Newsholme S J, Schwartz L
Department of Toxicology SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406.
Inflammation. 1993 Feb;17(1):25-31. doi: 10.1007/BF00916389.
The effect of rolipram, an isozyme IV-selective inhibitor of cAMP-specific phosphodiesterase, was evaluated in a guinea pig eye model of tissue eosinophilia. (R)-rolipram was administered by gavage to guinea pigs 1 h prior to topical ocular challenge with a mixture of leukotrienes (LTs) (10 ng LTB4 + 1000 ng LTD4/eye) or with histamine dihydrochloride (1 mg/eye). Conjunctivae were evaluated histologically 6 h after challenge. Eosinophil counts per millimeter of conjunctival epithelium in LT-challenged animals that received (R)-rolipram at dosages of 0.1, 0.3, 1, 3, or 10 mg/kg were reduced by 63, 63, 84, 81 and 90% respectively, compared to LT-challenged controls. Reduction was statistically significant (P < 0.05) at all dosages. Eosinophil counts per millimeter of epithelium in histamine-challenged animals that received 10 mg/kg (R)-rolipram were reduced by 79% compared to histamine-challenged controls (P < 0.01). The results indicate that (R)-rolipram inhibits the response to two distinct classes of mediator in this model of eosinophil infiltration, adding support to the contention that isozyme IV-selective cAMP phosphodiesterase inhibitors offer therapeutic potential for human asthma.
在豚鼠组织嗜酸性粒细胞增多症的眼部模型中,评估了环磷腺苷特异性磷酸二酯酶同工酶IV选择性抑制剂咯利普兰的作用。在用白三烯(LTs)混合物(10 ng LTB4 + 1000 ng LTD4/眼)或盐酸组胺(1 mg/眼)进行局部眼部激发前1小时,通过灌胃给豚鼠施用(R)-咯利普兰。激发后6小时对结膜进行组织学评估。与LT激发的对照组相比,接受0.1、0.3、1、3或10 mg/kg剂量(R)-咯利普兰的LT激发动物每毫米结膜上皮中的嗜酸性粒细胞计数分别减少了63%、63%、84%、81%和90%。所有剂量下的减少均具有统计学意义(P < 0.05)。与组胺激发的对照组相比,接受10 mg/kg(R)-咯利普兰的组胺激发动物每毫米上皮中的嗜酸性粒细胞计数减少了79%(P < 0.01)。结果表明,在这个嗜酸性粒细胞浸润模型中,(R)-咯利普兰抑制了对两种不同类型介质的反应,这支持了同工酶IV选择性环磷腺苷磷酸二酯酶抑制剂对人类哮喘具有治疗潜力的观点。