Abstract | OBJECTIVE: The aim of this study was to investigate the protective effects of camphene on high-fat diet (HFD)-induced hepatic steatosis and insulin resistance in mice and to elucidate its mechanism of action. DESIGN AND METHODS: Male C57BL/6N mice were fed with a normal diet, HFD (20% fat and 1% cholesterol of total diet), or HFD supplemented with 0.2% camphene (CPND) for 10 weeks. RESULTS: CONCLUSIONS: These results suggest camphene prevents HFD-induced hepatic steatosis and insulin resistance in mice; furthermore, these protective effects are mediated via the activation of adiponectin-AMPK signaling.
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Authors | Sohee Kim, Youngshim Choi, Seoyoon Choi, Yeji Choi, Taesun Park |
Journal | Obesity (Silver Spring, Md.)
(Obesity (Silver Spring))
Vol. 22
Issue 2
Pg. 408-17
(Feb 2014)
ISSN: 1930-739X [Electronic] United States |
PMID | 23818423
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 The Obesity Society. |
Chemical References |
- Adiponectin
- Adipoq protein, mouse
- Antioxidants
- Bicyclic Monoterpenes
- Receptors, Adiponectin
- Terpenes
- adiponectin receptor 1, mouse
- adiponectin receptor 2, mouse
- AMP-Activated Protein Kinases
- camphene
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Topics |
- 3T3-L1 Cells
- AMP-Activated Protein Kinases
(chemistry, metabolism)
- Adipocytes, White
(metabolism, pathology)
- Adipogenesis
- Adiponectin
(agonists, genetics, metabolism)
- Animals
- Antioxidants
(metabolism, therapeutic use)
- Bicyclic Monoterpenes
- Dietary Supplements
- Enzyme Activation
- Fatty Liver
(metabolism, pathology, physiopathology, prevention & control)
- Gene Expression Regulation
- Insulin Resistance
- Liver
(metabolism, pathology, physiopathology)
- Male
- Mice
- Mice, Inbred C57BL
- Organ Size
- Random Allocation
- Receptors, Adiponectin
(agonists, genetics, metabolism)
- Signal Transduction
- Terpenes
(metabolism, therapeutic use)
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