Title : Nonalcoholic fatty liver disease impairs the cytochrome P-450-dependent metabolism of α-tocopherol (vitamin E).

Pub. Date : 2017 Sep

PMID : 28628909






4 Functional Relationships(s)
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1 CYP4F2 protein, a cytochrome P-450 isoform with proposed alpha-tocopherol omega-hydroxylase activity, decreased in HFD and even more in HFD+F mice liver; this finding was associated with increased hepatic levels of alpha-tocopherol and decreased formation of the corresponding long-chain metabolites alpha-13-hydroxy and alpha-13-carboxy chromanols. alpha-Tocopherol cytochrome P450 family 4 subfamily F member 2 Homo sapiens
2 CYP4F2 protein, a cytochrome P-450 isoform with proposed alpha-tocopherol omega-hydroxylase activity, decreased in HFD and even more in HFD+F mice liver; this finding was associated with increased hepatic levels of alpha-tocopherol and decreased formation of the corresponding long-chain metabolites alpha-13-hydroxy and alpha-13-carboxy chromanols. alpha-Tocopherol cytochrome P450 family 4 subfamily F member 2 Homo sapiens
3 A transient activation of CYP4F2 gene followed by a repression response was observed in HepG2 cells during the exposure to increasing levels of the lipogenic and cytotoxic agent palmitic acid; such gene repression effect was further exacerbated by the co-treatment with oleic acid and alpha-tocopherol and was also observed for PPAR-gamma and the SREBP isoforms 1 and 2. alpha-Tocopherol cytochrome P450 family 4 subfamily F member 2 Homo sapiens
4 Such gene response was associated with increased uptake and omega-hydroxylation of alpha-tocopherol, which suggests a minor role of CYP4F2 in the enzymatic metabolism of vitamin E in HepG2 cells. alpha-Tocopherol cytochrome P450 family 4 subfamily F member 2 Homo sapiens