Suppr超能文献

环氧化酶和脂氧合酶抑制剂对恶唑酮诱导的迟发型超敏反应相关炎症的影响。

Effects of cyclooxygenase and lipoxygenase inhibitors on inflammation associated with oxazolone-induced delayed hypersensitivity.

作者信息

Meurer R, Opas E E, Humes J L

机构信息

Department of Biochemistry and Molecular Biology, Merck Sharp & Dohme Research Laboratories, Rahway, NJ 07065.

出版信息

Biochem Pharmacol. 1988 Sep 15;37(18):3511-4. doi: 10.1016/0006-2952(88)90704-6.

Abstract

Oxazolone-induced delayed hypersensitivity in mice produced swelling with concomitant increased tissue levels of leukotrienes and prostaglandins. Pharmacological agents were coapplied topically with oxazolone at the time of challenge in an attempt to modulate the immune-based inflammation. Dexamethasone inhibited both swelling and increases in eicosanoid levels. Indomethacin reduced prostaglandin levels but failed to inhibit swelling or reduce leukotriene levels. L-651,896 (2,3-dihydro-6-[3-(2-hydroxymethyl)phenyl-2-propenyl]-5-benzofuranol), a 5-lipoxygenase inhibitor, reduced leukotriene levels but did not reduce swelling or prostaglandin levels. A combination of indomethacin and L-651,896 reduced eicosanoid levels but did not reduce swelling. These data suggested that the reduction in tissue levels of 5-lipoxygenase or cyclooxygenase oxygenation products of arachidonic acid either singularly or together did not result in the concomitant reduction of the inflammation associated with oxazolone-induced delayed hypersensitivity.

摘要

恶唑酮诱导的小鼠迟发型超敏反应会产生肿胀,同时白三烯和前列腺素的组织水平升高。在激发时将药理剂与恶唑酮局部联合应用,试图调节基于免疫的炎症。地塞米松抑制了肿胀和类花生酸水平的升高。吲哚美辛降低了前列腺素水平,但未能抑制肿胀或降低白三烯水平。5-脂氧合酶抑制剂L-651,896(2,3-二氢-6-[3-(2-羟甲基)phenyl-2-丙烯基]-5-苯并呋喃醇)降低了白三烯水平,但未减轻肿胀或降低前列腺素水平。吲哚美辛和L-651,896的组合降低了类花生酸水平,但未减轻肿胀。这些数据表明,花生四烯酸的5-脂氧合酶或环氧化酶氧化产物的组织水平单独或一起降低,并不会导致与恶唑酮诱导的迟发型超敏反应相关的炎症同时减轻。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验