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. 2020 Aug 17;20:257. doi: 10.1186/s12906-020-03052-w

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 6 — The effect on regulating cholesterol disorders and mechanism of quercetin on the HepG2 cells induced by LDL for 24 h. a-c Expression of SREBP2 and HMGCR protein were analyzed by western blotting. d Expression of SREBP2 and HMGCR protein were analyzed by immunofluorescence assay. Control: control group; LDL: a high cholesterol level simulation model of HepG2 cells by low density lipoprotein (25 μg ml^− 1); LDL + Que.: quercetin with LDL model HepG2 cells (30, 10 μmol l^− 1). Data were presented as mean ± SEM. n = 6, *p < 0.05, **p < 0.01, ***p < 0.001 vs. control group