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2
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本文引用的文献

1
The release of histamine and formation of a slow-reacting substance (SRS-A) during anaphylactic shock.过敏性休克期间组胺的释放及慢反应物质(SRS-A)的形成。
J Physiol. 1960 Jun;151(3):416-35. doi: 10.1113/jphysiol.1960.sp006449.
2
Some quantitative uses of drug antagonists.药物拮抗剂的一些定量应用。
Br J Pharmacol Chemother. 1959 Mar;14(1):48-58. doi: 10.1111/j.1476-5381.1959.tb00928.x.
3
Mechanics of respiration in unanesthetized guinea pigs.未麻醉豚鼠的呼吸力学
Am J Physiol. 1958 Feb;192(2):364-8. doi: 10.1152/ajplegacy.1958.192.2.364.
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Occurrence of an unidentified substance during anaphylactic shock in cavy lung.豚鼠肺部过敏性休克期间出现不明物质。
J Physiol. 1953 Apr 28;120(1-2):16P-17P.
5
Slow reacting substances of anaphylaxis: identification of leukotrienes C-1 and D from human and rat sources.过敏反应迟缓反应物质:从人和大鼠来源中鉴定白三烯C-1和D
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3710-4. doi: 10.1073/pnas.77.6.3710.
6
Effects of intravenous administration of slow-reacting substance of anaphylaxis, histamine, bradykinin, and prostaglandin F2alpha on pulmonary mechanics in the guinea pig.静脉注射过敏反应慢反应物质、组胺、缓激肽和前列腺素F2α对豚鼠肺力学的影响。
J Clin Invest. 1974 Jun;53(6):1679-85. doi: 10.1172/JCI107719.
7
Selective inhibitor of slow reacting substance of anaphylaxis.过敏反应迟缓反应物质的选择性抑制剂。
Nat New Biol. 1973 Oct 17;245(146):215-7. doi: 10.1038/newbio245215a0.
8
Pulmonary response to antigen infusion in the sensitized guinea pig: modification by atropine.致敏豚鼠肺部对抗原注入的反应:阿托品的影响
J Appl Physiol. 1975 Dec;39(6):916-9. doi: 10.1152/jappl.1975.39.6.916.
9
Lung mechanics following antigen challenge of Ascaris suum-sensitive rhesus monkeys.猪蛔虫敏感恒河猴抗原激发后的肺力学
J Appl Physiol. 1976 Nov;41(5 Pt. 1):668-76. doi: 10.1152/jappl.1976.41.5.668.
10
Differential effects of a partially purified preparation of slow-reacting substance of anaphylaxis on guinea pig tracheal spirals and parenchymal strips.过敏反应慢反应物质的部分纯化制剂对豚鼠气管螺旋条和实质条的不同作用。
J Clin Invest. 1979 Jan;63(1):1-5. doi: 10.1172/JCI109262.

白三烯C-1和D在体内和体外的气道与血管活性比较

Comparative airway and vascular activities of leukotrienes C-1 and D in vivo and in vitro.

作者信息

Drazen J M, Austen K F, Lewis R A, Clark D A, Goto G, Marfat A, Corey E J

出版信息

Proc Natl Acad Sci U S A. 1980 Jul;77(7):4354-8. doi: 10.1073/pnas.77.7.4354.

DOI:10.1073/pnas.77.7.4354
PMID:6933488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC349833/
Abstract

The pharmacologic activities of leukotrienes C-1 and D(LTC-1 and LTD), constituents of slow reacting substance of anaphylaxis (SRS-A), were evaluated in vitro on airway contractile tissues and in vivo on pulmonary mechanical function, mean systemic arterial pressure, and cutaneous microcirculation. In vitro both LTC-1 and LTD were potent and selective peripheral airway agonists, being more active than histamine; furthermore, LTD was active on peripheral airways at concentrations 1/100th those of LTC-1. The concentration-effect relationship for LTD and the profile of antagonism by FPL 55712 are consistent with the activity of this molecule at two separate peripheral airway receptors. In vivo, LTC-1 and LTD were nearly equally active in their effects on pulmonary mechanics, and the pattern of alterations was consistent with the predominant site of action being in the lung periphery. Furthermore, both agents had a direct systemic arterial hypotensive effect and were vasoactive on the cutaneous microcirculation. Thus, these compounds are likely to be major mediators of the pathologic alterations in immediate type hypersensitivity reactions in which peripheral airway constriction and hypotension are prominent features.

摘要

对过敏反应慢反应物质(SRS-A)的成分白三烯C-1和D(LTC-1和LTD)的药理活性进行了体外气道收缩组织评估以及体内肺机械功能、平均体动脉压和皮肤微循环评估。在体外,LTC-1和LTD都是强效且选择性的外周气道激动剂,比组胺更具活性;此外,LTD在外周气道上的活性浓度是LTC-1的1/100。LTD的浓度-效应关系以及FPL 55712的拮抗作用特征与该分子在两个不同外周气道受体上的活性一致。在体内,LTC-1和LTD对肺机械功能的影响几乎同样活跃,且改变模式与主要作用部位在肺外周一致。此外,两种药物都有直接的体动脉降压作用,并且对皮肤微循环有血管活性作用。因此,这些化合物可能是速发型超敏反应中病理改变的主要介质,其中外周气道收缩和低血压是突出特征。