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抗过敏药物对人中性粒细胞的作用位点。

Action sites of antiallergic drugs on human neutrophils.

作者信息

Taniguchi K, Masuda Y, Takanaka K

机构信息

Department of Toxicology, Niigata College of Pharmacy, Japan.

出版信息

Jpn J Pharmacol. 1990 Jan;52(1):101-8. doi: 10.1254/jjp.52.101.

Abstract

Sites of the inhibitory action of antiallergic drugs (azelastine, oxatomide, tranilast, repirinast and amlexanox) on human neutrophils were investigated by measuring leukotriene B4 formation, arachidonic acid release and superoxide generation. Results obtained in this study were as follows: (i) Formations of leukotriene B4 by neutrophils activated with a calcium ionophore (A23187) were effectively inhibited by all types of antiallergic drugs examined here, although the required concentrations were within a range of 20-200 microM. (ii) Releases of arachidonic acid from activated cells were diminished by azelastine and oxatomide that were classified as basic antiallergic drugs. On the contrary, acidic antiallergic agents including repirinast, amlexanox and tranilast enhanced the arachidonic acid liberation. (iii) Generations of superoxide from neutrophils activated with either phorbol 12-myristate 13-acetate or n-formyl-methionyl-leucyl-phenylalanine were effectively diminished only by the basic antiallergic drugs.

摘要

通过测量白三烯B4的生成、花生四烯酸的释放和超氧化物的产生,研究了抗组胺药(氮卓斯汀、奥沙米特、曲尼司特、瑞吡司特和氨来呫诺)对人中性粒细胞的抑制作用位点。本研究获得的结果如下:(i)尽管所需浓度在20-200 microM范围内,但所有类型的抗组胺药均有效抑制了用钙离子载体(A23187)激活的中性粒细胞生成白三烯B4。(ii)被归类为碱性抗组胺药的氮卓斯汀和奥沙米特减少了活化细胞中花生四烯酸的释放。相反,包括瑞吡司特、氨来呫诺和曲尼司特在内的酸性抗组胺药增强了花生四烯酸的释放。(iii)仅碱性抗组胺药有效减少了用佛波醇12-肉豆蔻酸酯13-乙酸酯或N-甲酰甲硫氨酰亮氨酰苯丙氨酸激活的中性粒细胞产生的超氧化物。

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