MK-0767, a novel dual PPARalpha/gamma agonist, displays robust antihyperglycemic and hypolipidemic activities

Biochem Biophys Res Commun. 2004 May 28;318(2):323-8. doi: 10.1016/j.bbrc.2004.04.032.

Abstract

Here, we characterize the actions of MK-0767, a dual ligand of the nuclear receptors peroxisome proliferator-activated receptor (PPAR)alpha and PPARgamma. In cell-based assays, MK-0767 produced potent activation of human PPARgamma and PPARalpha with a gamma:alpha potency ratio of approximately 2. The dual agonist induced high affinity interactions of PPARalpha and PPARgamma with the transcriptional coactivator CBP in vitro. In ob/ob mice, MK-0767 normalized hyperglycemia and hyperinsulinemia with equal or greater potency and efficacy than pioglitazone. Treatment of hamsters with MK-0767 produced substantial reductions in blood cholesterol and triglycerides. In dogs, MK-0767 reduced serum cholesterol levels with a potency more than 10-fold greater than simvastatin. The efficacies of MK-0767 and simvastatin were additive when given together. We conclude that MK-0767 is a potent dual PPARalpha/gamma agonist with robust insulin sensitizing and hypolipidemic activities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzamides / chemistry
  • Benzamides / pharmacology*
  • Blood Glucose / analysis
  • COS Cells
  • Chlorocebus aethiops
  • Cholesterol / blood
  • Cricetinae
  • Dogs
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Female
  • Humans
  • Hypoglycemic Agents / chemistry
  • Hypoglycemic Agents / pharmacology*
  • Hypolipidemic Agents / chemistry
  • Hypolipidemic Agents / pharmacology*
  • Insulin / blood
  • Male
  • Mesocricetus
  • Mice
  • Mice, Obese
  • Pioglitazone
  • Receptors, Cytoplasmic and Nuclear / agonists*
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Simvastatin / pharmacology
  • Thiazoles / pharmacology*
  • Thiazolidinediones / pharmacology
  • Trans-Activators / metabolism
  • Transcription Factors / agonists*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcriptional Activation / drug effects
  • Triglycerides / blood

Substances

  • Benzamides
  • Blood Glucose
  • Hypoglycemic Agents
  • Hypolipidemic Agents
  • Insulin
  • MK0767
  • Receptors, Cytoplasmic and Nuclear
  • Thiazoles
  • Thiazolidinediones
  • Trans-Activators
  • Transcription Factors
  • Triglycerides
  • Cholesterol
  • Simvastatin
  • Pioglitazone