Suppr超能文献

环氧化酶产物在白三烯A4、B4、C4、D4和E4肺部作用中的角色。

Role of cyclooxygenase products in the lung action of leukotrienes A4, B4, C4, D4 and E4.

作者信息

Sirois P, Chagnon M, Borgeat P, Vallerand P

出版信息

Pharmacology. 1985;31(4):225-36. doi: 10.1159/000138119.

Abstract

Leukotrienes (LT) LTA4, LTB4, LTC4, LTD4 and LTE4 induced marked contractions of guinea pig lung parenchymal strips mounted in organ baths. These contractions were inhibited differentially (40-50% for LTA4, LTC4, LTD4 and LTE4, and 90% for LTB4) by indomethacin (20 micrograms.ml-1; 55.9 microM). Two novel inhibitors of thromboxane synthetase (OKY-1581 and OKY-046) reduced the myotropic activity of the lung strips and the release of prostaglandins and thromboxanes from the perfused guinea pig lungs stimulated by LTB4 and LTD4. The release of cyclooxygenase products prostaglandin F2 alpha, thromboxane B2 and 12-hydroxyheptadecatrienoic acid by guinea pig lungs following stimulation with LTB4 and LTD4 was also measured by gas chromatography-mass spectrometry. The role of prostaglandins and thromboxanes in the lung actions of leukotrienes was confirmed using a cascade superfusion system and classical organ baths. Although prostaglandins and thromboxanes contribute to the contractile effect of LTB4 on the guinea pig lung whereas they may play a lesser role in the action of the peptidoleukotrienes (approx. 40-50%), stimulation of their release by the peptidoleukotrienes is many times more effective than by LTB4.

摘要

白三烯(LT)LTA4、LTB4、LTC4、LTD4和LTE4可使置于器官浴槽中的豚鼠肺实质条产生明显收缩。吲哚美辛(20微克·毫升-1;55.9微摩尔)可不同程度地抑制这些收缩(LTA4、LTC4、LTD4和LTE4的抑制率为40%-50%,LTB4的抑制率为90%)。两种新型血栓素合成酶抑制剂(OKY-1581和OKY-046)可降低肺条的肌收缩活性以及LTB4和LTD4刺激的灌注豚鼠肺中前列腺素和血栓素的释放。还用气相色谱-质谱法测定了LTB4和LTD4刺激后豚鼠肺中环氧合酶产物前列腺素F2α、血栓素B2和12-羟基十七碳三烯酸的释放。使用级联超灌注系统和经典器官浴槽证实了前列腺素和血栓素在白三烯肺作用中的作用。虽然前列腺素和血栓素有助于LTB4对豚鼠肺的收缩作用,而它们在肽白三烯的作用中可能起较小作用(约40%-50%),但肽白三烯刺激它们释放的效果比LTB4高许多倍。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验