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Purpose
The formulated ethanol extract (DA-9601) of
Artemisia asiatica
has pronounced anti-inflammatory activities and exhibits cytoprotective effects against gastrointestinal damage. Here we investigated whether eupatilin, a major component of DA-9601, has a property of antioxidant activity and protects gastric epithelial cells from H
2
O
2
-induced damage.
Methods
The protective effect of eupatilin against H
2
O
2
-induced damages was studied in gastric epithelial AGS cells by measuring wound healing, cell proliferation, and cell viability. Global gene expression profiling was obtained by high-density microarray.
Results
Hydrogen peroxide significantly delayed epithelial migration in wounded area. In contrast, eupatilin prevented the reduction of epithelial migration induced by H
2
O
2
. Eupatilin also ameliorated H
2
O
2
-induced actin disruption in AGS cells. Interestingly, treatment with eupatilin dramatically inhibited FeSO
4
-induced ROS production in a dose-dependent manner. In addition, eupatilin protected cells from FeSO
4
-induced F-actin disruption. With high-density microarray, we identified dozens of genes whose expressions were up-regulated in H
2
O
2
-treated cells. We found that eupatilin reduces the expression of such oxidative-responsible genes as HO-1, PLAUR and TNFRSF10A in H
2
O
2
-treated cells.
Conclusion
These results suggest that eupatilin acts as a novel antioxidant and may play an important role in DA-9601-mediated effective repair of the gastric mucosa.