PPARalpha suppresses insulin secretion and induces UCP2 in insulinoma cells

J Lipid Res. 2002 Jun;43(6):936-43.

Abstract

Fatty acids may promote type 2 diabetes by altering insulin secretion from pancreatic beta cells, a process known as lipotoxicity. The underlying mechanisms are poorly understood. To test the hypothesis that peroxisome proliferator-activated receptor alpha (PPARalpha) has a direct effect on islet function, we treated INS-1 cells, an insulinoma cell line, with a PPARalpha adenovirus (AdPPARalpha) as well as the PPARalpha agonist clofibric acid. AdPPARalpha-infected INS-1 cells showed PPARalpha agonist- and fatty acid-dependent transactivation of a PPARalpha reporter gene. Treatment with either AdPPARalpha or clofibric acid increased both catalase activity (a marker of peroxisomal proliferation) and palmitate oxidation. AdPPARalpha induced carnitine-palmitoyl transferase-I (CPT-I) mRNA, but had no effect on insulin gene expression. AdPPARalpha treatment increased cellular triglyceride content but clofibric acid did not. Both AdPPARalpha and clofibric acid decreased basal and glucose-stimulated insulin secretion. Despite increasing fatty acid oxidation, AdPPARalpha did not increase cellular ATP content suggesting the stimulation of uncoupled respiration. Consistent with these observations, UCP2 expression doubled in PPARalpha-treated cells. Clofibric acid-induced suppression of glucose-simulated insulin secretion was prevented by the CPT-I inhibitor etomoxir. These data suggest that PPARalpha-stimulated fatty acid oxidation can impair beta cell function.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adenoviridae
  • Animals
  • Catalase / metabolism
  • Clofibric Acid / metabolism
  • Epoxy Compounds / metabolism
  • Fatty Acids / metabolism
  • Genetic Vectors
  • Glucose / metabolism
  • Insulin / metabolism*
  • Insulin Secretion
  • Insulinoma / metabolism*
  • Ion Channels
  • Membrane Transport Proteins*
  • Mice
  • Mitochondrial Proteins*
  • Protein Biosynthesis*
  • Rats
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / physiology*
  • Transcription Factors / genetics
  • Transcription Factors / physiology*
  • Triglycerides / metabolism
  • Tumor Cells, Cultured
  • Uncoupling Protein 2

Substances

  • Epoxy Compounds
  • Fatty Acids
  • Insulin
  • Ion Channels
  • Membrane Transport Proteins
  • Mitochondrial Proteins
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Triglycerides
  • Ucp2 protein, mouse
  • Ucp2 protein, rat
  • Uncoupling Protein 2
  • Clofibric Acid
  • Adenosine Triphosphate
  • Catalase
  • Glucose
  • etomoxir