HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Dietary camphene attenuates hepatic steatosis and insulin resistance in mice.

AbstractOBJECTIVE:
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:
Camphene alleviated the HFD-induced increases in liver weight and hepatic lipid levels in mice. Camphene also increased circulating adiponectin levels. To examine the direct effects of camphene on adiponectin secretion, 3T3-L1 adipocytes were incubated with camphene. Consistent with in vivo result, camphene increased adiponectin expression and secretion in 3T3-L1 adipocytes. In HFD-fed mice, camphene increased hepatic adiponectin receptor expression and AMP-activated protein kinase (AMPK) activation. Concordant with the activation of adiponectin-AMPK signaling, camphene increased hepatic expression of fatty acid oxidation-related genes and decreased those of lipogenesis-related genes in HFD-fed mice. Moreover, camphene increased insulin-signaling molecules activation and stimulated glucose transporter-2translocation to the plasma membrane in the liver.
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.
AuthorsSohee Kim, Youngshim Choi, Seoyoon Choi, Yeji Choi, Taesun Park
JournalObesity (Silver Spring, Md.) (Obesity (Silver Spring)) Vol. 22 Issue 2 Pg. 408-17 (Feb 2014) ISSN: 1930-739X [Electronic] United States
PMID23818423 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 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
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)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: