PMID- 16914137 OWN - NLM STAT- MEDLINE DCOM- 20070111 LR - 20131121 IS - 0014-2999 (Print) IS - 0014-2999 (Linking) VI - 546 IP - 1-3 DP - 2006 Sep 28 TI - Inhibition of scratching behavior associated with allergic dermatitis in mice by tacrolimus, but not by dexamethasone. PG - 189-96 AB - Itching is the most important problem in many allergic and inflammatory skin diseases especially in atopic dermatitis. However, animal models for allergic dermatitis useful for the study of itching have rarely been established. We established a mouse allergic dermatitis model involving frequent scratching behavior by repeated painting with 2,4-dinitrofluorobenzene (DNFB) acetone solution onto the mouse skin, and comparatively examined the effects of tacrolimus and dexamethasone on the dermatitis and associated scratching behavior. Repeated DNFB painting caused typical dermatitis accompanied by elevated serum immunoglobulin E (IgE) and frequent scratching behavior. An apparent thickening of the epidermis and dermis, and the significant accumulation of inflammatory cells were observed. Increased interferon (IFN)-gamma mRNA expression and the induction of interleukin (IL)-4 and IL-5 mRNA expression were also observed in the skin lesion. The scratching behavior was inhibited by dibucaine and naloxone. Although tacrolimus reduced the increased expression of IFN-gamma and IL-4 mRNA, dexamethasone potently depressed that of IFN-gamma, IL-4 and IL-5 mRNA. Dexamethasone inhibited the accumulation of lymphocytes and eosinophils, although tacrolimus did not. Both drugs failed to inhibit the elevation of serum IgE levels. Tacrolimus significantly inhibited the scratching behavior that was associated with the inhibition of nerve fiber extension into the epidermis, whereas dexamethasone failed to have any effect. The mouse dermatitis model seems to be beneficial for the study of itching associated with allergic dermatitis, such as atopic dermatitis, and tacrolimus seems to exhibit an anti-itch effect through the inhibition of nerve fiber extension at least in part. FAU - Inagaki, Naoki AU - Inagaki N AD - Department of Pharmacology, Gifu Pharmaceutical University, 5-6-1 Mitahorahigashi, Gifu 502-8585, Japan. inagakin@gifu-pu.ac.jp FAU - Shiraishi, Noriko AU - Shiraishi N FAU - Igeta, Katsuhiro AU - Igeta K FAU - Itoh, Tomokazu AU - Itoh T FAU - Chikumoto, Takao AU - Chikumoto T FAU - Nagao, Masafumi AU - Nagao M FAU - Kim, John Fan AU - Kim JF FAU - Nagai, Hiroichi AU - Nagai H LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20060725 PL - Netherlands TA - Eur J Pharmacol JT - European journal of pharmacology JID - 1254354 RN - 0 (Allergens) RN - 0 (Anesthetics, Local) RN - 0 (Antipruritics) RN - 0 (Glucocorticoids) RN - 0 (Interleukin-5) RN - 0 (Narcotic Antagonists) RN - 0 (RNA, Messenger) RN - 207137-56-2 (Interleukin-4) RN - 36B82AMQ7N (Naloxone) RN - 37341-29-0 (Immunoglobulin E) RN - 7S5I7G3JQL (Dexamethasone) RN - 82115-62-6 (Interferon-gamma) RN - D241E059U6 (Dinitrofluorobenzene) RN - L6JW2TJG99 (Dibucaine) RN - WM0HAQ4WNM (Tacrolimus) SB - IM MH - Allergens/immunology MH - Anesthetics, Local/pharmacology MH - Animals MH - Antipruritics/*pharmacology/therapeutic use MH - Behavior, Animal/*drug effects MH - Dermatitis, Allergic Contact/*drug therapy/immunology/pathology MH - Dermatitis, Atopic/*drug therapy/immunology/pathology MH - Dexamethasone/pharmacology MH - Dibucaine/pharmacology MH - Dinitrofluorobenzene/immunology MH - Disease Models, Animal MH - Glucocorticoids/pharmacology MH - Immunoglobulin E/blood MH - Interferon-gamma/biosynthesis MH - Interleukin-4/biosynthesis MH - Interleukin-5/metabolism MH - Male MH - Mice MH - Mice, Inbred BALB C MH - Naloxone/pharmacology MH - Narcotic Antagonists/pharmacology MH - Pruritus/*prevention & control MH - RNA, Messenger/biosynthesis MH - Skin/drug effects/immunology/pathology MH - Tacrolimus/*pharmacology/therapeutic use EDAT- 2006/08/18 09:00 MHDA- 2007/01/12 09:00 CRDT- 2006/08/18 09:00 PHST- 2006/04/17 00:00 [received] PHST- 2006/07/02 00:00 [revised] PHST- 2006/07/13 00:00 [accepted] PHST- 2006/08/18 09:00 [pubmed] PHST- 2007/01/12 09:00 [medline] PHST- 2006/08/18 09:00 [entrez] AID - S0014-2999(06)00760-6 [pii] AID - 10.1016/j.ejphar.2006.07.019 [doi] PST - ppublish SO - Eur J Pharmacol. 2006 Sep 28;546(1-3):189-96. doi: 10.1016/j.ejphar.2006.07.019. Epub 2006 Jul 25.