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Ethylacetate extract from Draconis Resina inhibits LPS-induced inflammatory responses in vascular smooth muscle cells and macrophages via suppression of ROS production
被引:26
|作者:
Heo, Sook-Kyoung
Yi, Hyo-Seung
Yun, Hyun-Jeong
Ko, Chang-Hyun
Choi, Jae-Woo
Park, Sun-Dong
[1
]
机构:
[1] Univ Dongguk, Cardiovasc Med Res Ctr, Gyeongju City 780714, Gyeongbuk, South Korea
关键词:
Draconis Resina;
Anti-inflammation;
Anti-atherosclerosis agent;
ROS;
Human aortic smooth muscle cells;
TOLL-LIKE RECEPTORS;
DRAGONS BLOOD;
TOLL-LIKE-RECEPTOR-4;
EXPRESSION;
CROTON URUCURANA;
NITRIC-OXIDE;
DISEASE;
PROLIFERATION;
MONOCYTES;
ENDOTOXIN;
D O I:
10.1016/j.fct.2009.06.043
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
Draconis Resina (DR) is a type of dragon's blood resin obtained from Daemomorops draco BL. (Palmae). DR has long been used as a traditional Korean herbal medicine, and is currently used in traditional clinics to treat wounds, tumors, diarrhea, and rheumatism, insect bites and other conditions. In this study, we evaluated fractionated extracts of DR to determine if they inhibited the production of interleukin-1 beta (IL-1 beta) and the expression of cyclooxygenase (COX)-2. The results of this analysis revealed that the ethylacetate extract of Draconis Resina (DREA) was more potent than that of other extracts. Moreover, DREA inhibited the production of nitric oxide (NO), reactive oxygen species (ROS), prostaglandin E-2 (PGE(2)), tumor necrosis factor-alpha (TNF-alpha), IL-8 and IL-6 in lipopolysaccharide (LPS)-treated human aortic smooth muscle cells (HASMC) and RAW 264.7 macrophages. Furthermore, treatment with an NADPH oxidase assembly inhibitor, AEBSF, efficiently blocked LPS-induced mitogen-activated protein kinases (MAPKs) activation, as did DREA. These findings indicate that DREA inhibits the production of NO, PGE(2), TNF-alpha, IL-8, and IL-6 by LPS via the inhibition of ROS production, which demonstrates that DREA inhibits LPS-induced inflammatory responses via the suppression of ROS production. Taken together, these results indicate that DREA has the potential for use as an anti-atherosclerosis agent. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:1129 / 1136
页数:8
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