C333H, a novel PPARalpha/gamma dual agonist, has beneficial effects on insulin resistance and lipid metabolism

Acta Pharmacol Sin. 2006 Feb;27(2):223-8. doi: 10.1111/j.1745-7254.2006.00263.x.

Abstract

Aim: To examine the effects of novel peroxisome proliferator-activated receptor (PPAR) alpha/gamma dual agonist C333H on insulin resistance and lipid metabolism.

Methods: An established dual-luciferase reporter gene assay system was used in vitro to test the activity of C333H with respect to the transcription of human PPARalpha and PPARgamma. A preadipocyte differentiation assay and reverse transcription-polymerase chain reaction were used to detect the functional activities of C333H. In db/db mice, the effects of C333H were investigated with respect to lowering of blood glucose and lipid levels.

Results: C333H was determined to be a novel PPARalpha/gamma dual agonist because it strongly induced luciferase activity on human PPARalpha and PPARgamma, promoting the differentiation of preadipocytes to adipocytes, and functioning in upregulating the expression of some glucose and lipid metabolic target genes of the PPAR. In addition, C333H efficiently reduced blood lipid and glucose concentrations in db/db diabetic mice.

Conclusion: C333H has dual action on both PPARalpha and PPARgamma, and might be of interest for the amelioration of lipid metabolic disorders and insulin resistance associated with type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology
  • Adipocytes / metabolism
  • Animals
  • Blood Glucose / metabolism
  • Cell Differentiation
  • Cell Line
  • Cholesterol / blood
  • Diabetes Mellitus, Type 2 / blood
  • Fatty Acids, Nonesterified / blood
  • Furans / pharmacology*
  • Glucose Transporter Type 4 / biosynthesis
  • Glucose Transporter Type 4 / genetics
  • Hepatocytes / cytology
  • Hepatocytes / metabolism
  • Humans
  • Insulin Resistance*
  • Lipid Metabolism / drug effects*
  • Lipoprotein Lipase / biosynthesis
  • Lipoprotein Lipase / genetics
  • Male
  • Mice
  • Oxazoles / pharmacology*
  • PPAR alpha / agonists*
  • PPAR gamma / agonists*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Triglycerides / blood

Substances

  • Blood Glucose
  • C333H compound
  • Fatty Acids, Nonesterified
  • Furans
  • Glucose Transporter Type 4
  • Oxazoles
  • PPAR alpha
  • PPAR gamma
  • RNA, Messenger
  • Triglycerides
  • Cholesterol
  • Lipoprotein Lipase