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Fargesin improves lipid and glucose metabolism in 3T3-L1 adipocytes and high-fat diet-induced obese mice.

Abstract
This study examined the effects of fargesin, a neolignan isolated from Magnolia plants, on obesity and insulin resistance and the possible mechanisms involved in these effects in 3T3-L1 adipocytes and high-fat diet (HFD)-induced obese mice. Fargesin promoted the glucose uptake in 3T3-L1 adipocytes. In HFD-induced obese mice, fargesin decreased the body weight gain, white adipose tissue (WAT), and plasma triglyceride, non-esterified fatty acid and glucose levels, and improved the glucose tolerance. Fargesin increased glucose transporter 4 (GLUT4) protein expression and phosphorylation of Akt, AMP-activated protein kinase (AMPK), and acetyl-CoA carboxylase (ACC) in both 3T3-L1 adipocytes and WAT of HFD-induced obese mice. Fargesin also decreased the mRNA expression levels of fatty acid oxidation-related genes, such as peroxisome proliferator-activated receptor α (PPARα), carnitine palmitoyltransferase-1 (CPT-1), uncoupling protein-2 (UCP-2) and leptin in WAT. Taken together, the present findings suggest that fargesin improves dyslipidemia and hyperglycemia by activating Akt and AMPK in WAT.
AuthorsYoung-Sil Lee, Byung-Yoon Cha, Sun-Sil Choi, Yumiko Harada, Bong-Keun Choi, Takayuki Yonezawa, Toshiaki Teruya, Kazuo Nagai, Je-Tae Woo
JournalBioFactors (Oxford, England) (Biofactors) 2012 Jul-Aug Vol. 38 Issue 4 Pg. 300-8 ISSN: 1872-8081 [Electronic] Netherlands
PMID22674784 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 International Union of Biochemistry and Molecular Biology, Inc.
Chemical References
  • Benzodioxoles
  • Blood Glucose
  • Glucose Transporter Type 4
  • Hypoglycemic Agents
  • Hypolipidemic Agents
  • Lignans
  • Lipids
  • Slc2a4 protein, mouse
  • Proto-Oncogene Proteins c-akt
  • Adenylate Kinase
  • Acetyl-CoA Carboxylase
  • fargesin
  • Glucose
Topics
  • 3T3-L1 Cells
  • Acetyl-CoA Carboxylase (metabolism)
  • Adenylate Kinase (metabolism)
  • Adipocytes (drug effects, metabolism)
  • Animals
  • Benzodioxoles (pharmacology, therapeutic use)
  • Blood Glucose
  • Diet, High-Fat (adverse effects)
  • Gene Expression (drug effects)
  • Glucose (metabolism)
  • Glucose Transporter Type 4 (metabolism)
  • Hypoglycemic Agents (pharmacology, therapeutic use)
  • Hypolipidemic Agents (pharmacology, therapeutic use)
  • Lignans (pharmacology, therapeutic use)
  • Lipid Metabolism (drug effects)
  • Lipids (blood)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • Obesity (drug therapy, etiology, metabolism)
  • Organ Size (drug effects)
  • Phosphorylation
  • Protein Processing, Post-Translational
  • Proto-Oncogene Proteins c-akt (metabolism)
  • Weight Gain (drug effects)

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