Eliakim R, Karmeli F, Okon E, Rachmilewitz D
Department of Medicine, Hadassah University Hospital, Jerusalem, Israel.
Gut. 1992 Nov;33(11):1498-503. doi: 10.1136/gut.33.11.1498.
The effects of ketotifen, a 'mast cell stabiliser,' on two models of experimental colitis were examined. The inflammatory response elicited by either trinitrobenzene sulphonic acid or acetic acid resulted in increased colonic synthesis of platelet activating factor, prostaglandin E2, thromboxane B2, leukotrienes B4 and C4, and myeloperoxidase activity. Intragastric administration of ketotifen 100 micrograms/100 grams twice daily significantly decreased mucosal damage when given prophylactically 48 hours before the induction of colitis and then throughout the experiment. This effect was consistent in both models and was accompanied by a significant reduction in mucosal generation of platelet activating factor, prostaglandin E2, thromboxane B2, and leukotrienes C4 and B4. Myeloperoxidase activity was reduced as well, reaching significance only in the acetic acid model. This study shows that both trinitrobenzene sulphonic acid and acetic acid colitis can be pharmacologically manipulated by ketotifen. The mechanism of action of ketotifen has not yet been determined. Ketotifen's potential in the treatment of active inflammatory bowel disease or in the prevention of exacertations, or both, remains to be elucidated.
研究了“肥大细胞稳定剂”酮替芬对两种实验性结肠炎模型的影响。三硝基苯磺酸或乙酸引发的炎症反应导致结肠中血小板活化因子、前列腺素E2、血栓素B2、白三烯B4和C4的合成增加,以及髓过氧化物酶活性增强。在诱导结肠炎前48小时预防性给予酮替芬100微克/100克,每日两次,然后在整个实验过程中持续给药,可显著减轻黏膜损伤。这种作用在两种模型中均一致,并伴有黏膜中血小板活化因子、前列腺素E2、血栓素B2以及白三烯C4和B4生成的显著减少。髓过氧化物酶活性也降低,仅在乙酸模型中达到显著水平。本研究表明,三硝基苯磺酸和乙酸诱导的结肠炎均可通过酮替芬进行药理调控。酮替芬的作用机制尚未确定。酮替芬在治疗活动性炎症性肠病或预防病情复发,或两者兼治方面的潜力仍有待阐明。