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. 2022 Jul 25;12:12630. doi: 10.1038/s41598-022-17038-w

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© The Author(s) 2022

Open Access This 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/.

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Effects of extracts on the expression of caspase-3 level in HepG2 cells. HepG2 cells were treated with 30 μg/mL samples for 6 h before being exposed to t-BHP (700 μmol/L) for 3 h. (A) The expressions of pro-caspase-3, cleaved caspase-3 and β-actin were used for normalization and verification of protein loading; (B) Quantitative pro-caspase-3 and cleaved caspase-3 expression after normalization to β-actin. (a) Control; (b) 700 μmol/L t-BHP treated; (c) 30 μg/mL PEF + 700 μmol/L t-BHP; (d) 30 μg/mL DMF + 700 μmol/L t-BHP; (e) 30 μg/mL EAF + 700 μmol/L t-BHP; (f) 30 μg/mL BAF + 700 μmol/L t-BHP; (g) 30 μg/mL RF + 700 μmol/L t-BHP. Different letters above bars indicate significant difference (by ANOVA, p < 0.05). Result are expressed as mean ± SD (n ≥ 3). + , treated; −, untreated.