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5-脂氧合酶抑制剂在生化和体内功能试验中的特性研究

Characterization of 5-lipoxygenase inhibitors in biochemical and functional in vivo assays.

作者信息

Smith W G, Shaffer A F, Currie J L, Thompson J M, Kim S, Rao T, Isakson P C

机构信息

Inflammatory Diseases Research, Searle Research and Development, Skokie, Illinois, USA.

出版信息

J Pharmacol Exp Ther. 1995 Dec;275(3):1332-8.

PMID:8531100
Abstract

Several potent and selective inhibitors of 5-lipoxygenase (5-LO) have been recently developed with excellent activity in certain in vivo assays of leukotriene production. The efficacy of three such inhibitors that have been in clinical trials (zileuton, A-78773 and ZD2138) were evaluated in: 1) ex vivo whole blood assay, 2) dermal Arthus reaction, and 3) functional airway response. In addition, a model of eicosanoid production in rat lung was developed that provides a simple assay for evaluation of the biochemical efficacy of 5-LO inhibitors in the lung. Bronchoalveolar lavage of rat lung with calcium ionophore A23187 resulted in rapid and robust production of PGE2, 6-keto-PGF1 alpha, thromboxane (TxB2), and leukotriene B4 (LTB4). Supplementation of lavage fluid with archidonic acid markedly augmented production of all eicosanoids except LTB4. All three inhibitors were potent and selective blockers of LTB4 production in the ex vivo whole blood assay and in the dermal Arthus reaction. In contrast, higher doses of inhibitor were needed to block LTB4 production in the rat lung lavage model than were needed to block ex vivo whole blood LTB4 production when both end points were measured in the same animal. Similarly, zileuton and A-78733 were less effective in suppressing the functional airway response to antigen in sensitized guinea pigs, whereas both inhibitors were effective in suppressing LTB4 production in the ex vivo whole blood assay. These results demonstrate that different 5-LO inhibitors have markedly distinct efficacy for inhibition of leukotriene production, depending on the animal model.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

最近已开发出几种强效且选择性的5-脂氧合酶(5-LO)抑制剂,在某些白三烯生成的体内试验中具有出色的活性。对三种已进入临床试验的此类抑制剂(齐留通、A-78773和ZD2138)的疗效进行了以下评估:1)体外全血试验;2)皮肤阿瑟斯反应;3)功能性气道反应。此外,还建立了大鼠肺中类花生酸生成模型,该模型为评估5-LO抑制剂在肺中的生化疗效提供了一种简单的试验方法。用钙离子载体A23187对大鼠肺进行支气管肺泡灌洗可快速且大量地生成前列腺素E2、6-酮-前列腺素F1α、血栓素(TxB2)和白三烯B4(LTB4)。向灌洗液中补充花生四烯酸可显著增加除LTB4外所有类花生酸的生成。在体外全血试验和皮肤阿瑟斯反应中,这三种抑制剂都是LTB4生成的强效且选择性阻断剂。相比之下,当在同一只动物中测量两个终点时,在大鼠肺灌洗模型中阻断LTB4生成所需的抑制剂剂量高于阻断体外全血LTB4生成所需的剂量。同样地,齐留通和A-78733在抑制致敏豚鼠对抗原的功能性气道反应方面效果较差,而在体外全血试验中这两种抑制剂均能有效抑制LTB4的生成。这些结果表明,不同的5-LO抑制剂对抑制白三烯生成的疗效明显不同,这取决于动物模型。(摘要截选至250字)

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