Inhibitory effect of echinocystic acid on 12-O-tetradecanoylphorbol-13-acetate-induced dermatitis in mice

被引:21
作者
Joh, Eun-Ha [1 ]
Jeong, Jin-Ju [2 ,3 ]
Kim, Dong-Hyun [2 ,3 ]
机构
[1] Korea Atom Energy Res Inst, Dept Res Reactor Utilizat, Radioisotope Res Div, Taejon 305353, South Korea
[2] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, Seoul 130701, South Korea
[3] Kyung Hee Univ, Dept Pharm, Seoul 130701, South Korea
关键词
Codonopsis lanceolata; Campanulaceae; Echinocystic acid; Lancemaside A; Acute dermatitis; NF-KAPPA-B; INDUCED MOUSE DERMATITIS; INFLAMMATION; IDENTIFICATION; ACTIVATION; SAPONINS; DISEASE; BINDING;
D O I
10.1007/s12272-013-0092-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The rhizome of Codonopsis lanceolata (family Campanulaceae), which contains lancemaside A as a main constituent, is frequently used in the traditional Chinese medicine for the treatment of inflammatory diseases. Lancemaside A exhibits anti-inflammatory effect in vitro and in vivo. However, orally administered lancemaside A is metabolized to echinocystic acid by the intestinal microflora and the metabolite is absorbed into the blood. Therefore, to understand whether echinocystic acid is effective against skin inflammatory diseases, we assessed its inhibitory effect against 12-O-tetra decanoylphorbol-13-acetate (TPA)-induced ear inflammation in mice. Topically administered echinocystic acid potently suppressed TPA-induced ear swelling. The suppression rates at 0.05 and 0.10 % concentrations were 65 and 73 %, respectively. Echinocystic acid also inhibited TPA-induced myeloperoxidase activity, as well as COX-2, iNOS, TNF-alpha and IL-1 beta expressions. Echinocystic acid inhibited NF-kappa B in TPA-treated mouse ears, as well as in lipopolysaccharide-stimulated peritoneal macrophages. Its potency is comparable with that of dexamethasone. These findings indicate that echinocystic acid may ameliorate inflammatory diseases, such as dermatitis.
引用
收藏
页码:225 / 231
页数:7
相关论文
共 25 条
[1]   IMMUNOSUPPRESSION BY GLUCOCORTICOIDS - INHIBITION OF NF-KAPPA-B ACTIVITY THROUGH INDUCTION OF I-KAPPA-B SYNTHESIS [J].
AUPHAN, N ;
DIDONATO, JA ;
ROSETTE, C ;
HELMBERG, A ;
KARIN, M .
SCIENCE, 1995, 270 (5234) :286-290
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   Cyclooxygenase enzymes in allergic inflammation and asthma [J].
Carey, MA ;
Germolec, DR ;
Langenbach, R ;
Zeldin, DC .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2003, 69 (2-3) :157-162
[4]   Protein kinase Cα-mediated chemotaxis of neutrophils requires NF-κB activity but is independent of TNFα signaling in mouse skin in vivo [J].
Cataisson, C ;
Pearson, AJ ;
Torgerson, S ;
Nedospasov, SA ;
Yuspa, SH .
JOURNAL OF IMMUNOLOGY, 2005, 174 (03) :1686-1692
[5]   TOPICALLY APPLIED STEROIDS IN CORNEAL DISEASE .1. ROLE OF INFLAMMATION IN STROMAL ABSORPTION OF DEXAMETHASONE [J].
COX, WV ;
LEIBOWITZ, HM ;
KUPFERMAN, A .
ARCHIVES OF OPHTHALMOLOGY, 1972, 88 (03) :308-+
[6]   Anti-inflammatory and analgesic activity of Baccharis trimera: Identification of its active constituents [J].
Gene, RM ;
Cartana, C ;
Adzet, T ;
Mann, E ;
Parella, T ;
Canigueral, S .
PLANTA MEDICA, 1996, 62 (03) :232-235
[7]   MACROPHAGE CYTOTOXICITY - ROLE FOR L-ARGININE DEIMINASE AND IMINO-NITROGEN OXIDATION TO NITRITE [J].
HIBBS, JB ;
TAINTOR, RR ;
VAVRIN, Z .
SCIENCE, 1987, 235 (4787) :473-476
[8]   Dihydrolipoic acid inhibits skin tumor promotion through anti-inflammation and anti-oxidation [J].
Ho, Yuan-Soon ;
Lai, Ching-Shu ;
Liu, Hsin-I ;
Ho, Sheng-Yow ;
Tai, Chein ;
Pan, Min-Hsiung ;
Wang, Ying-Jan .
BIOCHEMICAL PHARMACOLOGY, 2007, 73 (11) :1786-1795
[9]   Rapid identification of triterpenoid saponins in the roots of Codonopsis lanceolata by liquid chromatography-mass spectrometry [J].
Ichikawa, Makoto ;
Ohta, Sanae ;
Komoto, Noriko ;
Ushijima, Mitsuyasu ;
Kodera, Yukihiro ;
Hayama, Minoru ;
Shirota, Osamu ;
Sekita, Setsuko ;
Kuroyanagi, Masanori .
JOURNAL OF NATURAL MEDICINES, 2008, 62 (04) :423-429
[10]   Echinocystic acid ameliorates lung inflammation in mice and alveolar macrophages by inhibiting the binding of LPS to TLR4 in NF-κB and MAPK pathways [J].
Joh, Eun-Ha ;
Gu, Wan ;
Kim, Dong-Hyun .
BIOCHEMICAL PHARMACOLOGY, 2012, 84 (03) :331-340