» Articles » PMID: 28169366

Phytosterol Esters Attenuate Hepatic Steatosis in Rats with Non-alcoholic Fatty Liver Disease Rats Fed a High-fat Diet

Overview
Journal Sci Rep
Specialty Science
Date 2017 Feb 8
PMID 28169366
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Given the adverse effects of drugs used for NAFLD treatment, identifying novel and effective natural compound to prevent NAFLD is urgently needed. In the present study, the effects of phytosterol esters (PSEs) on NAFLD were explored. Adult SD rats were randomized into five groups: normal chow diet (NC), high-fat diet (HF), low-, medium- and high-dose PSE treatment plus high-fat diet groups (PSEL, PSEM, and PSEH). Our results showed that the levels of LDL-C in the PSEL group and hepatic TG, TC, and FFA in the three PSEs groups were significantly decreased. Notably, the uric acid (UA) level was significantly decreased by PSEs intervention. The hepatic inflammatory stress was ameliorated via the inhibition of the cytokines, including TGF-β, IL-6, IL-10 and CRP in the PSEs intervention groups. Further, the oxidative status was improved by PSE treatment through adjusting the enzyme activity (SOD and XOD) and decreasing the MDA level. These beneficial effects of PSE may have been partly due to its regulation on the expression of TGF-β1, TGF-β2, TNF-α, UCP-2, PPAR-α and PPAR-γ in hepatic tissue at both mRNA and protein level. The results of this study suggest that PSEs may be used as therapeutic agents for the prevention and progression of NAFLD and that hyperuricemia is induced by high-fat diet consumption.

Citing Articles

Submicron Dispersions of Phytosterols Reverse Liver Steatosis with Higher Efficacy than Phytosterol Esters in a Diet Induced-Fatty Liver Murine Model.

Gillet R, Cerda-Drago T, Branes M, Valenzuela R Int J Mol Sci. 2025; 26(2).

PMID: 39859279 PMC: 11766071. DOI: 10.3390/ijms26020564.


Metabolic dysfunction-associated steatotic liver disease-induced changes in the antioxidant system: a review.

Svobodova G, Horni M, Velecka E, Bousova I Arch Toxicol. 2024; 99(1):1-22.

PMID: 39443317 PMC: 11748479. DOI: 10.1007/s00204-024-03889-x.


Effects of Chronic Sleep Restriction on Transcriptional Sirtuin 1 Signaling Regulation in Male Mice White Adipose Tissue.

Rendine M, Cocci P, de Vivo L, Bellesi M, Palermo F Curr Issues Mol Biol. 2024; 46(3):2144-2154.

PMID: 38534754 PMC: 10969409. DOI: 10.3390/cimb46030138.


Unsaponifiable Matter from Wheat Bran Cultivated in Korea Inhibits Hepatic Lipogenesis by Activating AMPK Pathway.

An M, Heo H, Park J, Jeong H, Kim Y, Lee J Foods. 2023; 12(21).

PMID: 37959135 PMC: 10650137. DOI: 10.3390/foods12214016.


β-sitosterol attenuates high- fat diet-induced hepatic steatosis in rats by modulating lipid metabolism, inflammation and ER stress pathway.

Abo-Zaid O, Moawed F, Ismail E, Farrag M BMC Pharmacol Toxicol. 2023; 24(1):31.

PMID: 37173727 PMC: 10182633. DOI: 10.1186/s40360-023-00671-0.


References
1.
Ratziu V, Bellentani S, Cortez-Pinto H, Day C, Marchesini G . A position statement on NAFLD/NASH based on the EASL 2009 special conference. J Hepatol. 2010; 53(2):372-84. DOI: 10.1016/j.jhep.2010.04.008. View

2.
Gressner A, Weiskirchen R, Breitkopf K, Dooley S . Roles of TGF-beta in hepatic fibrosis. Front Biosci. 2002; 7:d793-807. DOI: 10.2741/A812. View

3.
Angulo P, Keach J, Batts K, Lindor K . Independent predictors of liver fibrosis in patients with nonalcoholic steatohepatitis. Hepatology. 1999; 30(6):1356-62. DOI: 10.1002/hep.510300604. View

4.
Provenzano A, Milani S, Vizzutti F, Delogu W, Navari N, Novo E . n-3 polyunsaturated fatty acids worsen inflammation and fibrosis in experimental nonalcoholic steatohepatitis. Liver Int. 2014; 34(6):918-30. DOI: 10.1111/liv.12500. View

5.
Saggiani F, Pilati S, Targher G, Branzi P, Muggeo M, Bonora E . Serum uric acid and related factors in 500 hospitalized subjects. Metabolism. 1996; 45(12):1557-61. DOI: 10.1016/s0026-0495(96)90188-2. View