CTRP1 protein enhances fatty acid oxidation via AMP-activated protein kinase (AMPK) activation and acetyl-CoA carboxylase (ACC) inhibition

Journal of Biological Chemistry

Volumn 287, Issue 2, 2012, Pages 1576-1587

  Peterson, Jonathan M ^a   Aja, Susan ^a   Wei, Zhikui ^a   Wong, G William ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYL-COA CARBOXYLASE; AMP-ACTIVATED PROTEIN KINASE; BLOOD GLUCOSE; DOWNSTREAM TARGET; ENERGY EXPENDITURE; EX-VIVO; FAT OXIDATION; FATTY ACID METABOLISM; FATTY ACID OXIDATION; HYPERPHOSPHORYLATED; IN-VIVO; INSULIN SENSITIVITY; METABOLIC STRESS; OBESE MICE; PHYSIOLOGICAL FUNCTIONS; ROSIGLITAZONE; SKELETAL MUSCLE; TRANSGENIC MICE; UPREGULATED EXPRESSION; WEIGHT GAIN;

BIOELECTRIC POTENTIALS; ENZYME ACTIVITY; GLUCOSE; MAMMALS; METABOLISM; MUSCLE; NUTRITION; OXIDATION; PHOSPHORYLATION; PHYSIOLOGY; PROTEINS;

FATTY ACIDS;

ACETYL COENZYME A CARBOXYLASE; ADIPOCYTOKINE; CHOLESTEROL; FATTY ACID; GLUCOSE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE KINASE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE KINASE ALPHA; INSULIN; LEPTIN; PLASMINOGEN ACTIVATOR INHIBITOR 1; PROTEIN CTRP1; RECOMBINANT PROTEIN; RESISTIN; TRIACYLGLYCEROL; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BODY COMPOSITION; BODY WEIGHT; CONTROLLED STUDY; DIET; DRUG ACTIVITY; ENERGY EXPENDITURE; ENZYME ACTIVATION; ENZYME INHIBITION; ENZYME PHOSPHORYLATION; EX VIVO STUDY; FATTY ACID METABOLISM; FATTY ACID OXIDATION; GENE OVEREXPRESSION; IN VIVO STUDY; INSULIN SENSITIVITY; LIPID DIET; MALE; METABOLIC REGULATION; MITOCHONDRIAL RESPIRATION; MOUSE; NONHUMAN; OBESITY; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SKELETAL MUSCLE; SOLEUS MUSCLE; WEIGHT GAIN;

ACETYL-COA CARBOXYLASE; ADIPOKINES; ADIPOSITY; AMP-ACTIVATED PROTEIN KINASES; ANIMALS; DIETARY FATS; ENERGY METABOLISM; FATTY ACIDS; MALE; MICE; MICE, TRANSGENIC; MUSCLE PROTEINS; MUSCLE, SKELETAL; OXIDATION-REDUCTION; SIGNAL TRANSDUCTION;

MUS; MUS MUSCULUS;

EID: 84855511415     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M111.278333     Document Type: Article

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