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. 2022 Sep 24;21:91. doi: 10.1186/s12944-022-01698-8

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© The Author(s) 2022

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. 3 — Effect of EPL, PPC and PI on hepatocellular transport protein activity in HepG2 cell line. Values shown are mean ± SE (cellular substrate accumulation as percentage of untreated cells) for 4 (MRP-2, BSEP, P-GP) or 5 (BCRP) experiments; n = 1 (BCRP), 4 (MRP-2, BSEP) or 6 (P-GP) wells for each concentration of each compound/experiment. ns: not significant; ***P < 0.001 versus untreated cells. BCRP, breast cancer resistance protein; BSEP, bile salt export protein; EPL, essential phospholipids; MRP-2, multidrug resistance-associated protein 2; P-GP, P-glycoprotein; PI, phosphatidylinositol; PPC, polyenylphosphatidylcholine; SE, standard error. Supplementary Table S6 shows the statistical analyses