Gilman S C, Carlson R P, Chang J, Lewis A J
Agents Actions. 1985 Oct;17(1):53-9. doi: 10.1007/BF01966682.
The antiinflammatory activity of the immunomodulatory agent Wy-18,251 (3-(p-chlorophenyl)thiazolo-[3,2-a]benzimidazole-2-acetic acid) was examined using a variety of antiinflammatory, analgesic and antipyretic animal models in comparison to aspirin, levamisole and indomethacin. The acute antiinflammatory and analgesic activity of Wy-18,251 (ED50 = 100-200 mg/kg, p.o.) was similar to aspirin, but in contrast to aspirin Wy-18,251 failed to demonstrate antipyretic activity. Wy-18,251 (10-100 mg/kg, p.o.) also inhibited chronic inflammatory responses in the adjuvant- and collagen-induced arthritis models. Wy-18,251 was a modest inhibitor of prostaglandin biosynthesis but did not inhibit either 5- or 15-lipoxygenase enzymes. Wy-18,251 (up to 480 mg/kg, p.o.) produced little gastrointestinal pathology in 16 h fasted rats. The combined immunomodulatory and antiinflammatory activity of Wy-18,251 suggests that this agent may have therapeutic promise in certain immunoinflammatory diseases including rheumatoid arthritis.
使用多种抗炎、镇痛和解热动物模型,将免疫调节剂Wy-18,251(3-(对氯苯基)噻唑并-[3,2-a]苯并咪唑-2-乙酸)的抗炎活性与阿司匹林、左旋咪唑和吲哚美辛进行了比较。Wy-18,251的急性抗炎和镇痛活性(口服半数有效量ED50 = 100 - 200 mg/kg)与阿司匹林相似,但与阿司匹林不同的是,Wy-18,251未表现出解热活性。Wy-18,251(口服剂量10 - 100 mg/kg)在佐剂性关节炎和胶原诱导性关节炎模型中也能抑制慢性炎症反应。Wy-18,251是前列腺素生物合成的适度抑制剂,但不抑制5-脂氧合酶或15-脂氧合酶。在禁食16小时的大鼠中,Wy-18,251(口服剂量高达480 mg/kg)几乎不产生胃肠道病变。Wy-18,251的免疫调节和抗炎活性相结合表明,该药物在包括类风湿性关节炎在内的某些免疫炎症性疾病中可能具有治疗前景。