
doi: 10.1042/cs0670153
Background: Feldberg & Kellaway [1] were the first to demonstrate the formation and release from envenomed dog and monkey lungs of a substance which caused a delayed and slow contraction of the guinea-pig jejunum; subsequently, Kellaway & Trethewie [2] described release of a slow-reacting substance (SRS) during acute anaphylaxis of the guinea-pig lung. Brocklehurst [3, 4] later reported the formation of an SRS, which he called slow-reacting substance of anaphylaxis (SRS-A), during anaphylaxis of guinea-pig, rabbit, monkey and human lungs. This substance had similar activity to SRS on guinea-pig ileum and was unaffected by the newly developed antihistamine, mepyramine. Release of SRS-A was demonstrated during antigen-induced constriction of bronchioles from subjects with asthma [5], suggesting that SRS-A might be of importance in the pathogenesis of human asthma [6, 7]. The development of techniques for the generation and partial purification of SRS-A from the rat peritoneal cavity [6] and intact guinea-pig lungs [8] permitted characterization of its biological properties.
Lung Diseases, Guinea Pigs, Bronchi, In Vitro Techniques, Cardiovascular System, Leukotriene B4, Mice, Dogs, Cricetinae, Animals, Humans, Anaphylaxis, Lung, Leukotriene E4, Chemotaxis, Hemodynamics, Haplorhini, Asthma, Rats, Respiratory Function Tests, Mucus, Cattle, SRS-A, Rabbits
Lung Diseases, Guinea Pigs, Bronchi, In Vitro Techniques, Cardiovascular System, Leukotriene B4, Mice, Dogs, Cricetinae, Animals, Humans, Anaphylaxis, Lung, Leukotriene E4, Chemotaxis, Hemodynamics, Haplorhini, Asthma, Rats, Respiratory Function Tests, Mucus, Cattle, SRS-A, Rabbits
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