Apoptosis Induction by the Total Flavonoids from <i>Arachniodes exilis</i> in HepG2 Cells through Reactive Oxygen Species-Mediated Mitochondrial Dysfunction Involving MAPK Activation

<table>The effect of TFAE on cell proliferation inhibition in HepG2 and LO2 cells for 24 or 48 h by CCK-8 assay. <svg height="17.825001" id="M10" style="vertical-align:-3.13504pt" version="1.1" viewbox="0 0 69.150002 17.825001" width="69.150002" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
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</svg>, TFAE-treated group compared with the negative control group. <svg height="19.65" id="M11" style="vertical-align:-3.13504pt" version="1.1" viewbox="0 0 70.224998 19.65" width="70.224998" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
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</svg>, the inhibition ratio of TFAE-treated LO2 cells group compared with TFAE-treated HepG2 cells group.</table>

Evidence-Based Complementary and Alternative Medicine

fig1

Figure 1

Figure 1: Apoptosis Induction by the Total Flavonoids from <i>Arachniodes exilis</i> in HepG2 Cells through Reactive Oxygen Species-Mediated Mitochondrial Dysfunction Involving MAPK Activation 

Figure 1 | Apoptosis Induction by the Total Flavonoids from Arachniodes exilis in HepG2 Cells through Reactive Oxygen Species-Mediated Mitochondrial Dysfunction Involving MAPK Activation 