Topical application of a novel ceramide derivative, K6PC-9, inhibits dust mite extract-induced atopic dermatitis-like skin lesions in NC/Nga mice

被引:17
作者
Kang, Jong Soon [1 ]
Youm, Jong-Kyung [2 ,3 ]
Jeong, Se Kyoo [2 ,3 ]
Park, Byeong Deog [2 ]
Yoon, Won Kee [1 ]
Han, Mi Hwa [1 ]
Lee, Hyunju [1 ]
Han, Sang-Bae [4 ]
Lee, Kiho [1 ]
Park, Song-Kyu [1 ]
Lee, Seung Hun [5 ]
Yang, Kyu-Hwan [6 ]
Moon, Eun-Yi [7 ]
Kim, Hwan Mook [1 ]
机构
[1] Korea Res Inst Biosci & Biotechnol, Bioevaluat Ctr, Cheongwon, Chungbuk, South Korea
[2] Yonsei Univ, Brain Korea 21 Project Med Sci, Seoul 120749, South Korea
[3] Neopharm Co Ltd, Taejon, South Korea
[4] Chungbuk Natl Univ, Coll Pharm, Cheongju, Chungbuk, South Korea
[5] Yonsei Univ, Coll Med, Dept Dermatol, Seoul, South Korea
[6] Kyungwon Univ, Gachon Bionano Res Inst, Kyunggido, South Korea
[7] Sejong Univ, Dept Biosci & Biotechnol, Seoul, South Korea
关键词
K6PC-9; skin inflammation; atopic dermatitis; TNF-alpha; adhesion molecule;
D O I
10.1016/j.intimp.2007.08.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Atopic dermatitis (AD) is a chronic inflammatory skin disease. K6PC-9 (N-Ethanol-2-hexyl-3-oxo-decanamide) is a novel synthetic ceramide derivative of PC-9S (N-Ethanol-2-mirystyl-3-oxo-stearamide), which was known to be effective in atopic and psoriatic patients. To investigate the immunomodulatory activity of K6PC-9, we examined the effect of K6PC-9 on T lymphocyte and macrophage function and the effect of topical application of K6PC-9 on skin inflammation and AD-like skin lesions in mouse models. K6PC-9 had no effect on concanavalin A-induced proliferation, interleukin (IL)-2 secretion and IL-4 secretion in mouse splenocytes. In contrast, lipopolysaccharide-induced nitrite generation was potently suppressed by K6PC-9 in mouse peritoneal macrophages. In mouse model of skin inflammation, K6PC-9 inhibited phorbol ester-induced increase in ear thickness and expression of tumor necrosis factor-alpha in the ear of BALB/c mice. Topical application of K6PC-9 also suppressed mite extract-induced AD-like skin lesions in NC/Nga mice. Increase in ear thickness was significantly inhibited by K6PC-9 in this model. K6PC-9 also blocked the infiltration of mast cells and neutrophils into the ear. Further study demonstrated that the mRNA expression of tumor necrosis factor-a and adhesion molecules, such as vascular cell adhesion molecule-1, intercellular adhesion molecule-1, E-selectin, was also suppressed by K6PC-9 in the ear of mite extract-treated NC/Nga mice. Taken together, the results presented in this report show that K6PC-9 has an anti-inflammatory potential and exerts beneficial effects in an animal model of AD, indicating that K6PC-9 might be used as a topical agent for the treatment of AD. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1589 / 1597
页数:9
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