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大鼠腹腔中白三烯生物合成的抑制作用。

Inhibition of leukotriene biosynthesis in the rat peritoneal cavity.

作者信息

Young P R, Bell R L, Lanni C, Summers J B, Brooks D W, Carter G W

机构信息

Immunosciences Research Area, Abbott Laboratories, Abbott Park, IL 60064.

出版信息

Eur J Pharmacol. 1991 Dec 3;205(3):259-66. doi: 10.1016/0014-2999(91)90907-8.

Abstract

In the search for a model of leukotriene (LT) production to provide a method to determine in vivo 5-lipoxygenase (5-LO) inhibitory activity by various compounds, a passive anaphylactic reaction in the rat peritoneal cavity was examined, refined and characterized. The reaction, produced by passive sensitization with an i.p. injection of rabbit anti-bovine serum albumin (anti-BSA) followed by an i.p. injection of BSA, resulted in the biosynthesis of large amounts of sulfidopeptide LTs measurable by immunoassay or by reversed phase high performance liquid chromatography. The oral activity of several 5-LO inhibitors has been examined using this model. An example of these is zileuton (Abbott-64077), a potent 5-lipoxygenase inhibitor now under clinical evaluation. Zileuton inhibited sulfidopeptide LT biosynthesis in the rat peritoneal cavity in a dose-dependent manner (ED50 = 3 mg/kg). WY-49,232, MK-866, BW A4C and phenidone also produced good activity with ED50 values of 6, 8, 11 and 17 mg/kg, respectively. This modified rat peritoneal anaphylaxis model appears to be a valuable tool for establishing in vivo activity of 5-LO inhibitors.

摘要

为寻找一种白三烯(LT)生成模型,以提供一种测定各种化合物体内5-脂氧合酶(5-LO)抑制活性的方法,对大鼠腹腔内的被动过敏反应进行了研究、改进和特性分析。该反应是通过腹腔注射兔抗牛血清白蛋白(抗BSA)进行被动致敏,随后腹腔注射BSA产生的,导致大量可通过免疫测定或反相高效液相色谱法测量的硫肽白三烯的生物合成。使用该模型检测了几种5-LO抑制剂的口服活性。其中一个例子是齐留通(雅培-64077),一种目前正在进行临床评估的强效5-脂氧合酶抑制剂。齐留通以剂量依赖的方式抑制大鼠腹腔内硫肽白三烯的生物合成(半数有效剂量[ED50]=3mg/kg)。WY-49,232、MK-866、BW A4C和非那宗也表现出良好的活性,其ED50值分别为6、8、11和17mg/kg。这种改良的大鼠腹腔过敏模型似乎是确定5-LO抑制剂体内活性的一种有价值的工具。

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