Inhibition of inflammations and macrophage activation by ginsenoside-Re isolated from Korean ginseng (Panax ginseng C.A. Meyer)

被引:73
作者
Paul, Souren
Shin, Heung Sop [2 ]
Kang, Sun Chul [1 ]
机构
[1] Daegu Univ, Dept Biotechnol, Coll Engn, Kyongsan 712714, Kyoungbook, South Korea
[2] Korea Polytech Univ, Dept Chem Engn & Biotechnol, Shihung 429793, Gyeonggido, South Korea
关键词
Anti-inflammatory activity; Saponins; BALB/c mice; Cytokines; Raw; 264.7; macrophage; ANTIINFLAMMATORY ACTIVITY; NITRIC-OXIDE; PROINFLAMMATORY CYTOKINES; OXIDATIVE STRESS; TUMOR PROMOTION; MURINE SKIN; MOUSE PAW; IN-VIVO; SAPONINS; ACID;
D O I
10.1016/j.fct.2012.02.035
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
This study was undertaken to evaluate the effect of ginsenoside-Re (Gin-Re) isolated from roots of Panax ginseng on carrageenan-induced paw and TPA-induced skin inflammations in experimental mice. Moreover, to confirm further the anti-inflammatory activities of Gin-Re, LPS-induced macrophage activation model was also used. Exposure of TPA on the ear of BALB/c mice caused a marked increase in both ear thickness and skin water content. Gin-Re caused significant decrease in ear thickness and subsequently reduced the water content compared to only TPA treated group (p<0.05). Furthermore, histological analysis clearly confirmed that Gin-Re inhibited the inflammatory responses of skin inflammation in animal model. Gin-Re was responded well in inhibiting paw thickness, MDA level and also NO level in carrageenan induced paw edema model compared to only carrageenan treated group. Treatment with Gin-Re inhibited secretion levels of inflammatory mediators such as tumor necrosis factor alpha (TNF alpha), and interleukin-1 beta (IL-1 beta) in LPS-stimulated murine macrophage Raw 264.7 cells. Despite the fact that Gin-Re has weaker anti-inflammatory potential than the positive controls, indomethacin and hydrocortisone, in the entire group tested, quite effective anti-inflammatory activity was shown by Gin-Re, which could be helpful to develop medicinal preparations for various inflammatory diseases. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1354 / 1361
页数:8
相关论文
共 41 条
[1]
In vivo and in vitro antiinflammatory activity of saikosaponins [J].
Benito, PB ;
Martínez, MJA ;
Sen, AMS ;
Gómez, AS ;
Matellano, LF ;
Contreras, SS ;
Lanza, AMD .
LIFE SCIENCES, 1998, 63 (13) :1147-1156
[2]
Progressive iron overload enhances chemically mediated tumor promotion in murine skin [J].
Bhasin, G ;
Kausar, H ;
Alam, MS ;
Athar, M .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2003, 409 (02) :262-273
[3]
MODULATION OF MOUSE EAR EDEMA BY CYCLOOXYGENASE AND LIPOXYGENASE INHIBITORS AND OTHER PHARMACOLOGICAL AGENTS [J].
CARLSON, RP ;
ONEILLDAVIS, L ;
CHANG, J ;
LEWIS, AJ .
AGENTS AND ACTIONS, 1985, 17 (02) :197-204
[4]
CHANG HY, 2009, EVID-BASED COMPL ALT, DOI DOI 10.1093/ECAM/NEP027
[5]
Difference in absorption of the two structurally similar flavonoid glycosides, hyperoside and isoquercitrin, in rats [J].
Chang, Q ;
Zuo, Z ;
Chow, MSS ;
Ho, WKK .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 59 (03) :549-555
[6]
Antinociceptive and Antiinflammatory effects of niga-ichigoside F1 and 23-hydroxytormentic acid obtained from Rubus coreanus [J].
Choi, J ;
Lee, KT ;
Ha, J ;
Yun, SY ;
Ko, CD ;
Jung, HJ ;
Park, HJ .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2003, 26 (10) :1436-1441
[7]
COREGULATION OF COLLAGENASE AND COLLAGENASE INHIBITOR PRODUCTION BY PHORBOL-MYRISTATE ACETATE IN HUMAN-SKIN FIBROBLASTS [J].
CLARK, SD ;
WILHELM, SM ;
STRICKLIN, GP ;
WELGUS, HG .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1985, 241 (01) :36-44
[8]
de Oliveira ACC, 2001, COMP BIOCHEM PHYS C, V130, P369, DOI 10.1016/S1532-0456(01)00262-9
[9]
Proinflammatory cytokines [J].
Dinarello, CA .
CHEST, 2000, 118 (02) :503-508
[10]
Garcia-Pastor P, 1999, J PHARMACOL EXP THER, V289, P166