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Comparison of the Effects of Cholesterol, Palmitic Acid, and Glucose on Activation of Human Hepatic Stellate Cells to Induce Liver Fibrosis

Overview
Specialty Endocrinology
Date 2022 Nov 21
PMID 36404864
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Abstract

Background: In hepatic damage, Hepatic stellate cells (HSCs) become active, proliferate, and change to myofibroblasts. Increasing the fibrogenic genes, such as Transforming growth factor-β (TGF-β), Alpha Smooth Muscle Actin (α-SMA), and Collagen1 α (COL 1α) show that the activation of HSCs can lead to hepatic fibrosis.

Purpose: These days people consume much cholesterol, palmitic acid, and glucose which can have adverse effects on an individuals' health, but their influences on activating human HSCs and inducing liver fibrosis have not been assessed. Our purpose is to investigate the effects of these three main and abundant ingredients in the diet on the activation of human HSCs and inducing liver fibrosis.

Methods: To measure cholesterol, palmitic acid, and glucose cytotoxic effects on the viability of the cells, the MTT technique was used. Then the treated cells were incubated in media containing cholesterol, palmitic acid, and glucose with different concentrations for 24 h. At last, the α-SMA, COL 1α, and TGF-β, genes mRNA expression were measured by real-time PCR.

Results And conclusions: Our results demonstrated that high concentrations of cholesterol and palmitic acid can activate human HSCs that lead to an increase in the mRNA expressions of fibrogenic genes. Thus, controlling fat intaking and knowing its mechanism is crucial to prevent and attenuate hepatic fibrosis.

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References
1.
Wells R . The role of matrix stiffness in hepatic stellate cell activation and liver fibrosis. J Clin Gastroenterol. 2005; 39(4 Suppl 2):S158-61. DOI: 10.1097/01.mcg.0000155516.02468.0f. View

2.
Liu X, Hu H, Yin J . Therapeutic strategies against TGF-beta signaling pathway in hepatic fibrosis. Liver Int. 2006; 26(1):8-22. DOI: 10.1111/j.1478-3231.2005.01192.x. View

3.
Liu Z, Li C, Kang N, Malhi H, Shah V, Maiers J . Transforming growth factor β (TGFβ) cross-talk with the unfolded protein response is critical for hepatic stellate cell activation. J Biol Chem. 2019; 294(9):3137-3151. PMC: 6398135. DOI: 10.1074/jbc.RA118.005761. View

4.
Krizhanovsky V, Yon M, Dickins R, Hearn S, Simon J, Miething C . Senescence of activated stellate cells limits liver fibrosis. Cell. 2008; 134(4):657-67. PMC: 3073300. DOI: 10.1016/j.cell.2008.06.049. View

5.
Kiss K, Regos E, Rada K, Firneisz G, Baghy K, Kovalszky I . Chronic Hyperglycaemia Induced Alterations of Hepatic Stellate Cells Differ from the Effect of TGFB1, and Point toward Metabolic Stress. Pathol Oncol Res. 2018; 26(1):291-299. DOI: 10.1007/s12253-018-0458-9. View