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人离体支气管和肺实质条对SRS-A及其他哮喘性支气管痉挛介质的反应。

Response of human isolated bronchial and lung parenchymal strips to SRS-A and other mediators of asthmatic bronchospasm.

作者信息

Ghelani A M, Holroyde M C, Sheard P

出版信息

Br J Pharmacol. 1980;71(1):107-12. doi: 10.1111/j.1476-5381.1980.tb10915.x.

DOI:10.1111/j.1476-5381.1980.tb10915.x
PMID:7470732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2044407/
Abstract

1 The responses of human isolated bronchial and lung parenchymal strips to cumulative doses of slow reacting substance of anaphylaxis (SRS-A), histamine, prostaglandin F2 alpha (PGF2 alpha) and acetylcholine have been examined, after storing the tissues overnight in Krebs solution at 4 degrees C. 2 Both tissues contracted to all four agonists. The order of potency (as determined by height of maximal contraction) was: bronchial strip: acetylcholine greater than histamine = PGF2 alpha greater than SRS-A, and parenchymal strip: PGF2 alpha much greater than histamine = SRS-A greater than acetylcholine. 3 Maximal contractions to SRS-A of both the human bronchial and parenchymal strips were approx. 30% of the maximal contractions produced by the most potent agonist on each tissue (PGF2 alpha on the parenchymal strip and acetylcholine on the bronchial strip). SRS-A, therefore, does not have a powerful direct contractile effect on either parenchymal or bronchial strip of human lung, and is approximately equipotent on both tissues. A part of the broncho-constrictor activity of SRS-A in vivo may be mediated via indirect pathways. 4 The selective SRS-A antagonist, FPL 55712, was approximately equipotent in antagonizing contractions induced by SRS-A on both human bronchial and parenchymal strips.

摘要
  1. 将人体离体支气管和肺实质条带在4℃的 Krebs 溶液中过夜保存后,检测其对累积剂量的过敏反应慢反应物质(SRS - A)、组胺、前列腺素 F2α(PGF2α)和乙酰胆碱的反应。2. 两种组织对所有四种激动剂均产生收缩反应。效价顺序(由最大收缩高度确定)为:支气管条带:乙酰胆碱>组胺 = PGF2α>SRS - A,肺实质条带:PGF2α>>组胺 = SRS - A>乙酰胆碱。3. 人体支气管和肺实质条带对 SRS - A 的最大收缩约为每种组织上最有效激动剂(肺实质条带上的 PGF2α和支气管条带上的乙酰胆碱)产生的最大收缩的30%。因此,SRS - A 对人肺的实质或支气管条带均没有强大的直接收缩作用,且在两种组织上的效力大致相当。SRS - A 在体内的部分支气管收缩活性可能通过间接途径介导。4. 选择性 SRS - A 拮抗剂 FPL 55712 在拮抗 SRS - A 诱导的人体支气管和肺实质条带收缩方面效力大致相当。

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Response of human isolated bronchial and lung parenchymal strips to SRS-A and other mediators of asthmatic bronchospasm.人离体支气管和肺实质条对SRS-A及其他哮喘性支气管痉挛介质的反应。
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