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巨噬细胞产生前列腺素及抗炎药物的作用。

Prostaglandin production by macrophages and the effect of anti-inflammatory drugs.

作者信息

Bray M A, Gordon D

出版信息

Br J Pharmacol. 1978 Aug;63(4):635-42. doi: 10.1111/j.1476-5381.1978.tb17276.x.

Abstract

1 Macrophages derived from peritoneal cavity inflammatory exudates of guinea-pigs produced substantial amounts of prostaglandin E2-like activity during in vitro culture, so providing the basis for an experimental model of prostaglandin production during inflammatory reactions. 2 Dose-related inhibition of prostaglandin biosynthesis was demonstrated by 16 acidic non-steroidal anti-inflammatory drugs. 3 Seven anti-inflammatory glucocorticosteroid preparations inhibited prostaglandin production in a dose-related manner. The relative potencies of dexamethasone, prednisolone and hydrocortisone were consistent with clinical anti-inflammatory ranking. Cortisone, however, failed to inhibit macrophage prostaglandin production. 4 Three other agents used in the treatment of inflammatory joint diseases were examined. Sodium aurothiomalate inhibited prostaglandin production, although higher concentrations were toxic to macrophages. D-Penicillamine did not affect macrophage prostaglandin production. Colchicine, in contrast, enhanced prostaglandin production at some concentrations. 5 The probable significance of macrophages as a source of prostaglandins, during inflammatory responses, is discussed.

摘要
  1. 从豚鼠腹腔炎性渗出物中提取的巨噬细胞在体外培养期间产生了大量类似前列腺素E2的活性物质,从而为炎症反应期间前列腺素产生的实验模型提供了基础。2. 16种酸性非甾体抗炎药表现出与剂量相关的前列腺素生物合成抑制作用。3. 7种抗炎糖皮质激素制剂以剂量相关的方式抑制前列腺素的产生。地塞米松、泼尼松龙和氢化可的松的相对效力与临床抗炎排名一致。然而,可的松未能抑制巨噬细胞前列腺素的产生。4. 对用于治疗炎性关节疾病的其他三种药物进行了检测。金硫代苹果酸钠抑制前列腺素的产生,尽管较高浓度对巨噬细胞有毒性。D-青霉胺不影响巨噬细胞前列腺素的产生。相比之下,秋水仙碱在某些浓度下会增强前列腺素的产生。5. 讨论了巨噬细胞作为炎症反应期间前列腺素来源的可能意义。

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