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KC - 404:一种对过敏反应迟缓反应物质具有拮抗作用的潜在抗过敏剂。

KC-404: a potential anti-allergic agent with antagonistic action against slow reacting substance of anaphylaxis.

作者信息

Nishino K, Ohkubo H, Ohashi M, Hara S, Kito J, Irikura T

出版信息

Jpn J Pharmacol. 1983 Apr;33(2):267-78. doi: 10.1254/jjp.33.267.

Abstract

The mode of action of a novel compound, 3-isobutyryl-2-isopropylpyrazolo [1,5-a]pyridine (KC-404), as a potential anti-allergic agent has been investigated. KC-404 was shown to have a direct bronchodilator activity in guinea pig trachea in vitro and in anesthetized guinea pig in vivo. In addition, KC-404 had a fairly selective antagonistic action against slow reacting substance of anaphylaxis (SRS-A) on guinea pig ileum in vitro. In anesthetized guinea pigs, ED50 values for intravenously and intraduodenally injected KC-404 to inhibit SRS-A-induced bronchoconstriction were 0.0014 and 0.0065 mg/kg, respectively. Much higher doses were required to inhibit bronchospasms produced by histamine or particularly by acetylcholine. Orally administered KC-404, 0.001 to 0.1 mg/kg, also showed a selective inhibitory effect on increased vascular permeability by intradermal SRS-A in guinea pigs and rats. KC-404 inhibited the immunological release of mediators, notably SRS-A from sensitized guinea pig chopped lung in vitro at 10(-8) to 10(-4) g/ml. In vivo, the release of SRS-A, but not of histamine, mediated by a nonreaginic antibody in the peritoneal cavity of sensitized rats was inhibited by KC-404 at oral doses above 3 mg/kg. In a similar anaphylactic reaction but mediated by a reaginic antibody, KC-404 also inhibited SRS-A release at intraperitoneal doses of 2.5 to 10 mg/kg. The inhibitory activity on histamine release was less than half of that on SRS-A release. These results indicate that KC-404 is an orally active compound with a unique mode of action to inhibit preferentially both the effects and immunological release of SRS-A.

摘要

一种新型化合物3-异丁酰基-2-异丙基吡唑并[1,5-a]吡啶(KC-404)作为潜在抗过敏剂的作用模式已被研究。KC-404在体外豚鼠气管和体内麻醉豚鼠中显示出直接的支气管扩张活性。此外,KC-404在体外对豚鼠回肠的过敏反应慢反应物质(SRS-A)具有相当选择性的拮抗作用。在麻醉豚鼠中,静脉注射和十二指肠内注射KC-404抑制SRS-A诱导的支气管收缩的半数有效剂量(ED50)分别为0.0014和0.0065 mg/kg。抑制组胺或特别是乙酰胆碱引起的支气管痉挛需要更高的剂量。口服0.001至0.1 mg/kg的KC-404对豚鼠和大鼠皮内注射SRS-A引起的血管通透性增加也显示出选择性抑制作用。KC-404在体外以10(-8)至10(-4) g/ml的浓度抑制致敏豚鼠切碎肺中介质的免疫释放,特别是SRS-A的释放。在体内,口服剂量高于3 mg/kg时,KC-404可抑制致敏大鼠腹腔中非反应素抗体介导的SRS-A释放,但不抑制组胺释放。在类似的由反应素抗体介导的过敏反应中,腹腔注射2.5至10 mg/kg的KC-404也可抑制SRS-A释放。其对组胺释放的抑制活性不到对SRS-A释放抑制活性的一半。这些结果表明,KC-404是一种口服活性化合物,具有独特的作用模式,能优先抑制SRS-A的作用和免疫释放。

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