Stanley P L, Steiner S, Havens M, Tramposch K M
Bristol-Myers Squibb Pharmaceutical Research Institute, Buffalo, N.Y.
Skin Pharmacol. 1991;4(4):262-71. doi: 10.1159/000210960.
It is well known that applications of a single dose of 12-O-tetradecanoylphorbol-13-acetate (TPA) to mouse ears induces an acute inflammatory reaction consisting of erythema, edema and polymorphonuclear leukocyte (PMN) infiltration. We report here that multiple topical applications of TPA to mouse ears produce a prolonged inflammatory reaction characterized by increases in ear weight, inflammatory cell infiltration and epidermal hyperplasia. TPA was applied 5 times over 10 days to mouse ears. Epidermal thickness and PMN infiltration (myeloperoxidase content) increased 3- and 160-fold, respectively, by day 3 and remained elevated over control values throughout the test period. Ear weight was elevated from day 1 and remained high. Hydrocortisone 17-valerate and betamethasone dipropionate significantly reduced all three parameters of inflammation. Indomethacin and two other cyclo-oxygenase inhibitors, and an antihistamine had little or no effect on any of the parameters. This chronic skin inflammation model may be more relevant for evaluating anti-inflammatory compounds than the acute TPA model because the test compounds are applied after the inflammatory lesion is established, which mirrors the use of clinical anti-inflammatory drugs. Also this model may be more selective than the acute TPA model for compounds which affect leukotriene production since other pharmacological agents which are active in the acute model are not active in the multiple-application model.
众所周知,给小鼠耳部单次涂抹12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)会引发急性炎症反应,包括红斑、水肿和多形核白细胞(PMN)浸润。我们在此报告,对小鼠耳部多次局部涂抹TPA会产生持续时间较长的炎症反应,其特征为耳部重量增加、炎症细胞浸润和表皮增生。在10天内对小鼠耳部涂抹TPA 5次。到第3天,表皮厚度和PMN浸润(髓过氧化物酶含量)分别增加了3倍和160倍,并且在整个测试期间均高于对照值。耳部重量从第1天开始升高并持续保持较高水平。17 - 戊酸氢化可的松和二丙酸倍他米松显著降低了所有三个炎症参数。吲哚美辛和其他两种环氧化酶抑制剂以及一种抗组胺药对任何参数几乎没有影响。这种慢性皮肤炎症模型可能比急性TPA模型更适用于评估抗炎化合物,因为测试化合物是在炎症病变形成后应用的,这反映了临床抗炎药物的使用情况。此外,对于影响白三烯产生的化合物,该模型可能比急性TPA模型更具选择性,因为在急性模型中具有活性的其他药理剂在多次涂抹模型中无活性。