PPARalpha deficiency increases secretion and serum levels of apolipoprotein B-containing lipoproteins

J Lipid Res. 2001 Nov;42(11):1831-40.

Abstract

This study investigates the importance of peroxisome proliferator activated receptor alpha (PPARalpha) for serum apolipoprotein B (apoB) levels and hepatic secretion of apoB-containing lipoproteins. Total serum apoB and VLDL-apoB levels were higher in female PPARalpha-null mice compared with female wild-type mice, but no difference was seen in male mice. Furthermore, hepatic triglyceride secretion rate, determined in vivo after Triton WR1339 injection, was 2.4-fold higher in female PPARalpha-null mice compared with female wild-type mice, but no difference was observed in male mice. However, when fed a high fat diet, male PPARalpha-null mice displayed 2-fold higher serum levels of apoB and LDL cholesterol compared with male wild-type mice, but triglyceride levels were not affected. Hepatic LDL receptor protein levels were not influenced by PPARalpha deficiency, gender, or the fat diet. Hepatocyte cultures from female PPARalpha-null mice (cultured for 4 days in serum free medium) showed 2-fold higher total apoB secretion and increased secretion of apoB-48 VLDL, as well as 2.7-fold larger accumulation of VLDL-triglycerides in the medium compared with wild-type cultures. In conclusion, PPARalpha-deficient female mice, but not males, display high serum apoB associated with VLDL and increased hepatic triglyceride secretion. Moreover, male PPARalpha-null mice show increased susceptibility to high fat diet in terms of serum apoB levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apolipoproteins B / blood*
  • Apolipoproteins B / genetics
  • Apolipoproteins B / metabolism*
  • Blotting, Western
  • Cells, Cultured
  • Cholesterol / blood
  • Cholesterol, LDL / blood
  • Dietary Fats / administration & dosage
  • Lipoproteins / blood*
  • Lipoproteins / metabolism*
  • Lipoproteins, VLDL / blood
  • Lipoproteins, VLDL / metabolism
  • Liver / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • RNA, Messenger / analysis
  • Receptors, Cytoplasmic and Nuclear / deficiency*
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, LDL / analysis
  • Transcription Factors / deficiency*
  • Transcription Factors / genetics
  • Triglycerides / blood

Substances

  • Apolipoproteins B
  • Cholesterol, LDL
  • Dietary Fats
  • Lipoproteins
  • Lipoproteins, VLDL
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, LDL
  • Transcription Factors
  • Triglycerides
  • Cholesterol