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Inhibition of Skin Inflammation and Atopic Dermatitis by Topical Application of a Novel Ceramide Derivative, K112PC-5, in Mice
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  • Inhibition of Skin Inflammation and Atopic Dermatitis by Topical Application of a Novel Ceramide Derivative, K112PC-5, in Mice
  • Inhibition of Skin Inflammation and Atopic Dermatitis by Topical Application of a Novel Ceramide Derivative, K112PC-5, in Mice
저자명
Kang. Jong-Soon,Lee. Chang-Woo,Lee. Ki-Ho,Han. Mi-Hwa,Lee. Hyun-Ju,Youm. Jong-Kyung,Jeong. Se-Kyoo,Park. Byeong-Deog,Han. Sang-B
간행물명
Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea
권/호정보
2008년|31권 8호|pp.1004-1009 (6 pages)
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

PC-9S (N-Ethanol-2-mirystyl-3-oxo-stearamide) is a synthetic ceramide and has been known to be effective in atopic and psoriatic patients. K112PC-5 (2-Acetyl-N-(1,3-dihydroxyisopropyl)-tetradecanamide) is a novel ceramide derivative of PC-9S. In the present study, we examined the effect of K112PC-5 on macrophage and T lymphocyte function in primary macrophages and splenocytes, respectively, as well as the effect of topical application of K112PC-5 on skin inflammation and atopic dermatitis (AD) in mouse models. K112PC-5 inhibited lipopolysaccharide-induced nitrite generation in mouse peritoneal macrophages in a dose-dependent manner. However, K112PC-5 did not affect concanavalin A-induced proliferation, interleukin (IL)-2 secretion and IL-4 secretion in mouse splenocytes. In addition, K112PC-5 significantly suppressed the increase in phorbol ester-induced ear thickness in BALB/c mice. Further study demonstrated that topical application of K112PC-5 also inhibited AD induced by extracts of dust mites, Dermatophagoides pteronyssinus and Dermatophagoides farinae, in NC/Nga mice. Taken together, these results showed that K112PC-5 exerted an anti-inflammatory effect both in vitro and in vivo and proved to be beneficial in an animal model of AD. Our results suggest that K112PC-5 might be beneficial as a topical agent for the treatment of AD.