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Linseed Oil Attenuates Liver Inflammation, Fatty Acid Accumulation, and Lipid Distribution in Periportal and Perivenous Hepatocytes Induced by a High-Carbohydrate Diet in Mice.

Guilherme GodoyMarina Masetto AntunesIngrid de Lima FernandesLuciana Pelissari ManinCaroline ZappieloLaureane Nunes MasiJuliana Vanessa Colombo Martins PerlesJesuí Vergílio VisentainerRui CuriRoberto Barbosa Bazotte
Published in: Journal of medicinal food (2022)
We evaluated whether linseed oil (LO) modulates the effects of a high-carbohydrate diet (HCD) on liver inflammation, fatty acid (FA) accumulation, and lipid distribution in periportal and perivenous hepatocytes. The control group (control high-carbohydrate diet [HCD-C]) received an HCD with lard and soybean oil as the lipid source. The L10 and L100 groups received the HCD with 10% and 100% of LO as the lipid source, respectively. The animals were killed by decapitation before (day 0) and after receiving the diets. Liver FA composition, inflammation, and fibrogenesis gene expression were evaluated. Also, the percentage of lipid-occupied area in periportal end perivenous hepatocytes were measured. The L100 group exhibited a higher ( P  < .05) liver amount of omega-3 polyunsaturated FA (n-3 PUFA) and lower ( P  < .05) amounts of saturated FA (SFA), monounsaturated FA (MUFA), and omega-6 polyunsaturated FA (n-6 PUFA) compared with L10 or HCD-C mice. On day 56, interleukin 10 and type IV collagen gene expression were significantly upregulated and downregulated, respectively in L100. Also, the L100 group showed lower ( P  < .05) FA accumulation ( i.e ., total FA, SFA, MUFA, and n-6 PUFA). Also, L10 and L100 presented lower ( P  < .05) percentage of high lipid-containing portion in periportal and perivenous hepatocytes. We concluded that LO attenuation of liver inflammation promoted by an HCD is associated with increased liver n-3 PUFA levels, so modulating FA composition, deposition, and distribution in periportal and perivenous hepatocytes.
Keyphrases
  • fatty acid
  • gene expression
  • oxidative stress
  • weight loss
  • liver injury
  • physical activity
  • dna methylation
  • signaling pathway
  • drug induced
  • type diabetes
  • skeletal muscle
  • high fat diet induced