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Cytoprotective Effects of Sulfuretin from Rhus verniciflua through Regulating of Heme Oxygenase-1 in Human Dental Pulp Cells  

Lee, Dong-Sung (Hanbang Body Fluid Research Center, Wonkwang University)
Kim, Kyoung-Su (Standardized Material Bank for New Botanical Drugs, College of Pharmacy, Wonkwang University)
Ko, Wonmin (Standardized Material Bank for New Botanical Drugs, College of Pharmacy, Wonkwang University)
Keo, Samell (Standardized Material Bank for New Botanical Drugs, College of Pharmacy, Wonkwang University)
Jeong, Gil-Saeng (College of Pharmacy, Wonkwang University)
Oh, Hyuncheol (Hanbang Body Fluid Research Center, Wonkwang University)
Kim, Youn-Chul (Hanbang Body Fluid Research Center, Wonkwang University)
Publication Information
Natural Product Sciences / v.19, no.1, 2013 , pp. 54-60 More about this Journal
Abstract
Rhus verniciflua Stokes (Anacadiaceae) is a plant that is native to East Asian countries, such as Korea, China, and Japan, and it has been found to exert various biological activities including antioxidative, anti-aggregatory, anti-inflammatory, anti-mutagenic, and apoptotic effects. Sulfuretin is one of the major flavonoid component isolated from the heartwood of R. verniciflua. Reactive oxygen species (ROS), produced via dental adhesive bleaching agents and pulpal disease, can cause oxidative stress. In the present study, we isolated sulfuretin from R. verniciflua and demonstrated that sulfuretin possesses cytoprotective effects against hydrogen peroxide ($H_2O_2$)-induced dental cell death. $H_2O_2$ is a representative ROS and causes cell death through necrosis in human dental pulp (HDP) cells. $H_2O_2$-induced cytotoxicity and production of ROS were blocked in the presence of sulfuretin, and these effects were dose dependent. Sulfuretin also increased heme oxygenase-1 (HO-1) protein expression. In addition, to determine whether sulfuretin-induced HO-1 expression mediated this cytoprotective effect, HDP cells were cotreated with sulfuretin in the absence or presence of SnPP, an inhibitor of HO activity. Sulfuretin-dependent HO-1 expression was required for suppression of $H_2O_2$-induced HDP cell death and ROS generation. These results indicate that sulfuretin-dependent HO-1 expression was required for the inhibition of $H_2O_2$-induced cell death and ROS generation. In addition, sulfuretin may be used to prevent functional dental cell death and thus may be useful as a pulpal disease agent.
Keywords
Rhus verniciflua; Sulfuretin; Human dental pulp cells; Heme oxygenase-1; Cytoprotective effect;
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