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Endocrinology, ISSN 0013-7227, 03/2005, Volume 146, Issue 3, pp. 1328 - 1337
Journal Article
Circulation Research: Journal of the American Heart Association, ISSN 0009-7330, 06/2001, Volume 88, Issue 12, pp. 1276 - 1282
Itis generally accepted that endothelial cells generate most of their ATP byanaerobic glycolysis and that very little ATP is derived from the oxidation offatty... 
AICAR | Fuel metabolism | Acetyl CoA carboxylase | Glucose transport | Malonyl CoA | glucose transport | malonyl CoA | CARDIAC & CARDIOVASCULAR SYSTEMS | fuel metabolism | NITRIC-OXIDE SYNTHASE | OLEIC-ACID | ACETYL-COA CARBOXYLASE | VASCULAR ENDOTHELIUM | SKELETAL-MUSCLE | acetyl CoA carboxylase | METABOLISM | MALONYL-COA | GLUCOSE | PERIPHERAL VASCULAR DISEASE | NO SYNTHASE | HEMATOLOGY | CEREBRAL MICROVESSELS | Endothelium, Vascular - cytology | Palmitic Acid - metabolism | Humans | Multienzyme Complexes - metabolism | Endothelium, Vascular - drug effects | Tritium | Carnitine - metabolism | Caprylates - metabolism | Glycolysis - drug effects | AMP-Activated Protein Kinases | Aminoimidazole Carboxamide - pharmacology | Dose-Response Relationship, Drug | Ribonucleotides - pharmacology | Malonyl Coenzyme A - metabolism | Carnitine - pharmacology | Adenosine Triphosphate - metabolism | Oxidation-Reduction - drug effects | Aminoimidazole Carboxamide - metabolism | Energy Metabolism - physiology | Fatty Acids - metabolism | 3-O-Methylglucose - pharmacokinetics | Intracellular Fluid - metabolism | Protein-Serine-Threonine Kinases - metabolism | Ribonucleotides - metabolism | Cells, Cultured | Umbilical Veins | Glucose - pharmacology | Enzyme Activation - drug effects | Aminoimidazole Carboxamide - analogs & derivatives | Endothelium, Vascular - metabolism | Glucose - pharmacokinetics | Glucose - metabolism | Acetyl-CoA Carboxylase - metabolism | Energy Metabolism - drug effects
Journal Article
Journal Article
Journal Article
Biochemical Journal, ISSN 0264-6021, 03/2005, Volume 386, Issue 3, pp. 471 - 478
Journal Article
Animal Reproduction Science, ISSN 0378-4320, 07/2016, Volume 170, pp. 157 - 169
Journal Article
Cardiology, ISSN 0008-6312, 04/2015, Volume 130, Issue 4, pp. 211 - 220
When subjected to pressure overload, the ventricular myocardium shifts from fatty acids to glucose as its main source for energy provision and frequently... 
Review | 2-deoxy-2- | Mechanistic target of rapamycin activation | Glucose 6-phosphate | F]fluoro-D-glucose positron emission tomography | Left ventricular hypertrophy | Endoplasmic reticulum stress | CARDIAC & CARDIOVASCULAR SYSTEMS | SPONTANEOUSLY HYPERTENSIVE-RAT | PET IMAGES | DILATED CARDIOMYOPATHY | OXIDATIVE-METABOLISM | POSITRON-EMISSION-TOMOGRAPHY | RESONANCE-SPECTROSCOPY | MYOCARDIAL FATTY-ACID | CARDIAC-HYPERTROPHY | INPUT FUNCTION | 2-deoxy-2-[F-18] fluoro-D-glucose positron emission tomography Glucose 6-phosphate | CONGESTIVE-HEART-FAILURE | Hypoglycemic Agents - therapeutic use | 3-O-Methylglucose - metabolism | Sirolimus - therapeutic use | Metformin - therapeutic use | TOR Serine-Threonine Kinases - metabolism | Ventricular Function, Left | Humans | Heart Failure - physiopathology | Rats | Positron-Emission Tomography | 3-O-Methylglucose - analogs & derivatives | Hypertrophy, Left Ventricular - therapy | Animals | Myocardium - metabolism | Hypertension - complications | Heart Ventricles - metabolism | Mice | Hypertrophy, Left Ventricular - physiopathology | Fatty Acids - metabolism | Glucose-6-Phosphate - metabolism | Disease Models, Animal | Endoplasmic Reticulum Stress - physiology | Metabolism | Enzymes | Glucose | Left Ventricular Hypertrophy | 2-deoxy-2-[18F]-fluoro-D-glucose positron emission tomography | mechanistic target of rapamycin Activation | Endoplasmic Reticulum Stress | Glucose 6-Phosphate
Journal Article
Journal Article
Metabolism, ISSN 0026-0495, 2015, Volume 64, Issue 2, pp. 296 - 304
Abstract Objective 5′-adenosine monophosphate-activated protein kinase (AMPK) is a key molecule of metabolic enhancement in skeletal muscle. We investigated... 
Endocrinology & Metabolism | Organic cation transporter | 5′-adenosine monophosphate-activated protein kinase | Metformin | Glucose transport | Skeletal muscle | Skeletalmuscle | 5′-adenosine monophosphate-activated | protein kinase | PHOSPHORYLATION | INVOLVEMENT | INCREASES | GLUCOSE-TRANSPORT | ISOFORM | ACETYL-COA CARBOXYLASE | 5 '-adenosine monophosphate-activated protein kinase | DIABETES-MELLITUS | INSULIN | ENDOCRINOLOGY & METABOLISM | AMPK | ALPHA-1-ISOFORM | AMP-Activated Protein Kinases - metabolism | Muscle Fibers, Fast-Twitch - drug effects | Rats, Wistar | Hypoglycemic Agents - metabolism | Muscle Fibers, Fast-Twitch - metabolism | Male | Muscle Fibers, Slow-Twitch - metabolism | Muscle Fibers, Slow-Twitch - drug effects | Metformin - metabolism | Muscle Fibers, Slow-Twitch - enzymology | Organic Cation Transport Proteins - antagonists & inhibitors | Protein Processing, Post-Translational - drug effects | Membrane Transport Modulators - pharmacology | Biological Transport - drug effects | Muscle Fibers, Fast-Twitch - enzymology | Phosphorylation - drug effects | 3-O-Methylglucose - metabolism | Organic Cation Transport Proteins - metabolism | Random Allocation | Enzyme Activation - drug effects | AMP-Activated Protein Kinases - chemistry | Animals | Energy Metabolism | Cimetidine - pharmacology | In Vitro Techniques | Muscles | Adenylic acid | Protein kinases
Journal Article
Nutrition, ISSN 0899-9007, 2015, Volume 32, Issue 5, pp. 553 - 559
Abstract Objective Hydroxycitric acid (HCA), derived from the fruit Garcinia cambogia , reduces the rate of glucose absorption and lowers postprandial glycemia... 
Gastroenterology and Hepatology | 3-O-Methylglucose | Glucose absorption | Glucagon-like peptide-1 | Glucose-dependent insulinotropic polypeptide | Incretin hormones | Postprandial glucose | Hydroxycitric acid | Garcinia cambogia | ACID | GUT | INSULIN SENSITIVITY | GIP | NUTRITION & DIETETICS | HYPERGLYCEMIA | SECRETION | GASTRIC-INHIBITORY POLYPEPTIDE | MOTILITY | Intestinal Mucosa - metabolism | Incretins - blood | Humans | Middle Aged | Diabetes Mellitus, Type 2 - diet therapy | Male | Diabetes Mellitus, Type 2 - metabolism | Dietary Carbohydrates - metabolism | Intestinal Absorption | Glucose - administration & dosage | Citrates - administration & dosage | Hypoglycemic Agents - administration & dosage | Intubation, Gastrointestinal | Duodenum - metabolism | Adult | Female | Dietary Supplements - adverse effects | 3-O-Methylglucose - blood | Biomarkers - metabolism | Dietary Carbohydrates - administration & dosage | Hypoglycemic Agents - therapeutic use | Hyperglycemia - prevention & control | 3-O-Methylglucose - metabolism | Double-Blind Method | Biomarkers - blood | Cross-Over Studies | Citrates - therapeutic use | Diabetes Mellitus, Type 2 - blood | Glucose - metabolism | Incretins - secretion | Aged | Citrates - adverse effects | Hypoglycemic Agents - adverse effects | Type 2 diabetes | Glucose metabolism | Analysis | Information management | Glucose | Dextrose | Diabetes therapy | Plasma | Nutrition research | Hyperglycemia | Polypeptides | Insulin resistance | Diabetes | Insulin | Catheters | Index Medicus
Journal Article