过氧化物酶体增殖物激活受体
氯贝特酸
脂质代谢
过氧化物酶体
新陈代谢
过氧化物酶体增殖物激活受体α
氨基酸
化学
受体
生物
生物化学
核受体
内科学
转录因子
内分泌学
基因
医学
作者
Sander Kersten,Stéphane Mandard,Pascal Escher,Frank J. Gonzalez,Sherrie Tafuri,Béatrice Desvergne,Walter Wahli
标识
DOI:10.1096/fj.01-0147com
摘要
The peroxisome proliferator‐activated receptor α is a ligand‐activated transcription factor that plays an important role in the regulation of lipid homeostasis. PPARα mediates the effects of fibrates, which are potent hypolipidemic drugs, on gene expression. To better understand the biological effects of fibrates and PPARα, we searched for genes regulated by PPARα using oligonucleotide microarray and sub‐tractive hybridization. By comparing liver RNA from wild‐type and PPARα null mice, it was found that PPARα decreases the mRNA expression of enzymes involved in the metabolism of amino acids. Further analysis by Northern blot revealed that PPARα influences the expression of several genes involved in transand deamination of amino acids, and urea synthesis. Direct activation of PPARα using the synthetic PPARα ligand WY14643 decreased mRNA levels of these genes, suggesting that PPARα is directly implicated in the regulation of their expression. Consistent with these data, plasma urea concentrations are modulated by PPARα in vivo. It is concluded that in addition to oxidation of fatty acids, PPARα also regulates metabolism of amino acids in liver, indicating that PPARα is a key controller of intermediary metabolism during fasting.
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