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AWD 12 - 281,一种高度选择性的磷酸二酯酶4抑制剂,在过敏性皮炎模型中对炎症反应的预防和治疗有效。

AWD 12-281, a highly selective phosphodiesterase 4 inhibitor, is effective in the prevention and treatment of inflammatory reactions in a model of allergic dermatitis.

作者信息

Bäumer Wolfgang, Gorr Gilbert, Hoppmann Joachim, Ehinger Andreas M, Rundfeldt Chris, Kietzmann Manfred

机构信息

Department of Pharmacology, Toxicology and Pharmacy, School of Veterinary Medicine, Buenteweg 17, D-30559 Hannover, Germany.

出版信息

J Pharm Pharmacol. 2003 Aug;55(8):1107-14. doi: 10.1211/0022357021585.

Abstract

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.

摘要

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。

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