor sites link neurotransmission, neurovascular coupling, and brain energy metabolism. , 2014, Cerebral cortex.
[82] P. Marik,et al. Sepsis-associated hyperlactatemia , 2014, Critical Care.
[83] Pascal Jourdain,et al. Lactate promotes plasticity gene expression by potentiating NMDA signaling in neurons , 2014, Proceedings of the National Academy of Sciences.
[84] V. Giusti,et al. Metabolic Fate of Fructose Ingested with and without Glucose in a Mixed Meal , 2014, Nutrients.
[85] Asan,et al. Altitude adaptation in Tibet caused by introgression of Denisovan-like DNA , 2014, Nature.
[86] R. Hoque,et al. Lactate reduces liver and pancreatic injury in Toll-like receptor- and inflammasome-mediated inflammation via GPR81-mediated suppression of innate immunity. , 2014, Gastroenterology.
[87] Han Xie,et al. Targeting lactate dehydrogenase--a inhibits tumorigenesis and tumor progression in mouse models of lung cancer and impacts tumor-initiating cells. , 2014, Cell metabolism.
[88] W. Bloch,et al. Lactate regulates myogenesis in C2C12 myoblasts in vitro. , 2014, Stem cell research.
[89] E. Seront,et al. Antitumor Activity of 7-Aminocarboxycoumarin Derivatives, a New Class of Potent Inhibitors of Lactate Influx but Not Efflux , 2014, Molecular Cancer Therapeutics.
[90] Mark A. Hall,et al. Blocking lactate export by inhibiting the Myc target MCT1 Disables glycolysis and glutathione synthesis. , 2014, Cancer research.
[91] Reto Meuli,et al. Cerebral metabolic effects of exogenous lactate supplementation on the injured human brain , 2014, Intensive Care Medicine.
[92] Xiaoguang Sun,et al. Lactate dehydrogenase a in cancer: A promising target for diagnosis and therapy , 2013, IUBMB life.
[93] J. Herman,et al. Role of central glucagon-like peptide-1 in stress regulation , 2013, Physiology & Behavior.
[94] John L Cleveland,et al. Targeting lactate metabolism for cancer therapeutics. , 2013, Journal of Clinical Investigation.
[95] T. Clanton,et al. Regulation of cellular gas exchange, oxygen sensing, and metabolic control. , 2013, Comprehensive Physiology.
[96] Chi-An W. Emhoff,et al. Lactate kinetics at the lactate threshold in trained and untrained men. , 2013, Journal of applied physiology.
[97] Carsten Lundby,et al. Lactate oxidation in human skeletal muscle mitochondria. , 2013, American journal of physiology. Endocrinology and metabolism.
[98] Chi-An W. Emhoff,et al. Gluconeogenesis and hepatic glycogenolysis during exercise at the lactate threshold , 2013, Journal of applied physiology.
[99] J. Verrax,et al. Lactate Activates HIF-1 in Oxidative but Not in Warburg-Phenotype Human Tumor Cells , 2012, PloS one.
[100] E. Zoetendal,et al. Transfer of intestinal microbiota from lean donors increases insulin sensitivity in individuals with metabolic syndrome. , 2012, Gastroenterology.
[101] Gang Huang,et al. Knockdown of lactate dehydrogenase A suppresses tumor growth and metastasis of human hepatocellular carcinoma , 2012, The FEBS journal.
[102] D. Sabatini,et al. Cancer cell metabolism: one hallmark, many faces. , 2012, Cancer discovery.
[103] N. Secher,et al. Hypoxia and exercise provoke both lactate release and lactate oxidation by the human brain , 2012, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[104] M. Hallschmid,et al. Lactate infusion during euglycemia but not hypoglycemia reduces subsequent food intake in healthy men , 2012, Appetite.
[105] P. Magistretti,et al. Brain Lactate Metabolism in Humans With Subarachnoid Hemorrhage , 2012, Stroke.
[106] N. Goplen,et al. The role of low-level lactate production in airway inflammation in asthma. , 2012, American journal of physiology. Lung cellular and molecular physiology.
[107] Chi-An W. Emhoff,et al. Transpulmonary lactate shuttle. , 2012, American journal of physiology. Regulatory, integrative and comparative physiology.
[108] O. Feron,et al. Lactate shuttles at a glance: from physiological paradigms to anti-cancer treatments , 2011, Disease Models & Mechanisms.
[109] Bechien U. Wu,et al. Lactated Ringer's solution reduces systemic inflammation compared with saline in patients with acute pancreatitis. , 2011, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[110] B. Spiegelman,et al. PGC-1 coactivators and the regulation of skeletal muscle fiber-type determination. , 2011, Cell metabolism.
[111] G. Brooks,et al. Mitochondrial and plasma membrane lactate transporter and lactate dehydrogenase isoform expression in breast cancer cell lines. , 2011, Physiological genomics.
[112] B. Sperlich,et al. Lactate infusion at rest increases BDNF blood concentration in humans , 2011, Neuroscience Letters.
[113] E. Negelein,et al. THE METABOLISM OF CARCINOMA CELLS , 2011 .
[114] G. Semenza. Regulation of metabolism by hypoxia-inducible factor 1. , 2011, Cold Spring Harbor symposia on quantitative biology.
[115] G. Millet,et al. Fructose and glucose co-ingestion during prolonged exercise increases lactate and glucose fluxes and oxidation compared with an equimolar intake of glucose. , 2010, The American journal of clinical nutrition.
[116] K. Petersen,et al. The Contribution of Blood Lactate to Brain Energy Metabolism in Humans Measured by Dynamic 13C Nuclear Magnetic Resonance Spectroscopy , 2010, The Journal of Neuroscience.
[117] T. Iwanaga,et al. The cellular expression of SMCT2 and its comparison with other transporters for monocarboxylates in the mouse digestive tract. , 2010, Biomedical research.
[118] S. Tunaru,et al. An autocrine lactate loop mediates insulin-dependent inhibition of lipolysis through GPR81. , 2010, Cell metabolism.
[119] M. Kaufman. Metaboreflex control of the heart , 2010, The Journal of physiology.
[120] G. Rutter,et al. Identification of genes selectively disallowed in the pancreatic islet , 2010, Islets.
[121] G. Semenza. HIF-1: upstream and downstream of cancer metabolism. , 2010, Current opinion in genetics & development.
[122] A. Halestrap,et al. AR-C155858 is a potent inhibitor of monocarboxylate transporters MCT1 and MCT2 that binds to an intracellular site involving transmembrane helices 7–10 , 2009, The Biochemical journal.
[123] G. Brooks,et al. Cell–cell and intracellular lactate shuttles , 2009, The Journal of physiology.
[124] G. Brooks,et al. Effects of endurance training on cardiorespiratory fitness and substrate partitioning in postmenopausal women. , 2009, Metabolism: clinical and experimental.
[125] F. Oswald,et al. CD147 silencing inhibits lactate transport and reduces malignant potential of pancreatic cancer cells in in vivo and in vitro models , 2009, Gut.
[126] Xiang Chen,et al. A CD147-targeting siRNA inhibits the proliferation, invasiveness, and VEGF production of human malignant melanoma cells by down-regulating glycolysis. , 2009, Cancer letters.
[127] J. Born,et al. Lactate overrides central nervous but not beta-cell glucose sensing in humans. , 2008, Metabolism: clinical and experimental.
[128] Julien Verrax,et al. Targeting lactate-fueled respiration selectively kills hypoxic tumor cells in mice. , 2008, The Journal of clinical investigation.
[129] G. Semenza,et al. Uterine DCs are essential for pregnancy. , 2008, The Journal of clinical investigation.
[130] M. Febbraio,et al. Muscle as an endocrine organ: focus on muscle-derived interleukin-6. , 2008, Physiological reviews.
[131] M. Inoue,et al. Blocking CD147 induces cell death in cancer cells through impairment of glycolytic energy metabolism. , 2008, Biochemical and biophysical research communications.
[132] A. Bonen,et al. PGC-1alpha increases skeletal muscle lactate uptake by increasing the expression of MCT1 but not MCT2 or MCT4. , 2008, Physiological genomics.
[133] S. Carr,et al. A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology , 2008, Cell.
[134] G. Brooks,et al. Glucoregulation is more precise in women than in men during postexercise recovery. , 2008, The American journal of clinical nutrition.
[135] T. K. Hunt,et al. Lactate, with oxygen, incites angiogenesis. , 2008, Advances in experimental medicine and biology.
[136] G. Brooks,et al. Lipolysis and fatty acid metabolism in men and women during the postexercise recovery period , 2007, The Journal of physiology.
[137] R. Knight,et al. The Human Microbiome Project , 2007, Nature.
[138] J. Azevedo,et al. Lactate, Fructose and Glucose Oxidation Profiles in Sports Drinks and the Effect on Exercise Performance , 2007, PloS one.
[139] J. Kere,et al. Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells. , 2007, American journal of human genetics.
[140] George A. Brooks,et al. Lactate sensitive transcription factor network in L6 cells: activation of MCT1 and mitochondrial biogenesis , 2007, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[141] T. K. Hunt,et al. Aerobically derived lactate stimulates revascularization and tissue repair via redox mechanisms. , 2007, Antioxidants & redox signaling.
[142] Hong Yang,et al. Inhibition of CD147 gene expression via RNA interference reduces tumor cell invasion, tumorigenicity and increases chemosensitivity to paclitaxel in HO-8910pm cells. , 2007, Cancer letters.
[143] P. Major,et al. Hypoxia-induced lactate dehydrogenase expression and tumor angiogenesis. , 2007, Clinical colorectal cancer.
[144] G. Brooks,et al. Pyruvate metabolism in working human skeletal muscle. , 2006, American journal of physiology. Endocrinology and metabolism.
[145] S. Bloom,et al. Gut hormones and the regulation of energy homeostasis , 2006, Nature.
[146] H. Pilegaard,et al. Control of gene expression and mitochondrial biogenesis in the muscular adaptation to endurance exercise. , 2006, Essays in biochemistry.
[147] L. Brennan,et al. The importance of redox shuttles to pancreatic beta-cell energy metabolism and function. , 2006, Biochemical Society transactions.
[148] G. Brooks,et al. Colocalization of MCT1, CD147, and LDH in mitochondrial inner membrane of L6 muscle cells: evidence of a mitochondrial lactate oxidation complex. , 2006, American journal of physiology. Endocrinology and metabolism.
[149] G. Semenza,et al. HIF-1-mediated expression of pyruvate dehydrogenase kinase: a metabolic switch required for cellular adaptation to hypoxia. , 2006, Cell metabolism.
[150] D. Hardie,et al. AMPK: a key sensor of fuel and energy status in skeletal muscle. , 2006, Physiology.
[151] Avital Schurr,et al. Lactate: The Ultimate Cerebral Oxidative Energy Substrate? , 2006, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[152] M. Gassmann,et al. Regular endurance training reduces the exercise induced HIF-1alpha and HIF-2alpha mRNA expression in human skeletal muscle in normoxic conditions. , 2006, European journal of applied physiology.
[153] G. Brooks,et al. Immunohistochemical analysis of MCT1, MCT2 and MCT4 expression in rat plantaris muscle , 2005, The Journal of physiology.
[154] D. Gardner,et al. Mitochondrial Malate-Aspartate Shuttle Regulates Mouse Embryo Nutrient Consumption* , 2005, Journal of Biological Chemistry.
[155] G. Brooks,et al. Hematological and acid-base changes in men during prolonged exercise with and without sodium-lactate infusion. , 2005, Journal of applied physiology.
[156] O. Warburg,et al. Versuche an Überlebendem Carcinomgewebe , 1923, Klinische Wochenschrift.
[157] H. T. Yang,et al. What makes vessels grow with exercise training? , 2004, Journal of applied physiology.
[158] G. Brooks,et al. MCT1 confirmed in rat striated muscle mitochondria. , 2004, Journal of applied physiology.
[159] L. Gladden. Lactate metabolism: a new paradigm for the third millennium , 2004, The Journal of physiology.
[160] G. Brooks,et al. Pyruvate shuttling during rest and exercise before and after endurance training in men. , 2004, Journal of applied physiology.
[161] M. Romero,et al. The human tumour suppressor gene SLC5A8 expresses a Na+–monocarboxylate cotransporter , 2004, The Journal of physiology.
[162] C. Mantzoros,et al. Energy homeostasis, obesity and eating disorders: recent advances in endocrinology. , 2004, The Journal of nutrition.
[163] J. Keul,et al. The significance of the aerobic-anaerobic transition for the determination of work load intensities during endurance training , 1979, European Journal of Applied Physiology and Occupational Physiology.
[164] S. Welle,et al. Pathways for glucose disposal after meal ingestion in humans. , 2003, American journal of physiology. Endocrinology and metabolism.
[165] G. Shulman,et al. Local lactate perfusion of the ventromedial hypothalamus suppresses hypoglycemic counterregulation. , 2003, Diabetes.
[166] G. Brooks,et al. Lactate and glucose interactions during rest and exercise in men: effect of exogenous lactate infusion , 2002, The Journal of physiology.
[167] C. Cotman,et al. Exercise: a behavioral intervention to enhance brain health and plasticity , 2002, Trends in Neurosciences.
[168] G. Brooks. Lactate shuttle – between but not within cells? , 2002, The Journal of physiology.
[169] M. Stumvoll,et al. Renal substrate exchange and gluconeogenesis in normal postabsorptive humans. , 2002, American journal of physiology. Endocrinology and metabolism.
[170] S. Welle,et al. Role of human liver, kidney, and skeletal muscle in postprandial glucose homeostasis. , 2002, American journal of physiology. Endocrinology and metabolism.
[171] G. Brooks,et al. Lactate shuttles in nature. , 2001, Biochemical Society transactions.
[172] A. Hingorani,et al. D-lactate encephalopathy , 2001, The Lancet.
[173] P. S. Wang,et al. Stimulatory effect of lactate on testosterone production by rat Leydig cells , 2001, Journal of cellular biochemistry.
[174] M. Stumvoll,et al. Renal gluconeogenesis: its importance in human glucose homeostasis. , 2001, Diabetes care.
[175] G. Brooks,et al. Endurance training, expression, and physiology of LDH, MCT1, and MCT4 in human skeletal muscle. , 2000, American journal of physiology. Endocrinology and metabolism.
[176] G. Brooks,et al. Endurance training increases gluconeogenesis during rest and exercise in men. , 2000, American journal of physiology. Endocrinology and metabolism.
[177] S. Matsugo,et al. The lactate-dependent enhancement of hydroxyl radical generation by the Fenton reaction , 2000, Free radical research.
[178] G. Brooks,et al. Active muscle and whole body lactate kinetics after endurance training in men. , 1999, Journal of applied physiology.
[179] G. Brooks,et al. Cardiac and skeletal muscle mitochondria have a monocarboxylate transporter MCT1. , 1999, Journal of applied physiology.
[180] V. Mootha,et al. Mechanisms Controlling Mitochondrial Biogenesis and Respiration through the Thermogenic Coactivator PGC-1 , 1999, Cell.
[181] S. Powers,et al. Exercise training-induced alterations in skeletal muscle antioxidant capacity: a brief review. , 1999, Medicine and science in sports and exercise.
[182] G. Brooks,et al. Endurance training increases fatty acid turnover, but not fat oxidation, in young men. , 1999, Journal of applied physiology.
[183] H. Pilegaard,et al. Distribution of the lactate/H+ transporter isoforms MCT1 and MCT4 in human skeletal muscle. , 1999, American journal of physiology. Endocrinology and metabolism.
[184] G. Brooks,et al. Role of mitochondrial lactate dehydrogenase and lactate oxidation in the intracellular lactate shuttle. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[185] G. Brooks,et al. Effects of exercise intensity and training on lipid metabolism in young women. , 1998, American journal of physiology. Endocrinology and metabolism.
[186] P. Magistretti,et al. Evidence Supporting the Existence of an Activity-Dependent Astrocyte-Neuron Lactate Shuttle , 1998, Developmental Neuroscience.
[187] G. Brooks,et al. Training-induced alterations of carbohydrate metabolism in women: women respond differently from men. , 1998, Journal of applied physiology.
[188] G. Brooks,et al. Mammalian fuel utilization during sustained exercise. , 1998, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.
[189] N. Price,et al. Cloning and sequencing of four new mammalian monocarboxylate transporter (MCT) homologues confirms the existence of a transporter family with an ancient past. , 1998, The Biochemical journal.
[190] P. S. Wang,et al. Lactate and the effects of exercise on testosterone secretion: evidence for the involvement of a cAMP-mediated mechanism. , 1997, Medicine and science in sports and exercise.
[191] G. Brooks,et al. Training-induced alterations of glucose flux in men. , 1997, Journal of applied physiology.
[192] A. R. Jones,et al. Metabolism of lactate by mature boar spermatozoa. , 1997, Reproduction, fertility, and development.
[193] P. W. Hochachka,et al. Unifying theory of hypoxia tolerance: molecular/metabolic defense and rescue mechanisms for surviving oxygen lack. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[194] P. Magistretti,et al. Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[195] G. Brooks,et al. Trans-stimulation of lactate transport from rat sarcolemmal membrane vesicles. , 1994, Archives of biochemistry and biophysics.
[196] G. Brooks,et al. Balance of carbohydrate and lipid utilization during exercise: the "crossover" concept. , 1994, Journal of applied physiology.
[197] Richard G. W. Anderson,et al. Molecular characterization of a membrane transporter for lactate, pyruvate, and other monocarboxylates: Implications for the Cori cycle , 1994, Cell.
[198] L. Witters,et al. Acetyl-CoA carboxylase regulation of fatty acid oxidation in the heart. , 1993, The Journal of biological chemistry.
[199] D. O'Leary. Autonomic mechanisms of muscle metaboreflex control of heart rate. , 1993, Journal of applied physiology.
[200] R. Knazek,et al. Oral gossypol in the treatment of metastatic adrenal cancer. , 1993, The Journal of clinical endocrinology and metabolism.
[201] B. Saltin,et al. Lactate and H+ effluxes from human skeletal muscles during intense, dynamic exercise. , 1993, The Journal of physiology.
[202] G. Semenza,et al. A nuclear factor induced by hypoxia via de novo protein synthesis binds to the human erythropoietin gene enhancer at a site required for transcriptional activation , 1992, Molecular and cellular biology.
[203] L. Mandarino,et al. Skeletal muscle is a major site of lactate uptake and release during hyperinsulinemia. , 1992, Metabolism: clinical and experimental.
[204] D. Whittingham,et al. The roles of pyruvate, lactate and glucose during preimplantation development of embryos from F1 hybrid mice in vitro. , 1991, Development.
[205] J. Wisneski,et al. Myocardial substrate utilization during exercise in humans. Dual carbon-labeled carbohydrate isotope experiments. , 1988, The Journal of clinical investigation.
[206] A. Schurr,et al. Lactate-supported synaptic function in the rat hippocampal slice preparation. , 1988, Science.
[207] P. Ferré,et al. Metabolic fate of a gastric glucose load in unrestrained rats bearing a portal vein catheter. , 1988, The American journal of physiology.
[208] G. Brooks,et al. Effects of endurance training on a mitochondrial reticulum in limb skeletal muscle. , 1987, Archives of biochemistry and biophysics.
[209] G. Brooks. Lactate production under fully aerobic conditions: the lactate shuttle during rest and exercise. , 1986, Federation proceedings.
[210] D. James,et al. Intrinsic differences of insulin receptor kinase activity in red and white muscle. , 1986, The Journal of biological chemistry.
[211] G. Brooks,et al. Mitochondrial reticulum in limb skeletal muscle. , 1986, The American journal of physiology.
[212] C. Willíams,et al. Human muscle metabolism during sprint running. , 1986, Journal of applied physiology.
[213] G. Brooks,et al. Lactate extraction during net lactate release in legs of humans during exercise. , 1986, Journal of applied physiology.
[214] D. James,et al. Effects of exercise training on in vivo insulin action in individual tissues of the rat. , 1985, The Journal of clinical investigation.
[215] G. Brooks,et al. Systemic lactate kinetics during graded exercise in man. , 1985, The American journal of physiology.
[216] G. Brooks,et al. Anaerobic threshold: review of the concept and directions for future research. , 1985, Medicine and science in sports and exercise.
[217] G. Brooks. Lactate:Glycolytic End Product and Oxidative Substrate During Sustained Exercise in Mammals — The “Lactate Shuttle” , 1985 .
[218] D. W. Foster. From Glycogen to Ketones—And Back , 1984, Diabetes.
[219] D. Wasserman,et al. Interactions between glucagon and other counterregulatory hormones during normoglycemic and hypoglycemic exercise in dogs. , 1984, The Journal of clinical investigation.
[220] E. Coyle,et al. Adaptations of skeletal muscle to endurance exercise and their metabolic consequences. , 1984, Journal of applied physiology: respiratory, environmental and exercise physiology.
[221] G. Brooks,et al. Exercise physiology: Human bioenergetics and its applications , 1984 .
[222] G. Brooks,et al. Effect of endurance training on glucose kinetics during exercise. , 1983, The American journal of physiology.
[223] R. Armstrong,et al. Is Lactic Acid Related to Delayed-Onset Muscle Soreness? , 1983, The Physician and sportsmedicine.
[224] G. Brooks,et al. Endurance training affects lactate clearance, not lactate production. , 1983, The American journal of physiology.
[225] D. Schoeller,et al. Pulse injection, 13C tracer studies of lactate metabolism in humans during rest and two levels of exercise. , 1982, Biomedical mass spectrometry.
[226] G. Brooks,et al. Biochemical adaptation of mitochondria, muscle, and whole-animal respiration to endurance training. , 1981, Archives of biochemistry and biophysics.
[227] J. Bristow,et al. Myocardial Lactate Metabolism: Evidence of Lactate Release During Net Chemical Extraction in Man , 1981, Circulation.
[228] K. Baldwin,et al. Substrate oxidation specificity in different types of mammalian muscle. , 1979, The American journal of physiology.
[229] P. Campbell,et al. Glycogen, lactate, and alanine changes in muscle fiber types during graded exercise. , 1977, Journal of applied physiology: respiratory, environmental and exercise physiology.
[230] K. Sahlin,et al. Lactate content and pH in muscle obtained after dynamic exercise. , 1976, Pflugers Archiv : European journal of physiology.
[231] E. Hultman,et al. Liver and muscle glycogen in man after glucose and fructose infusion. , 1974, Scandinavian journal of clinical and laboratory investigation.
[232] E. Racker. Bioenergetics and the problem of tumor growth. , 1972, American scientist.
[233] J. A. Johnson,et al. The role of the skin in carbohydrate metabolism. , 1972, Advances in metabolic disorders.
[234] V. Edgerton,et al. Histochemical, biochemical, and contractile properties of red, white, and intermediate fibers. , 1971, The American journal of physiology.
[235] V. Edgerton,et al. Effect of exercise on skeletal muscle. I. Biochemical and histochemical properties. , 1970, Journal of applied physiology.
[236] W. Stainsby,et al. Oxygen debt in contracting dog skeletal muscle in situ. , 1967, Respiration physiology.
[237] J. Holloszy. Biochemical adaptations in muscle. Effects of exercise on mitochondrial oxygen uptake and respiratory enzyme activity in skeletal muscle. , 1967, The Journal of biological chemistry.
[238] C. Gisolfi,et al. Effects of aerobic work performed during recovery from exhausting work. , 1966, Journal of applied physiology.
[239] E. Neufeld,et al. CARBOHYDRATE METABOLISM. , 1965, Annual review of biochemistry.
[240] K. Wasserman,et al. DETECTING THE THRESHOLD OF ANAEROBIC METABOLISM IN CARDIAC PATIENTS DURING EXERCISE. , 1964, The American journal of cardiology.
[241] S. Colowick,et al. The role of glycolysis in the growth of tumor cells. I. Effects of oxamic acid on the metabolism of Ehrlich ascites tumor cells in vitro. , 1961, The Journal of biological chemistry.
[242] R. Margaria,et al. THE POSSIBLE MECHANISMS OF CONTRACTING AND PAYING THE OXYGEN DEBT AND THE RÔLE OF LACTIC ACID IN MUSCULAR CONTRACTION , 1933 .
[243] C. N. H. Long,et al. Muscular exercise, lactic acid, and the supply and utilisation of oxygen , 1924 .