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本文引用的文献

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J Pharmacol Methods. 1981 Aug;6(1):1-4. doi: 10.1016/0160-5402(81)90077-2.
2
The inhibition by hydrocortisone of prostaglandin biosynthesis in rat peritoneal leucocytes is correlated with intracellular macrocortin levels.氢化可的松对大鼠腹膜白细胞中前列腺素生物合成的抑制作用与细胞内巨皮质素水平相关。
Br J Pharmacol. 1981 Oct;74(2):322-4. doi: 10.1111/j.1476-5381.1981.tb09974.x.
3
A new method for inducing fatal, IgE-mediated, bronchial and cardiovascular anaphylaxis in the rat.一种在大鼠中诱导致命性、IgE 介导的支气管和心血管过敏反应的新方法。
J Pharmacol Methods. 1983 May;9(3):175-81. doi: 10.1016/0160-5402(83)90036-0.
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Immune responses in rats sensitized with aerosolized antigen. Antibody formation, lymphoblastic responses and mast cell and mucous cell development related to bronchial reactivity.经雾化抗原致敏的大鼠的免疫反应。抗体形成、淋巴细胞反应以及与支气管反应性相关的肥大细胞和黏液细胞发育。
Int Arch Allergy Appl Immunol. 1983;72(1):71-8. doi: 10.1159/000234843.
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Differences in biological activation of arachidonic acid in perfused lungs from guinea pig, rat and man.豚鼠、大鼠和人灌注肺中花生四烯酸生物活化的差异。
Eur J Pharmacol. 1980 Mar 7;62(1):89-96. doi: 10.1016/0014-2999(80)90484-7.
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Bronchial anaphylaxis in actively sensitized Sprague Dawley rats: studies on mediators involved.主动致敏的斯普拉格-道利大鼠的支气管过敏反应:关于相关介质的研究
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7
Characterization of various antiallergic agents using a new method for inducing systemic anaphylaxis in the rat.使用一种诱导大鼠全身性过敏反应的新方法对各种抗过敏药物进行表征。
J Pharmacol Methods. 1984 Jun;11(3):219-26. doi: 10.1016/0160-5402(84)90040-8.
8
Responses to leukotriene C4 in the perfused rat lung.灌注大鼠肺脏对白三烯C4的反应。
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Respiratory responses to leukotrienes and biogenic amines in normal and hyperreactive rats.
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10
Ketotifen: current views on its mechanism of action and their therapeutic implications.酮替芬:关于其作用机制及其治疗意义的当前观点。
Respiration. 1984;45(4):411-21. doi: 10.1159/000194648.

泼尼松龙和酮替芬对大鼠离体肺中抗原诱导的支气管收缩和介质释放的影响。

The effect of prednisolone and ketotifen on the antigen-induced bronchoconstriction and mediator release in rat isolated lungs.

作者信息

Ottenhof M, Ufkes J G, Van Rooij H H

出版信息

Br J Pharmacol. 1985 Nov;86(3):627-36. doi: 10.1111/j.1476-5381.1985.tb08939.x.

DOI:10.1111/j.1476-5381.1985.tb08939.x
PMID:4063584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1916715/
Abstract

Using a new method for inducing IgE-mediated, systemic anaphylaxis in the rat both prednisolone and ketotifen had been shown previously to be effective in suppressing the bronchial anaphylaxis in vivo. In order to study the mode of action underlying their bronchoprotective effect, both agents were also tested on the antigen-induced bronchoconstriction in rat isolated lungs in relation to the mediator release in the lung-effluent. The presence of histamine, 5-hydroxytryptamine (5-HT) and SRS-A could be detected biologically in the lung-effluent during bronchoconstriction. Histamine and 5-HT were determined quantitatively by means of h.p.l.c. with fluorimetric detection, whereas SRS-A was determined using the guinea-pig ileum in a cascade set-up. Although both prednisolone and ketotifen inhibited the antigen-induced bronchoconstriction effectively, it appeared that only prednisolone suppressed the release of histamine, 5-HT and SRS-A in the lung-effluent significantly, whereas ketotifen had no effect. On account of these data it is suggested that the bronchoprotective effect of prednisolone is mainly based on inhibition of the release of the mediators involved, whereas the effect of ketotifen may be based on receptor antagonism.

摘要

采用一种在大鼠中诱导IgE介导的全身性过敏反应的新方法,先前已证明泼尼松龙和酮替芬在体内抑制支气管过敏反应方面均有效。为了研究它们支气管保护作用的潜在作用方式,还在大鼠离体肺中测试了这两种药物对抗原诱导的支气管收缩的作用,并与肺灌洗液中的介质释放相关联。在支气管收缩期间,可以从肺灌洗液中生物学检测到组胺、5-羟色胺(5-HT)和慢反应物质A(SRS-A)的存在。组胺和5-HT通过高效液相色谱荧光检测法定量测定,而SRS-A则使用级联装置中的豚鼠回肠进行测定。虽然泼尼松龙和酮替芬均有效抑制抗原诱导的支气管收缩,但似乎只有泼尼松龙能显著抑制肺灌洗液中组胺、5-HT和SRS-A的释放,而酮替芬则无作用。基于这些数据,提示泼尼松龙的支气管保护作用主要基于抑制相关介质的释放,而酮替芬的作用可能基于受体拮抗作用。