Artículos de revistas
Iron-induced derangement in hepatic Delta-5 and Delta-6 desaturation capacity and fatty acid profile leading to steatosis: Impact on extrahepatic tissues and prevention by antioxidant-rich extra virgin olive oil
Fecha
2020Registro en:
Barrera, C., Valenzuela, R., Rincón, M. A., Espinosa, A., López-Arana, S., González-Mañan, D., ... & Videla, L. A. (2020). Iron-induced derangement in hepatic Δ-5 and Δ-6 desaturation capacity and fatty acid profile leading to steatosis: Impact on extrahepatic tissues and prevention by antioxidant-rich extra virgin olive oil. Prostaglandins, Leukotrienes and Essential Fatty Acids, 153, 102058.
0952-3278
1532-2823
DOI: 10.1016/j.plefa.2020.102058
Autor
González-Manan, Daniel [Univ Mayor, Fac Ciencias, Nucleo Quim & Bioquim]
Barrera, Cynthia
Valenzuela, Rodrigo
Rincon, Miguel A.
Espinosa, Alejandra
López-Arana, Sandra
Romero, Nalda
Vargas, Romina
Videla, Luis A.
Institución
Resumen
The administration of iron induces liver oxidative stress and depletion of long-chain polyunsaturated fatty acids (LCPUFAs), n-6/n-3 LCPUFA ratio enhancement and fat accumulation, which may be prevented by antioxidant-rich extra virgin olive oil (AR-EVOO) supplementation. Male Wistar rats were subjected to a control diet (50 mg iron/kg diet) or iron-rich diet (IRD; 200 mg/kg diet) with alternate AR-EVOO for 21 days. Liver fatty acid (FA) analysis was performed by gas-liquid chromatography (GLC) after lipid extraction and fractionation, besides Delta-5 desaturase (Delta-5 D) and Delta 6-D mRNA expression (qPCR) and activity (GLC) measurements. The IRD significantly (p < 0.05) increased hepatic total fat, triacylglycerols, free FA contents and serum transaminases levels, with diminution in those of n-6 and n-3 LCPUFAs, higher n-6/n-3 ratios, lower unsaturation index and Delta 5-D and Delta 6-D activities, whereas the mRNA expression of both desaturases was enhanced over control values, changes that were prevented by concomitant AR-EVOO supplementation. N-6 and n-3 LCPUFAs were also decreased by IRD in extrahepatic tissues and normalized by AR-EVOO. In conclusion, AR-EVOO supplementation prevents IRD-induced changes in parameters related to liver FA metabolism and steatosis, an effect that may have a significant impact in the treatment of iron-related pathologies or metabolic disorders such as non-alcoholic fatty liver disease.