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花生四烯酸脂氧合酶抑制剂BW755C对组织损伤的抑制作用。

Inhibition of tissue damage by the arachidonate lipoxygenase inhibitor BW755C.

作者信息

Higgs G A, Mugridge K G, Moncada S, Vane J R

出版信息

Proc Natl Acad Sci U S A. 1984 May;81(9):2890-2. doi: 10.1073/pnas.81.9.2890.

Abstract

The effects of three anti-inflammatory drugs, which interfere with arachidonic acid transformation by three different enzymes, have been compared by using a simple model of tissue damage and foreign body rejection. In groups of control rats, subcutaneously implanted polyester sponges were rejected after a mean of 12 days. Indomethacin, which selectively inhibits prostaglandin synthesis, did not significantly change time to rejection but BW755C (3-amino-1-[m-(trifluoromethyl) phenyl]-2-pyrazoline), which is a dual inhibitor of prostaglandin and leukotriene synthesis, prolonged time to rejection to a mean of 22 days. The anti-inflammatory steroid dexamethasone, which reduces arachidonic acid metabolism by stimulating the formation of a phospholipase inhibitor, prolonged time to sponge rejection as BW755C did. Treatment with BW755C or dexamethasone was also accompanied by a reduction in total leukocyte numbers in inflammatory exudates collected at 1-14 days, whereas indomethacin increased leukocyte migration on days 1 and 2 and had no effect at later times. These results suggest that the inhibition of the leukotriene-forming lipoxygenase suppresses leukocyte activation and that this leads to a reduced rate of tissue damage in experimental inflammation.

摘要

通过使用组织损伤和异物排斥的简单模型,比较了三种抗炎药物的效果,这三种药物通过三种不同的酶干扰花生四烯酸的转化。在对照组大鼠中,皮下植入的聚酯海绵平均在12天后被排斥。选择性抑制前列腺素合成的吲哚美辛并没有显著改变排斥时间,但BW755C(3-氨基-1-[间-(三氟甲基)苯基]-2-吡唑啉),一种前列腺素和白三烯合成的双重抑制剂,将排斥时间延长至平均22天。抗炎类固醇地塞米松通过刺激磷脂酶抑制剂的形成来减少花生四烯酸代谢,与BW755C一样延长了海绵排斥时间。用BW755C或地塞米松治疗还伴随着在1 - 14天收集的炎性渗出物中白细胞总数的减少,而吲哚美辛在第1天和第2天增加了白细胞迁移,在后期没有影响。这些结果表明,对白三烯形成的脂氧合酶的抑制抑制了白细胞的激活,并且这导致实验性炎症中组织损伤的速率降低。

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