兔眼实验性角膜炎脂质介质的产生。

Journal of lipid mediators Pub Date : 1993-10-01
G W Tjebbes, J L van Delft, N J van Haeringen
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引用次数: 0

摘要

前列腺素(PG)或白三烯(LT)合成抑制剂和血小板活化因子(PAF)或LT拮抗剂在实验性角膜炎中具有抑制作用,角膜炎的临床症状可通过应用这些脂质介质重现。这表明PGE2、LTB4、LTD4和PAF参与了实验性免疫原性和中毒性角膜炎。本研究的目的是测量眼液中脂质介质的浓度及其在角膜炎期间角膜和虹膜的释放。在两种炎症模型中,房水中PGE2、LTB4、LTD4和PAF的浓度均显著高于对照组。与对照组织相比,角膜中PGE2、LTB4和LTD4的释放以及虹膜中PGE2、LTB4和PAF的释放均显著增加。结果与这些脂质介质在炎症模型中的作用一致。这些介质的合成抑制剂或拮抗剂在眼部炎症中的联合治疗使用似乎是可能的,并且可以作为局部皮质类固醇治疗的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Production of lipid mediators in experimental keratitis of rabbit eye.

The inhibitors of prostaglandin (PG) or leukotriene (LT) synthesis and antagonists of platelet-activating factor (PAF) or LTs are inhibitory in experimental keratitis and clinical symptoms of keratitis are reproduced by application of these lipid mediators. This suggests that PGE2, LTB4, LTD4, and PAF are involved in experimental immunogenic and toxic keratitis. The objective of the present study is the measurement of the concentrations of lipid mediators in the aqueous humour and their release by the cornea and iris during keratitis. In both inflammatory models the concentrations of PGE2, LTB4, LTD4, and PAF in the aqueous humour were significantly increased as compared to their controls. The release of PGE2, LTB4 and LTD4 from the cornea, and of PGE2, LTB4, and PAF from the iris was significantly increased compared to that from control tissues. The results are consistent with a role for these lipid mediators in the inflammatory models. Combined therapeutic use of synthesis inhibitors or antagonists of these mediators in eye inflammation seems possible and may serve as an alternative to topical corticosteroid therapy.

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