Abstract |
Aloperine has been shown to inhibit 2,4-dinitrofluorobenzene ( DNFB) induced allergic contact dermatitis in BALB/c mice. In the present study, we further investigated the effect of aloperine on DNFB-induced atopic dermatitis-like skin lesions in NC/Nga mice. NC/Nga mice elicited atopic dermatitis-like skin lesions after the topical application of DNFB. Aloperine treatment significantly inhibited dermatitis index and ear thickness in DNFB-treated NC/Nga mice in a dose-dependent manner. Eosinophils, mast cells infiltration into the ears and plasma level of immunoglobulin (Ig) E were also suppressed by aloperine treatment. Finally, cytokine ( interleukin (IL)-1β, IL-4, IL-6, IL-10, IL-13, tumor necrosis factor (TNF)-α and interferon (IFN)-γ) productions in ear biopsies homogenates were significantly elevated after DNFB challenge. Topical application of aloperine increased the immunosuppressive cytokine IL-10 level, while it reduced other cytokines production in a dose-dependent manner. Taken together, these data suggest that aloperine may be one of the effective therapeutic agents for the treatment of atopic dermatitis.
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Authors | Xiao-Ying Yuan, Hui-Min Ma, Rui-Zhi Li, Rui-Yan Wang, Wei Liu, Jian-You Guo |
Journal | European journal of pharmacology
(Eur J Pharmacol)
Vol. 658
Issue 2-3
Pg. 263-9
(May 11 2011)
ISSN: 1879-0712 [Electronic] Netherlands |
PMID | 21371468
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 Elsevier B.V. All rights reserved. |
Chemical References |
- Piperidines
- Quinolizidines
- Interleukin-10
- Immunoglobulin E
- aloperine
- Dinitrofluorobenzene
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Topics |
- Administration, Topical
- Animals
- Dermatitis, Atopic
(chemically induced, drug therapy, immunology, metabolism)
- Dinitrofluorobenzene
(pharmacology)
- Down-Regulation
(drug effects)
- Ear
(pathology)
- Female
- Immunoglobulin E
(blood)
- Interleukin-10
(metabolism)
- Mast Cells
(drug effects, immunology)
- Mice
- Piperidines
(administration & dosage, pharmacology, therapeutic use)
- Quinolizidines
- Th1 Cells
(drug effects, immunology)
- Th2 Cells
(drug effects, immunology)
- Up-Regulation
(drug effects)
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