Key result
Expression of soluble epoxide hydrolase (sEH) proteins and treatment with fatty acid epoxides and diols demonstrated a cholesterol-lowering effect in mammalian cell lines.
Why the study?
Does soluble epoxide hydrolase (sEH) expression or treatment with sEH-related compounds lower cholesterol levels in mammalian cells?
Does soluble epoxide hydrolase (sEH) expression or treatment with sEH-related compounds lower cholesterol levels in mammalian cells?
Soluble epoxide hydrolase and related fatty acid epoxides and diols demonstrate cholesterol-lowering effects in mammalian cells, highlighting a novel pathway in cholesterol regulation.
Should not change lipid management; hypothesis-generating for sEH in cholesterol regulation.
Soluble epoxide hydrolase (sEH) is becoming an attractive therapeutic target in cardiovascular disease. Recently, known human sEH polymorphisms were associated with elevated plasma cholesterol and atherosclerosis. In this study we evaluated the potential role of sEH in regulating cholesterol metabolism through modulating the levels of fatty acid epoxide substrates and/or their corresponding diol products known to activate peroxisome proliferator activated receptors (PPARs). We measured changes in cholesterol levels induced by expressing sEH proteins in mammalian cell lines and in response to treatment with various sEH-related compounds. Our results indicate that sEH has a cholesterol lowering effect that is mediated at least in part through its C-terminal hydrolase activity. In addition, several fatty acid epoxides and their corresponding diols showed cholesterol lowering effects in the current study. In conclusion, this study provides evidence that fatty acid epoxides and diols are endogenous cholesterol lowering molecules and that sEH may be involved in cholesterol regulation by modulating their levels.
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Enayetallah et al. (2007) studied Cholesterol metabolism. Expression of sEH proteins and treatment with sEH-related compounds was evaluated on Changes in cholesterol levels. Expression of soluble epoxide hydrolase (sEH) proteins and treatment with fatty acid epoxides and diols demonstrated a cholesterol-lowering effect in mammalian cell lines.
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