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血小板活化因子诱导大鼠眼部炎症及其被血小板活化因子拮抗剂L-652,731抑制的研究。

A study of PAF-induced ocular inflammation in the rat and its inhibition by the PAF antagonist, L-652,731.

作者信息

Gautheron P D, Coulbault L, Sugrue M F

机构信息

Centre de Recherche, Merck Sharp & Dohme-Chibret, Riom-Cedex, France.

出版信息

J Pharm Pharmacol. 1987 Oct;39(10):857-9. doi: 10.1111/j.2042-7158.1987.tb05135.x.

Abstract

A significant inflammatory reaction in the rat conjunctiva followed the subconjunctival injection of synthetic platelet activating factor (PAF) in doses which ranged from 10 ng to 1 microgram, an inflammatory response being evaluated as the increase in both tissue weight and extravasation of Evans blue dye in the conjunctival tissue. Inflammation was still present 6 h after the injection of 0.1 microgram of PAF. Orally administered indomethacin or BW 755C failed to alter the response to 0.1 microgram of PAF. In contrast, the PAF-induced inflammation was blocked by the oral administration of the PAF receptor antagonist, L-652,731, a dose as low as 5 mg kg-1 eliciting a significant inhibition. The topical administration of L-652,731, (two doses of 100 micrograms as a 1% suspension), elicited a slight, but significant blockade of 23%. Its antagonistic action was more striking when it was co-injected subconjunctivally with 0.1 microgram of PAF, a dose as low as 3 micrograms evoking a significant blockade. The topical administration of 0.1 microgram of PAF did not elicit a significant inflammatory reaction and this contrasts with the results obtained after its subconjunctival injection.

摘要

在大鼠结膜下注射剂量范围为10纳克至1微克的合成血小板活化因子(PAF)后,结膜出现显著的炎症反应,炎症反应通过结膜组织的组织重量增加和伊文思蓝染料外渗来评估。注射0.1微克PAF后6小时炎症仍然存在。口服吲哚美辛或BW 755C未能改变对0.1微克PAF的反应。相比之下,口服PAF受体拮抗剂L-652,731可阻断PAF诱导的炎症,低至5毫克/千克的剂量即可产生显著抑制作用。局部应用L-652,731(两剂100微克,制成1%混悬液)可产生轻微但显著的23%的阻断作用。当它与0.1微克PAF结膜下联合注射时,其拮抗作用更显著,低至3微克的剂量即可产生显著阻断作用。局部应用0.1微克PAF未引起显著的炎症反应,这与结膜下注射后的结果形成对比。

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