Romano, Adele;
Friuli, Marzia;
Del Coco, Laura;
Longo, Serena;
Vergara, Daniele;
Del Boccio, Piero;
Valentinuzzi, Silvia;
Cicalini, Ilaria;
Fanizzi, Francesco P.;
Gaetani, Silvana;
Giudetti, Anna M.
Chronic Oleoylethanolamide Treatment Decreases Hepatic Triacylglycerol Level in Rat Liver by a PPARγ/SREBP-Mediated Suppression of Fatty Acid and Triacylglycerol Synthesis
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Medientyp:
E-Artikel
Titel:
Chronic Oleoylethanolamide Treatment Decreases Hepatic Triacylglycerol Level in Rat Liver by a PPARγ/SREBP-Mediated Suppression of Fatty Acid and Triacylglycerol Synthesis
Beteiligte:
Romano, Adele;
Friuli, Marzia;
Del Coco, Laura;
Longo, Serena;
Vergara, Daniele;
Del Boccio, Piero;
Valentinuzzi, Silvia;
Cicalini, Ilaria;
Fanizzi, Francesco P.;
Gaetani, Silvana;
Giudetti, Anna M.
Beschreibung:
<jats:p>Oleoylethanolamide (OEA) is a naturally occurring bioactive lipid belonging to the family of N-acylethanolamides. A variety of beneficial effects have been attributed to OEA, although the greater interest is due to its potential role in the treatment of obesity, fatty liver, and eating-related disorders. To better clarify the mechanism of the antiadipogenic effect of OEA in the liver, using a lipidomic study performed by 1H-NMR, LC-MS/MS and thin-layer chromatography analyses we evaluated the whole lipid composition of rat liver, following a two-week daily treatment of OEA (10 mg kg−1 i.p.). We found that OEA induced a significant reduction in hepatic triacylglycerol (TAG) content and significant changes in sphingolipid composition and ceramidase activity. We associated the antiadipogenic effect of OEA to decreased activity and expression of key enzymes involved in fatty acid and TAG syntheses, such as acetyl-CoA carboxylase, fatty acid synthase, diacylglycerol acyltransferase, and stearoyl-CoA desaturase 1. Moreover, we found that both SREBP-1 and PPARγ protein expression were significantly reduced in the liver of OEA-treated rats. Our findings add significant and important insights into the molecular mechanism of OEA on hepatic adipogenesis, and suggest a possible link between the OEA-induced changes in sphingolipid metabolism and suppression of hepatic TAG level.</jats:p>