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抗原诱导的、从主动致敏豚鼠分离的肺实质条收缩的药理学改变

Pharmacological alteration of antigen-induced contraction of lung parenchymal strips isolated from the actively sensitized guinea pig.

作者信息

Songsiridej V, Busse W W, Buckner C K

出版信息

Eur J Pharmacol. 1983 Sep 2;92(3-4):215-22. doi: 10.1016/0014-2999(83)90289-3.

DOI:10.1016/0014-2999(83)90289-3
PMID:6138261
Abstract

Several drugs, known to influence the action or formation of histamine and SRS-A, were examined for their abilities to alter antigen (ovalbumin)-induced contractions of guinea-pig isolated lung parenchymal strips. Cumulative dose-response effects of ovalbumin were obtained on paired parenchymal strips, one used as control and the other drug treated. When used alone, mepyramine, 10(-6) M, phenoxybenzamine, 3 x 10(-5) M and FPL55712, 10(-5) M, did not alter ovalbumin-induced contractions, 5,8,11,14-eicosatetraynoic acid (ETYA), 10(-4) M, produced a small (2.5-fold) rightward shift of the dose-response curves to ovalbumin and histamine. Indomethacin, 5 x 10(-6) M, produced a small increase in the maximum response to ovalbumin and a small (2-fold) rightward shift of the histamine dose-response curve. The effect of indomethacin on ovalbumin-induced contraction was not seen in the presence of phenoxybenzamine and may therefore be due to an increase in histamine release. Combination of indomethacin with FPL55712 or ETYA did not alter antigen-induced contractions. The effect of ETYA on the histamine dose-response curve was not seen in the presence of indomethacin. Combination of phenoxybenzamine with FPL55712 or ETYA caused a marked reduction of the maximum contractile response to ovalbumin. The effect of phenoxybenzamine and ETYA was not observed in the presence of indomethacin. The results suggest that the ability of ETYA to reduce antigen responses in the absence or presence of phenoxybenzamine as well as histamine-induced contraction is related to inhibition of contractile product(s) of cyclooxygenase metabolism of arachidonic acid.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了几种已知会影响组胺和慢反应物质A(SRS - A)作用或形成的药物,考察它们改变抗原(卵清蛋白)诱导的豚鼠离体肺实质条收缩的能力。在配对的实质条上获得卵清蛋白的累积剂量 - 反应效应,一条用作对照,另一条进行药物处理。单独使用时,10⁻⁶M的甲氧苄胺、3×10⁻⁵M的酚苄明和10⁻⁵M的FPL55712不会改变卵清蛋白诱导的收缩,10⁻⁴M的5,8,11,14 - 二十碳四烯酸(ETYA)使卵清蛋白和组胺的剂量 - 反应曲线小幅(2.5倍)右移。5×10⁻⁶M的吲哚美辛使对卵清蛋白的最大反应略有增加,组胺剂量 - 反应曲线小幅(2倍)右移。在酚苄明存在的情况下未观察到吲哚美辛对卵清蛋白诱导收缩的作用,因此可能是由于组胺释放增加所致。吲哚美辛与FPL55712或ETYA联合使用不会改变抗原诱导的收缩。在吲哚美辛存在的情况下未观察到ETYA对组胺剂量 - 反应曲线的作用。酚苄明与FPL55712或ETYA联合使用导致对卵清蛋白的最大收缩反应显著降低。在吲哚美辛存在的情况下未观察到酚苄明和ETYA的作用。结果表明,在不存在或存在酚苄明的情况下ETYA降低抗原反应以及组胺诱导收缩的能力与抑制花生四烯酸环氧化酶代谢的收缩产物有关。(摘要截短于250字)

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Pharmacological alteration of antigen-induced contraction of lung parenchymal strips isolated from the actively sensitized guinea pig.抗原诱导的、从主动致敏豚鼠分离的肺实质条收缩的药理学改变
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引用本文的文献

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Histamine and leukotriene-independent guinea-pig anaphylactic shock unaccounted for by Paf-acether.组胺和白三烯非依赖性豚鼠过敏性休克不能用血小板活化因子来解释。
Br J Pharmacol. 1985 Apr;84(4):801-10. doi: 10.1111/j.1476-5381.1985.tb17374.x.
2
Blockade by methylation inhibitors of the anaphylactic response of guinea-pig lung strips.甲基化抑制剂对豚鼠肺条过敏反应的阻断作用
Br J Pharmacol. 1987 Nov;92(3):683-91. doi: 10.1111/j.1476-5381.1987.tb11372.x.