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. 2020 Mar;8(5):231. doi: 10.21037/atm.2020.01.31

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2020 Annals of Translational Medicine. All rights reserved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0.

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Figure S2 — mRNA levels of genes related to fatty acid synthesis, β-oxidation, bile acid and cholesterol metabolism in liver. (A) 3-hydroxy-3-methylglutaryl CoA reductase (Hmgcr), (B) fatty acid binding protein 1 (Fabp1), (C) long chain acyl-CoA dehydrogenase (Lcad), (D) lipoprotein lipase (Lpl), (E) Cholesterol 7a-hydroxylase (Cyp7a1), (F) Cytochrome P450 Family 2 Subfamily E Member 1(CYP2E1), and (G) peroxisome proliferation-activated receptor (PPAR)-α levels were analysed by qRT-PCR. The values were presented as mean ± S.E.M. (n=6 per group). Graph bars with different letters on top represent statistically significant results (P<0.05) based on Newman-Keuls post hoc one-way ANOVA analysis, whereas bars with the same letter correspond to results that show no statistically significant differences.