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. 2022 Apr 12;13:876550. doi: 10.3389/fphar.2022.876550

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Copyright © 2022 Jiang, Zhang, Zheng, Sun and Ding.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Que reduced lipid ROS and lipid droplet accumulation in steatotic L-02 cells (n = 3). (A) The effect of Que treatment on L-02 cell viability. (B) Representative fluorescence intensity images of cellular lipid ROS by BODIPY 581/591 C11 obtained by flow cytometry. (C) Flow cytometric analysis of fluorescence intensity. (D) Oil Red O staining of L-02 cells (scale bar = 50 μm). (E) TG content in L-02 cells. The data are expressed as the mean ± SD from three independent experiments. **, p < 0.01 and *, p < 0.05.