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依布硒啉抑制豚鼠肺实质条带的收缩反应。

Ebselen inhibits contractile responses of guinea-pig parenchymal lung strips.

作者信息

Leurs R, Bast A, Timmerman H

机构信息

Department of Pharmacochemistry, Faculty of Chemistry, Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

Eur J Pharmacol. 1990 Apr 10;179(1-2):193-9. doi: 10.1016/0014-2999(90)90418-6.

Abstract

Ebselen is a new anti-inflammatory drug with a wide spectrum of pharmacological activities. Since this compound might be useful in diseases related to airway inflammation we evaluated the effects of ebselen on the contractile responses of guinea-pig parenchymal lung strip. Ebselen and its sulfur analogue RP 62373 depressed both histamine H1-receptor-mediated and KCl-induced (50 mM) contractions of guinea-pig lung strips equipotently. The responses to histamine were only affected via depression of the maximal response; treatment with 3 microM ebselen for 30 min resulted in depression to 77 +/- 5% of the control value, whereas 10 and 30 microM inhibited the contractions to 53 +/- 4 and 52 +/- 4% of the control value respectively. The responses after membrane depolarisation (50 mM KCl) were less sensitive to ebselen pretreatment; 10 microM ebselen inhibited contractions by only 20%, whereas 30 and 100 microM depressed the response by approximately 50%. These observations were evaluated in the context of the activities of ebselen already described. The effects of lipoxygenase, cyclooxygenase, protein kinase C inhibition and thiol alkylation were studied, using established agents. However, although interaction with critical thiol groups might explain our data, the mode of action of ebselen is yet not fully elucidated.

摘要

依布硒啉是一种具有广泛药理活性的新型抗炎药物。由于该化合物可能对与气道炎症相关的疾病有用,我们评估了依布硒啉对豚鼠肺实质条收缩反应的影响。依布硒啉及其硫类似物RP 62373同等程度地抑制组胺H1受体介导的和氯化钾诱导的(50 mM)豚鼠肺条收缩。对组胺的反应仅通过最大反应的降低而受到影响;用3 microM依布硒啉处理30分钟导致反应降低至对照值的77±5%,而10 microM和30 microM分别将收缩抑制至对照值的53±4%和52±4%。膜去极化(50 mM氯化钾)后的反应对依布硒啉预处理不太敏感;10 microM依布硒啉仅抑制收缩20%,而30 microM和100 microM使反应降低约50%。这些观察结果在已描述的依布硒啉活性背景下进行了评估。使用已确立的药物研究了脂氧合酶、环氧化酶、蛋白激酶C抑制和硫醇烷基化的作用。然而,尽管与关键硫醇基团的相互作用可能解释我们的数据,但依布硒啉的作用方式尚未完全阐明。

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