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J Lipid Res ; 42(11): 1831-40, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11714852

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.


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