Loss of circadian rhythm of circulating insulin concentration induced by high-fat diet intake is associated with disrupted rhythmic expression of circadian clock genes in the liver

Metabolism: Clinical and Experimental

Volumn 65, Issue 4, 2016, Pages 482-491

  Honma, Kazue ^a   Hikosaka, Maki ^a   Mochizuki, Kazuki ^a,b   Goda, Toshinao ^a  

^a UNIVERSITY OF SHIZUOKA   (Japan)

^b UNIVERSITY OF YAMANASHI   (Japan)

Author keywords

Circadian rhythm; Clock gene; High fat diet; Lipid metabolism; Liver

Indexed keywords

ACETYL COA CARBOXYLASE BETA; ACETYL COENZYME A CARBOXYLASE; CARBOHYDRATE RESPONSIVE ELEMENT BINDING PROTEIN; CRYPTOCHROME 1; CRYPTOCHROME 2; FATTY ACID SYNTHASE; GLUCOSE; INSULIN; MESSENGER RNA; NUCLEAR FACTOR INTERLEUKIN 3 REGULATOR PROTEIN; NUCLEAR RECEPTOR NR1D1; NUCLEAR RECEPTOR SUBFAMILY 1 GROUP D MEMBER 2; PEPTIDES AND PROTEINS; PER1 PROTEIN; PER2 PROTEIN; PER3 PROTEIN; PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR ARNTL; TRANSCRIPTION FACTOR CLOCK; UNCLASSIFIED DRUG; CIRCADIAN RHYTHM SIGNALING PROTEIN; GLUCOSE BLOOD LEVEL;

ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CIRCADIAN RHYTHM; CONTROLLED STUDY; FEEDBACK SYSTEM; GENE DISRUPTION; GENE EXPRESSION REGULATION; GENETIC ASSOCIATION; GLUCOSE BLOOD LEVEL; HYPERINSULINEMIA; INSULIN BLOOD LEVEL; INSULIN RELEASE; INSULIN RESISTANCE; LIGHT DARK CYCLE; LIPID DIET; LIPOGENESIS; LIVER; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; ANIMAL; BIOSYNTHESIS; BLOOD; BODY WEIGHT; DRUG EFFECTS; GENE EXPRESSION; GENETICS; INSTITUTE FOR CANCER RESEARCH MOUSE; METABOLISM; ORGAN SIZE;

ANIMALS; BLOOD GLUCOSE; BODY WEIGHT; CIRCADIAN CLOCKS; CIRCADIAN RHYTHM SIGNALING PEPTIDES AND PROTEINS; DIET, HIGH-FAT; GENE EXPRESSION; INSULIN; LIPOGENESIS; LIVER; MALE; MICE; MICE, INBRED ICR; ORGAN SIZE; TRANSCRIPTION FACTORS;

EID: 84960360268     PISSN: 00260495     EISSN: 15328600     Source Type: Journal    
DOI: 10.1016/j.metabol.2015.12.003     Document Type: Article

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