Bäumer Wolfgang, Gorr Gilbert, Hoppmann Joachim, Ehinger Andreas M, Rundfeldt Chris, Kietzmann Manfred
Department of Pharmacology, Toxicology and Pharmacy, School of Veterinary Medicine, Buenteweg 17, D-30559 Hannover, Germany.
J Pharm Pharmacol. 2003 Aug;55(8):1107-14. doi: 10.1211/0022357021585.
AWD 12-281 (N-(3,5-dichloro-4-pyridinyl)-2-[1-(4-fluorobenzyl)-5-hydroxy-1H-indol-3-yl]-2-oxoacetamide), a phosphodiesterase 4 inhibitor, which is optimized for topical administration, was tested in a model of allergic dermatitis in mice. To obtain an allergic dermatitis, BALB/c mice were sensitized to toluene-2,4-diisocyanate (TDI). The allergic reaction was challenged by topical administration of TDI onto the mice ears. AWD 12-281 was tested for its anti-inflammatory potential by oral, intraperitoneal and topical administration. The phosphodiesterase 4 inhibitor, cilomilast (SB 207499), and/or the corticosteroid, diflorasone diacetate, were used as reference compounds. Given orally and intraperitoneally 2 h before as well as 5 and 24 h after TDI challenge, AWD 12-281 showed no, or only a transient inhibition of the allergen-induced ear swelling, whereas cilomilast significantly inhibited this ear swelling. Applied topically onto the ears before TDI challenge, AWD 12-281, cilomilast and diflorasone diacetate caused total inhibition of ear swelling 24 h after challenge, confirmed by a decrease of the pro-inflammatory cytokines interleukin-4, interleukin-6 and macrophage inhibitory protein-2. Administered topically after TDI challenge as therapeutic intervention, AWD 12-281 and diflorasone diacetate caused significant inhibition of ear swelling; cilomilast failed to do so. These results indicate that topically administered AWD 12-281 may be potent in the prevention and treatment of allergic/inflammatory skin diseases.
AWD 12 - 281(N -(3,5 - 二氯 - 4 - 吡啶基)- 2 - [1 -(4 - 氟苄基)- 5 - 羟基 - 1H - 吲哚 - 3 - 基] - 2 - 氧代乙酰胺),一种经优化用于局部给药的磷酸二酯酶4抑制剂,在小鼠过敏性皮炎模型中进行了测试。为诱导过敏性皮炎,将BALB/c小鼠用甲苯 - 2,4 - 二异氰酸酯(TDI)致敏。通过将TDI局部施用于小鼠耳部来激发过敏反应。通过口服、腹腔注射和局部给药测试了AWD 12 - 281的抗炎潜力。磷酸二酯酶4抑制剂西洛司特(SB 207499)和/或皮质类固醇二氟拉松双醋酸酯用作参考化合物。在TDI激发前2小时以及激发后5小时和24小时口服和腹腔注射AWD 12 - 281,对变应原诱导的耳部肿胀未显示出抑制作用,或仅显示出短暂抑制,而西洛司特显著抑制了这种耳部肿胀。在TDI激发前局部应用于耳部,AWD 12 - 281、西洛司特和二氟拉松双醋酸酯在激发后24小时导致耳部肿胀完全受到抑制,促炎细胞因子白细胞介素 - 4、白细胞介素 - 6和巨噬细胞抑制蛋白 - 2的减少证实了这一点。在TDI激发后作为治疗干预局部给药,AWD 12 - 281和二氟拉松双醋酸酯显著抑制了耳部肿胀;西洛司特未能做到这一点。这些结果表明,局部给药的AWD 12 - 281在预防和治疗过敏性/炎症性皮肤病方面可能具有效力。