Endocrinology, ISSN 0013-7227, 10/2013, Volume 154, Issue 10, pp. 3539 - 3551
Increased hepatic glucose production is a key pathophysiological feature of type 2 diabetes. Like all other cell types, hepatocytes express many G...
Diabetes-Insulin-Glucagon-Gastrointestinal
Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 07/2012, Volume 153, Issue 7, pp. 3054 - 3065
The intestine secretes a range of hormones with important local and distant actions, including the control of insulin secretion and appetite. A number of...
GLP-1 | GLUCAGON-LIKE PEPTIDE-1 | GLUCOSE | GASTROINTESTINAL-TRACT | ENTEROENDOCRINE CELLS | LINE | ENDOCRINOLOGY & METABOLISM | PANCREATIC BETA-CELLS | DEPENDENT INSULINOTROPIC POLYPEPTIDE | DIFFERENTIATION | GIP | Flow Cytometry - methods | Oligonucleotide Array Sequence Analysis | Peptides - chemistry | Cell Separation | Mice, Inbred C57BL | Gene Expression Profiling | Intestines - metabolism | Enteroendocrine Cells - cytology | Transcription Factors - metabolism | Cholecystokinin - metabolism | Animals | Models, Biological | Transcription, Genetic | Chromogranin A - metabolism | Mice | Intestine, Small - metabolism | Intestines - cytology | Diabetes-Insulin-Glucagon-Gastrointestinal
GLP-1 | GLUCAGON-LIKE PEPTIDE-1 | GLUCOSE | GASTROINTESTINAL-TRACT | ENTEROENDOCRINE CELLS | LINE | ENDOCRINOLOGY & METABOLISM | PANCREATIC BETA-CELLS | DEPENDENT INSULINOTROPIC POLYPEPTIDE | DIFFERENTIATION | GIP | Flow Cytometry - methods | Oligonucleotide Array Sequence Analysis | Peptides - chemistry | Cell Separation | Mice, Inbred C57BL | Gene Expression Profiling | Intestines - metabolism | Enteroendocrine Cells - cytology | Transcription Factors - metabolism | Cholecystokinin - metabolism | Animals | Models, Biological | Transcription, Genetic | Chromogranin A - metabolism | Mice | Intestine, Small - metabolism | Intestines - cytology | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 08/2012, Volume 153, Issue 8, pp. 3613 - 3619
Gastric bypass leads to the remission of type 2 diabetes independently of weight loss. Our hypothesis is that changes in bile flow due to the altered anatomy...
PEPTIDE-YY | GUT HORMONES | ENERGY-EXPENDITURE | OBESE SUBJECTS | THERAPY | GLUCOSE-METABOLISM | ACIDS | ENDOCRINOLOGY & METABOLISM | FARNESOID-X-RECEPTOR | BARIATRIC SURGERY | TYPE-2 DIABETES-MELLITUS | Gastric Bypass | Bile Acids and Salts - blood | C-Reactive Protein | Rats, Wistar | Humans | Middle Aged | Bile - physiology | Rats | Glucagon-Like Peptide 1 - blood | Male | Animals | Fibroblast Growth Factors - blood | Dogs | Weight Loss - physiology | Adult | Calorimetry | Female | Peptide YY - blood | Diabetes Mellitus, Type 2 | Blood Glucose - metabolism | Diabetes-Insulin-Glucagon-Gastrointestinal
PEPTIDE-YY | GUT HORMONES | ENERGY-EXPENDITURE | OBESE SUBJECTS | THERAPY | GLUCOSE-METABOLISM | ACIDS | ENDOCRINOLOGY & METABOLISM | FARNESOID-X-RECEPTOR | BARIATRIC SURGERY | TYPE-2 DIABETES-MELLITUS | Gastric Bypass | Bile Acids and Salts - blood | C-Reactive Protein | Rats, Wistar | Humans | Middle Aged | Bile - physiology | Rats | Glucagon-Like Peptide 1 - blood | Male | Animals | Fibroblast Growth Factors - blood | Dogs | Weight Loss - physiology | Adult | Calorimetry | Female | Peptide YY - blood | Diabetes Mellitus, Type 2 | Blood Glucose - metabolism | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 11/2015, Volume 156, Issue 11, pp. 3961 - 3970
Bile acids are well-recognized stimuli of glucagon-like peptide-1 (GLP-1) secretion. This action has been attributed to activation of the G protein–coupled...
RESPONSES | CELLS | TGR5 | GASTRIC BYPASS-SURGERY | ACTIVATION | GLUCAGON-LIKE PEPTIDE-1 | GLUCOSE-METABOLISM | TOLERANCE | MOUSE | ENDOCRINOLOGY & METABOLISM | SECRETION | Bile Acids and Salts - pharmacology | Intracellular Space - drug effects | Glucagon-Like Peptide 1 - metabolism | Rats, Wistar | Receptors, G-Protein-Coupled - metabolism | Calcium - metabolism | Tissue Culture Techniques | Cells, Cultured | Male | Mice, Transgenic | Glucagon-Like Peptide 1 - secretion | Mice, Knockout | Animals | Intestine, Small - drug effects | Intracellular Space - metabolism | Receptors, G-Protein-Coupled - genetics | Enteroendocrine Cells - metabolism | Intestine, Small - metabolism | Enteroendocrine Cells - drug effects | Taurodeoxycholic Acid - pharmacology | Cyclic AMP - metabolism | Taurolithocholic Acid - pharmacology | Microscopy, Fluorescence | Original Research
RESPONSES | CELLS | TGR5 | GASTRIC BYPASS-SURGERY | ACTIVATION | GLUCAGON-LIKE PEPTIDE-1 | GLUCOSE-METABOLISM | TOLERANCE | MOUSE | ENDOCRINOLOGY & METABOLISM | SECRETION | Bile Acids and Salts - pharmacology | Intracellular Space - drug effects | Glucagon-Like Peptide 1 - metabolism | Rats, Wistar | Receptors, G-Protein-Coupled - metabolism | Calcium - metabolism | Tissue Culture Techniques | Cells, Cultured | Male | Mice, Transgenic | Glucagon-Like Peptide 1 - secretion | Mice, Knockout | Animals | Intestine, Small - drug effects | Intracellular Space - metabolism | Receptors, G-Protein-Coupled - genetics | Enteroendocrine Cells - metabolism | Intestine, Small - metabolism | Enteroendocrine Cells - drug effects | Taurodeoxycholic Acid - pharmacology | Cyclic AMP - metabolism | Taurolithocholic Acid - pharmacology | Microscopy, Fluorescence | Original Research
Journal Article
Endocrinology, ISSN 0013-7227, 10/2011, Volume 152, Issue 10, pp. 3622 - 3627
Enhanced levels of nuclear factor (NF)-κB-inducing kinase (NIK), an upstream kinase in the NF-κB pathway, have been implicated in the pathogenesis of chronic...
ACTIVATION | OBESITY | PROTEIN | INHIBITOR | ENDOCRINOLOGY & METABOLISM | Diabetes-Insulin-Glucagon-Gastrointestinal
ACTIVATION | OBESITY | PROTEIN | INHIBITOR | ENDOCRINOLOGY & METABOLISM | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
6.
Full Text
Integrated Regulation of Hepatic Metabolism by Fibroblast Growth Factor 21 (FGF21) in Vivo
Endocrinology, ISSN 0013-7227, 08/2011, Volume 152, Issue 8, pp. 2996 - 3004
Fibroblast growth factor (FGF21) plays an important role in regulating hepatic oxidation of fatty acids and gluconeogenesis in response to fasting and during...
BETA-KLOTHO | PPAR-ALPHA | LIPID-METABOLISM | FIBROBLAST-GROWTH-FACTOR-21 | THYROID-HORMONE | PGC-1-ALPHA | ENDOCRINOLOGY & METABOLISM | STATE | ENERGY-METABOLISM | INSULIN SENSITIVITY | EXPRESSION | Humans | Liver - metabolism | Mice, Inbred C57BL | Male | Forkhead Transcription Factors - physiology | Extracellular Signal-Regulated MAP Kinases - metabolism | Organ Specificity | MAP Kinase Signaling System | Trans-Activators - physiology | Animals | Membrane Proteins - physiology | PPAR alpha - physiology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Trans-Activators - genetics | Forkhead Box Protein O1 | Mice | Transcription Factors | Fibroblast Growth Factors - physiology | Gluconeogenesis | Diabetes-Insulin-Glucagon-Gastrointestinal
BETA-KLOTHO | PPAR-ALPHA | LIPID-METABOLISM | FIBROBLAST-GROWTH-FACTOR-21 | THYROID-HORMONE | PGC-1-ALPHA | ENDOCRINOLOGY & METABOLISM | STATE | ENERGY-METABOLISM | INSULIN SENSITIVITY | EXPRESSION | Humans | Liver - metabolism | Mice, Inbred C57BL | Male | Forkhead Transcription Factors - physiology | Extracellular Signal-Regulated MAP Kinases - metabolism | Organ Specificity | MAP Kinase Signaling System | Trans-Activators - physiology | Animals | Membrane Proteins - physiology | PPAR alpha - physiology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Trans-Activators - genetics | Forkhead Box Protein O1 | Mice | Transcription Factors | Fibroblast Growth Factors - physiology | Gluconeogenesis | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 02/2011, Volume 152, Issue 2, pp. 405 - 413
The effects of chemical (DPP-4) inhibition and genetic reduction of DPP-4 activity on bone quality were studied in wild-type and ovariectomized mice....
SYSTEM | INSULIN | TRANSPORT | CELL-LINE | ENDOCRINOLOGY & METABOLISM | Glucagon-Like Peptide 1 - metabolism | Oligonucleotide Array Sequence Analysis | Calcium - metabolism | Cells, Cultured | Signal Transduction - genetics | Glucagon-Like Peptide 1 - secretion | Animals | Flow Cytometry | Signal Transduction - drug effects | Fluorescence Resonance Energy Transfer | Mice | Glutamine - pharmacology | Cyclic AMP - metabolism | Diabetes-Insulin-Glucagon-Gastrointestinal
SYSTEM | INSULIN | TRANSPORT | CELL-LINE | ENDOCRINOLOGY & METABOLISM | Glucagon-Like Peptide 1 - metabolism | Oligonucleotide Array Sequence Analysis | Calcium - metabolism | Cells, Cultured | Signal Transduction - genetics | Glucagon-Like Peptide 1 - secretion | Animals | Flow Cytometry | Signal Transduction - drug effects | Fluorescence Resonance Energy Transfer | Mice | Glutamine - pharmacology | Cyclic AMP - metabolism | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 02/2015, Volume 156, Issue 2, pp. 444 - 452
The physiological role of serotonin, or 5-hydroxytryptamine (5-HT), in pancreatic β-cell function was previously elucidated using a pregnant mouse model....
BETA-CELL GROWTH | ISLETS | MOUSE | MASS | ENDOCRINOLOGY & METABOLISM | DETERMINANT | RATS | RECEPTOR | MECHANISMS | SUBSET | Insulin-Secreting Cells - physiology | Serotonin - physiology | Insulin Resistance | Male | Receptors, Serotonin - genetics | Receptors, Serotonin - metabolism | Mice, Knockout | Tryptophan Hydroxylase - genetics | Insulin - metabolism | Animals | Diet, High-Fat | Insulin Secretion | Tryptophan Hydroxylase - metabolism | Diabetes-Insulin-Glucagon-Gastrointestinal
BETA-CELL GROWTH | ISLETS | MOUSE | MASS | ENDOCRINOLOGY & METABOLISM | DETERMINANT | RATS | RECEPTOR | MECHANISMS | SUBSET | Insulin-Secreting Cells - physiology | Serotonin - physiology | Insulin Resistance | Male | Receptors, Serotonin - genetics | Receptors, Serotonin - metabolism | Mice, Knockout | Tryptophan Hydroxylase - genetics | Insulin - metabolism | Animals | Diet, High-Fat | Insulin Secretion | Tryptophan Hydroxylase - metabolism | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 09/2013, Volume 154, Issue 9, pp. 3099 - 3109
Fibroblast growth factor 21 (FGF21) is a potent regulator of glucose and lipid metabolism and is currently being pursued as a therapeutic agent for insulin...
INDUCED HEPATIC STEATOSIS | GLUCOSE-HOMEOSTASIS | INCREASED EXPRESSION | METABOLISM | FATTY LIVER-DISEASE | INCREASES ENERGY-EXPENDITURE | MITOCHONDRIAL-FUNCTION | ENDOCRINOLOGY & METABOLISM | RESISTANCE | MUSCLE | GROWTH-FACTOR 21 | Glucose Intolerance - metabolism | Recombinant Proteins - therapeutic use | Adipose Tissue, Brown - surgery | Liver - pathology | Humans | Protein Kinase C-theta | Diet, High-Fat - adverse effects | Drug Implants | Male | Muscle, Skeletal - metabolism | Glucose Intolerance - pathology | Fibroblast Growth Factors - metabolism | Glucose Intolerance - drug therapy | Lipectomy | Liver - drug effects | Fibroblast Growth Factors - administration & dosage | Glucose Intolerance - etiology | Isoenzymes - metabolism | Protein Kinase C - metabolism | Muscle, Skeletal - drug effects | Fibroblast Growth Factors - therapeutic use | Recombinant Proteins - metabolism | Liver - metabolism | Mice, Inbred C57BL | Cells, Cultured | Insulin Resistance | Recombinant Proteins - administration & dosage | Infusions, Subcutaneous | Animals | Protein Kinase C-epsilon - metabolism | Lipid Metabolism - drug effects | Adipose Tissue, Brown - drug effects | Adipose Tissue, Brown - metabolism | Mice | Muscle, Skeletal - pathology | Energy Metabolism - drug effects | Diabetes-Insulin-Glucagon-Gastrointestinal
INDUCED HEPATIC STEATOSIS | GLUCOSE-HOMEOSTASIS | INCREASED EXPRESSION | METABOLISM | FATTY LIVER-DISEASE | INCREASES ENERGY-EXPENDITURE | MITOCHONDRIAL-FUNCTION | ENDOCRINOLOGY & METABOLISM | RESISTANCE | MUSCLE | GROWTH-FACTOR 21 | Glucose Intolerance - metabolism | Recombinant Proteins - therapeutic use | Adipose Tissue, Brown - surgery | Liver - pathology | Humans | Protein Kinase C-theta | Diet, High-Fat - adverse effects | Drug Implants | Male | Muscle, Skeletal - metabolism | Glucose Intolerance - pathology | Fibroblast Growth Factors - metabolism | Glucose Intolerance - drug therapy | Lipectomy | Liver - drug effects | Fibroblast Growth Factors - administration & dosage | Glucose Intolerance - etiology | Isoenzymes - metabolism | Protein Kinase C - metabolism | Muscle, Skeletal - drug effects | Fibroblast Growth Factors - therapeutic use | Recombinant Proteins - metabolism | Liver - metabolism | Mice, Inbred C57BL | Cells, Cultured | Insulin Resistance | Recombinant Proteins - administration & dosage | Infusions, Subcutaneous | Animals | Protein Kinase C-epsilon - metabolism | Lipid Metabolism - drug effects | Adipose Tissue, Brown - drug effects | Adipose Tissue, Brown - metabolism | Mice | Muscle, Skeletal - pathology | Energy Metabolism - drug effects | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 03/2013, Volume 154, Issue 3, pp. 1021 - 1028
Estrogen replacement therapy reduces the incidence of type 2 diabetes in postmenopausal women; however, the mechanism is unknown. Therefore, the aim of this...
ACTIVATION | HEALTH | PROGESTERONE | ESTROGEN SULFOTRANSFERASE | SEX | ENDOCRINOLOGY & METABOLISM | Estrogen Replacement Therapy | Humans | Diet, High-Fat - adverse effects | Muscle, Skeletal - metabolism | Diabetes Mellitus, Type 2 - metabolism | Liver - drug effects | Insulin Resistance - physiology | Protein Kinase C - metabolism | Muscle, Skeletal - drug effects | Female | Models, Animal | Homeostasis - drug effects | Estradiol - pharmacology | Estradiol - metabolism | Ovariectomy | Liver - metabolism | Diabetes Mellitus, Type 2 - prevention & control | Estradiol - deficiency | Eating - drug effects | Animals | Menopause - metabolism | Lipid Metabolism - drug effects | Glucose - metabolism | Mice | Energy Metabolism - drug effects | Diabetes-Insulin-Glucagon-Gastrointestinal
ACTIVATION | HEALTH | PROGESTERONE | ESTROGEN SULFOTRANSFERASE | SEX | ENDOCRINOLOGY & METABOLISM | Estrogen Replacement Therapy | Humans | Diet, High-Fat - adverse effects | Muscle, Skeletal - metabolism | Diabetes Mellitus, Type 2 - metabolism | Liver - drug effects | Insulin Resistance - physiology | Protein Kinase C - metabolism | Muscle, Skeletal - drug effects | Female | Models, Animal | Homeostasis - drug effects | Estradiol - pharmacology | Estradiol - metabolism | Ovariectomy | Liver - metabolism | Diabetes Mellitus, Type 2 - prevention & control | Estradiol - deficiency | Eating - drug effects | Animals | Menopause - metabolism | Lipid Metabolism - drug effects | Glucose - metabolism | Mice | Energy Metabolism - drug effects | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 03/2014, Volume 155, Issue 3, pp. 758 - 768
It has been established that intracellular calcium homeostasis is critical for survival and function of pancreatic β-cells. However, the role of endoplasmic...
DIABETES-MELLITUS | APOPTOSIS | WFS1 GENE | ACTIVATION | UBIQUITOUS CALPAINS PROMOTE | INS GENE | ER STRESS | WOLFRAM-SYNDROME | ENDOCRINOLOGY & METABOLISM | THIOREDOXIN-INTERACTING PROTEIN | FATTY-ACIDS | Sarcoplasmic Reticulum Calcium-Transporting ATPases - metabolism | Calcium - metabolism | Cell Separation | Humans | Cells, Cultured | Endoplasmic Reticulum - metabolism | Homeostasis | Male | Plasmids - metabolism | Animals | Flow Cytometry | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Cell Death | HEK293 Cells | Fluorescence Resonance Energy Transfer | Mice | Insulin-Secreting Cells - pathology | Fatty Acids - metabolism | Real-Time Polymerase Chain Reaction | Diabetes-Insulin-Glucagon-Gastrointestinal
DIABETES-MELLITUS | APOPTOSIS | WFS1 GENE | ACTIVATION | UBIQUITOUS CALPAINS PROMOTE | INS GENE | ER STRESS | WOLFRAM-SYNDROME | ENDOCRINOLOGY & METABOLISM | THIOREDOXIN-INTERACTING PROTEIN | FATTY-ACIDS | Sarcoplasmic Reticulum Calcium-Transporting ATPases - metabolism | Calcium - metabolism | Cell Separation | Humans | Cells, Cultured | Endoplasmic Reticulum - metabolism | Homeostasis | Male | Plasmids - metabolism | Animals | Flow Cytometry | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Cell Death | HEK293 Cells | Fluorescence Resonance Energy Transfer | Mice | Insulin-Secreting Cells - pathology | Fatty Acids - metabolism | Real-Time Polymerase Chain Reaction | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 02/2011, Volume 152, Issue 2, pp. 394 - 404
Leptin action in the brain normalizes diabetic hyperglycemia by suppressing hepatic glucose production while increasing tissue glucose uptake despite severe...
PROTEIN-2 MESSENGER-RNA | HYPERPHAGIA | FOOD-INTAKE | PROOPIOMELANOCORTIN NEURONS | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | RATS | RESISTANCE | SENSITIVITY | PERIPHERAL-TISSUES | GLUCOSE-PRODUCTION | Insulin - pharmacology | Diabetes Mellitus, Experimental - drug therapy | Glucose Tolerance Test | Rats, Wistar | Rats | Male | Reverse Transcriptase Polymerase Chain Reaction | Glucagon - blood | Hyperglycemia - drug therapy | Blood Glucose - drug effects | Brain - drug effects | Brain - metabolism | Diabetes Mellitus, Experimental - blood | Animals | Hyperglycemia - blood | Body Composition - drug effects | Leptin - pharmacology | Corticosterone - blood | Diabetes-Insulin-Glucagon-Gastrointestinal
PROTEIN-2 MESSENGER-RNA | HYPERPHAGIA | FOOD-INTAKE | PROOPIOMELANOCORTIN NEURONS | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | RATS | RESISTANCE | SENSITIVITY | PERIPHERAL-TISSUES | GLUCOSE-PRODUCTION | Insulin - pharmacology | Diabetes Mellitus, Experimental - drug therapy | Glucose Tolerance Test | Rats, Wistar | Rats | Male | Reverse Transcriptase Polymerase Chain Reaction | Glucagon - blood | Hyperglycemia - drug therapy | Blood Glucose - drug effects | Brain - drug effects | Brain - metabolism | Diabetes Mellitus, Experimental - blood | Animals | Hyperglycemia - blood | Body Composition - drug effects | Leptin - pharmacology | Corticosterone - blood | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 02/2012, Volume 153, Issue 2, pp. 631 - 646
Dysregulation of blood glucose and triglycerides are the major characteristics of type 2 diabetes mellitus. We sought to identify the mechanisms regulating...
REGULATES LIPID-METABOLISM | FORKHEAD TRANSCRIPTION FACTOR | PHOSPHOENOLPYRUVATE CARBOXYKINASE | INSULIN-RESPONSE SEQUENCE | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | FACTOR-BINDING PROTEIN-1 | KINASE-B | NUTRIENT HOMEOSTASIS | SIGNALING CASCADE | GLUCOSE-PRODUCTION | Hyperlipidemias - metabolism | Liver - metabolism | Gene Expression Regulation | Homeostasis | Forkhead Transcription Factors - genetics | Hypoglycemia - metabolism | Mice, Knockout | Gluconeogenesis - physiology | Animals | Forkhead Transcription Factors - metabolism | Glucose - metabolism | Mice, Inbred NOD | Forkhead Box Protein O1 | Mice | Blood Glucose - metabolism | Forkhead Box Protein O3 | Lipid Metabolism - physiology | Diabetes-Insulin-Glucagon-Gastrointestinal
REGULATES LIPID-METABOLISM | FORKHEAD TRANSCRIPTION FACTOR | PHOSPHOENOLPYRUVATE CARBOXYKINASE | INSULIN-RESPONSE SEQUENCE | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | FACTOR-BINDING PROTEIN-1 | KINASE-B | NUTRIENT HOMEOSTASIS | SIGNALING CASCADE | GLUCOSE-PRODUCTION | Hyperlipidemias - metabolism | Liver - metabolism | Gene Expression Regulation | Homeostasis | Forkhead Transcription Factors - genetics | Hypoglycemia - metabolism | Mice, Knockout | Gluconeogenesis - physiology | Animals | Forkhead Transcription Factors - metabolism | Glucose - metabolism | Mice, Inbred NOD | Forkhead Box Protein O1 | Mice | Blood Glucose - metabolism | Forkhead Box Protein O3 | Lipid Metabolism - physiology | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 10/2011, Volume 152, Issue 10, pp. 3648 - 3660
Although thiazolidinediones (TZD) effectively improve hyperglycemia and increase adiponectin, a proinsulin-sensitizing adipokine, they also increase...
3T3-L1 ADIPOCYTES | LIPID-ACCUMULATION | IN-VITRO | HUMAN ADENOVIRUS TYPE-36 | ENDOCRINOLOGY & METABOLISM | ACTIVATED-RECEPTOR-GAMMA | MICE | DIFFERENTIATION | INSULIN SENSITIVITY | AGONISTS | ADIPOSE-TISSUE | Diabetes-Insulin-Glucagon-Gastrointestinal
3T3-L1 ADIPOCYTES | LIPID-ACCUMULATION | IN-VITRO | HUMAN ADENOVIRUS TYPE-36 | ENDOCRINOLOGY & METABOLISM | ACTIVATED-RECEPTOR-GAMMA | MICE | DIFFERENTIATION | INSULIN SENSITIVITY | AGONISTS | ADIPOSE-TISSUE | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 03/2014, Volume 155, Issue 3, pp. 769 - 782
Lipid metabolism is tightly regulated by nuclear receptors, transcription factors, and cellular enzymes. In this study, we demonstrated that the liver-enriched...
PPAR-ALPHA | OBESITY | FIBROBLAST-GROWTH-FACTOR-21 | DISEASE | ENDOCRINOLOGY & METABOLISM | ELEMENT-BINDING PROTEIN | MICE | STEATOHEPATITIS | STRESS | IDENTIFICATION | GROWTH-FACTOR 21 | Promoter Regions, Genetic | Liver - metabolism | Gene Expression Regulation | Homeostasis | Molecular Sequence Data | Recombinant Proteins - chemistry | Male | Hepatocytes - metabolism | Sequence Homology, Nucleic Acid | Amino Acid Motifs | Mice, Knockout | Triglycerides - metabolism | Cyclic AMP Response Element-Binding Protein - genetics | Fibroblast Growth Factors - metabolism | Lipids - chemistry | Animals | Base Sequence | Cyclic AMP Response Element-Binding Protein - metabolism | Protein Binding | Mice | PPAR alpha - metabolism | Fatty Acids - metabolism | Diabetes-Insulin-Glucagon-Gastrointestinal
PPAR-ALPHA | OBESITY | FIBROBLAST-GROWTH-FACTOR-21 | DISEASE | ENDOCRINOLOGY & METABOLISM | ELEMENT-BINDING PROTEIN | MICE | STEATOHEPATITIS | STRESS | IDENTIFICATION | GROWTH-FACTOR 21 | Promoter Regions, Genetic | Liver - metabolism | Gene Expression Regulation | Homeostasis | Molecular Sequence Data | Recombinant Proteins - chemistry | Male | Hepatocytes - metabolism | Sequence Homology, Nucleic Acid | Amino Acid Motifs | Mice, Knockout | Triglycerides - metabolism | Cyclic AMP Response Element-Binding Protein - genetics | Fibroblast Growth Factors - metabolism | Lipids - chemistry | Animals | Base Sequence | Cyclic AMP Response Element-Binding Protein - metabolism | Protein Binding | Mice | PPAR alpha - metabolism | Fatty Acids - metabolism | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 02/2015, Volume 156, Issue 2, pp. 437 - 443
Chronic intermittent hypoxia during sleep (IH), as occurs in sleep apnea, promotes systemic insulin resistance. Resveratrol (Resv) has been reported to...
OBSTRUCTIVE SLEEP-APNEA | MURINE MODEL | SPATIAL-LEARNING DEFICITS | INFLAMMATION | MITOCHONDRIAL-FUNCTION | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | NITRIC-OXIDE | POSITIVE AIRWAY PRESSURE | DIET-INDUCED OBESITY | HUMAN ADIPOCYTES | Intra-Abdominal Fat - immunology | Eating | Mice, Inbred C57BL | Insulin Resistance | Male | Hypoxia - immunology | Random Allocation | Stilbenes - pharmacology | Insulin - blood | Animals | Leptin - blood | Macrophages - drug effects | Drug Evaluation, Preclinical | Weight Gain | Anti-Obesity Agents - pharmacology | Diabetes-Insulin-Glucagon-Gastrointestinal
OBSTRUCTIVE SLEEP-APNEA | MURINE MODEL | SPATIAL-LEARNING DEFICITS | INFLAMMATION | MITOCHONDRIAL-FUNCTION | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | NITRIC-OXIDE | POSITIVE AIRWAY PRESSURE | DIET-INDUCED OBESITY | HUMAN ADIPOCYTES | Intra-Abdominal Fat - immunology | Eating | Mice, Inbred C57BL | Insulin Resistance | Male | Hypoxia - immunology | Random Allocation | Stilbenes - pharmacology | Insulin - blood | Animals | Leptin - blood | Macrophages - drug effects | Drug Evaluation, Preclinical | Weight Gain | Anti-Obesity Agents - pharmacology | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 09/2014, Volume 155, Issue 9, pp. 3302 - 3314
Nutrient intake regulates intestinal epithelial mass and crypt proliferation. Recent findings in model organisms and rodents indicate nutrient restriction...
HIGH-FAT DIET | GLUCAGON-LIKE PEPTIDE-2 | ENTEROENDOCRINE CELLS | DISTINCT | ENDOCRINOLOGY & METABOLISM | RATS | MICE | PROLIFERATION | BETA-CATENIN | ENTERAL NUTRIENTS | GROWTH-FACTOR-I | Cell Proliferation | Signal Transduction | Humans | Diet, High-Fat - adverse effects | Male | Mice, Transgenic | Obesity - physiopathology | Intestines - metabolism | Stem Cells - cytology | Stem Cells - metabolism | Obesity - genetics | Obesity - metabolism | Insulin - metabolism | Animals | Female | Mice | Insulin-Like Growth Factor I - metabolism | Intestines - cytology | Diabetes-Insulin-Glucagon-Gastrointestinal
HIGH-FAT DIET | GLUCAGON-LIKE PEPTIDE-2 | ENTEROENDOCRINE CELLS | DISTINCT | ENDOCRINOLOGY & METABOLISM | RATS | MICE | PROLIFERATION | BETA-CATENIN | ENTERAL NUTRIENTS | GROWTH-FACTOR-I | Cell Proliferation | Signal Transduction | Humans | Diet, High-Fat - adverse effects | Male | Mice, Transgenic | Obesity - physiopathology | Intestines - metabolism | Stem Cells - cytology | Stem Cells - metabolism | Obesity - genetics | Obesity - metabolism | Insulin - metabolism | Animals | Female | Mice | Insulin-Like Growth Factor I - metabolism | Intestines - cytology | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 08/2011, Volume 152, Issue 8, pp. 3030 - 3039
Sexual dimorphism and supplementation studies suggest an important role for estrogens in the amelioration of glucose intolerance and diabetes. Because little...
BREAST-CANCER | GROWTH-FACTOR RECEPTOR | PLASMA-MEMBRANE RECEPTOR | HUMAN ISLETS | PHOSPHATIDYLINOSITOL 3-KINASE | IN-VIVO | FEMALE MICE | ENDOCRINOLOGY & METABOLISM | G-PROTEIN-COUPLED-RECEPTOR-30 GPR30 | 17-BETA-ESTRADIOL | ER-ALPHA | Amino Acid Sequence | Receptors, Estrogen | Calcium - metabolism | Mice, Inbred C57BL | Cercopithecus aethiops | Molecular Sequence Data | Phosphatidylinositol 3-Kinases - metabolism | Cyclopentanes - pharmacology | Extracellular Signal-Regulated MAP Kinases - metabolism | Quinolines - pharmacology | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Animals | Insulin-Secreting Cells - drug effects | Cell Line, Tumor | Female | Mice | COS Cells | Insulin Secretion | Estradiol - pharmacology | Receptors, G-Protein-Coupled - physiology | Diabetes-Insulin-Glucagon-Gastrointestinal
BREAST-CANCER | GROWTH-FACTOR RECEPTOR | PLASMA-MEMBRANE RECEPTOR | HUMAN ISLETS | PHOSPHATIDYLINOSITOL 3-KINASE | IN-VIVO | FEMALE MICE | ENDOCRINOLOGY & METABOLISM | G-PROTEIN-COUPLED-RECEPTOR-30 GPR30 | 17-BETA-ESTRADIOL | ER-ALPHA | Amino Acid Sequence | Receptors, Estrogen | Calcium - metabolism | Mice, Inbred C57BL | Cercopithecus aethiops | Molecular Sequence Data | Phosphatidylinositol 3-Kinases - metabolism | Cyclopentanes - pharmacology | Extracellular Signal-Regulated MAP Kinases - metabolism | Quinolines - pharmacology | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Animals | Insulin-Secreting Cells - drug effects | Cell Line, Tumor | Female | Mice | COS Cells | Insulin Secretion | Estradiol - pharmacology | Receptors, G-Protein-Coupled - physiology | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article
Endocrinology, ISSN 0013-7227, 10/2011, Volume 152, Issue 10, pp. 3638 - 3647
Insulin resistance (IR) is the major feature of metabolic syndrome, including type 2 diabetes. IR studies are mainly focused on peripheral tissues, such as...
OXIDATIVE STRESS | SIGNALING PATHWAYS | METABOLIC SYNDROME | PHOSPHATIDYLINOSITOL 3-KINASE | PROTEIN EXPRESSION | ENDOCRINOLOGY & METABOLISM | MITOCHONDRIAL DYSFUNCTION | GROWTH-FACTOR | DIABETIC-NEUROPATHY | HUMAN SKELETAL-MUSCLE | RECEPTOR SUBSTRATE-1 | Hyperinsulinism - metabolism | Phosphorylation | Animals | Mice, Inbred C57BL | Insulin Resistance | Rats | Mice | Extracellular Signal-Regulated MAP Kinases - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Rats, Sprague-Dawley | Ganglia, Spinal - metabolism | 500 | Diabetes-Insulin-Glucagon-Gastrointestinal | 300
OXIDATIVE STRESS | SIGNALING PATHWAYS | METABOLIC SYNDROME | PHOSPHATIDYLINOSITOL 3-KINASE | PROTEIN EXPRESSION | ENDOCRINOLOGY & METABOLISM | MITOCHONDRIAL DYSFUNCTION | GROWTH-FACTOR | DIABETIC-NEUROPATHY | HUMAN SKELETAL-MUSCLE | RECEPTOR SUBSTRATE-1 | Hyperinsulinism - metabolism | Phosphorylation | Animals | Mice, Inbred C57BL | Insulin Resistance | Rats | Mice | Extracellular Signal-Regulated MAP Kinases - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Rats, Sprague-Dawley | Ganglia, Spinal - metabolism | 500 | Diabetes-Insulin-Glucagon-Gastrointestinal | 300
Journal Article
Endocrinology, ISSN 0013-7227, 08/2011, Volume 152, Issue 8, pp. 3074 - 3081
Obesity is frequently associated with an infiltration of macrophages into adipose tissue. Adipocyte dysfunction causes a phenotypic switch of macrophages from...
CELLS | INFLAMMATION | ENDOCRINOLOGY & METABOLISM | FAT | MICE | DEATH | DYSFUNCTION | DIET-INDUCED OBESITY | POLARIZATION | EXPRESSION | INDUCED INSULIN-RESISTANCE | Macrophages - physiology | Antigens, Differentiation - analysis | Cell Polarity | Adipose Tissue - physiology | Receptors, Cell Surface - analysis | Asialoglycoproteins - analysis | Male | CD11c Antigen - analysis | Adipocytes - physiology | Inflammation - etiology | Membrane Proteins - analysis | Macrophage Activation | Animals | CD11c Antigen - genetics | Lectins, C-Type - analysis | Mannose-Binding Lectins - analysis | Antigens, Differentiation - genetics | Mice | Apoptosis | Diabetes-Insulin-Glucagon-Gastrointestinal
CELLS | INFLAMMATION | ENDOCRINOLOGY & METABOLISM | FAT | MICE | DEATH | DYSFUNCTION | DIET-INDUCED OBESITY | POLARIZATION | EXPRESSION | INDUCED INSULIN-RESISTANCE | Macrophages - physiology | Antigens, Differentiation - analysis | Cell Polarity | Adipose Tissue - physiology | Receptors, Cell Surface - analysis | Asialoglycoproteins - analysis | Male | CD11c Antigen - analysis | Adipocytes - physiology | Inflammation - etiology | Membrane Proteins - analysis | Macrophage Activation | Animals | CD11c Antigen - genetics | Lectins, C-Type - analysis | Mannose-Binding Lectins - analysis | Antigens, Differentiation - genetics | Mice | Apoptosis | Diabetes-Insulin-Glucagon-Gastrointestinal
Journal Article