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[KC - 404对支气管过敏反应的影响]

[Effects of KC-404 on bronchial anaphylactic reactions].

作者信息

Nishino K, Ohashi M, Hara S, Suzuki S, Irikura T

出版信息

Nihon Yakurigaku Zasshi. 1984 Apr;83(4):281-9.

PMID:6745809
Abstract

The effects of 3-isobutyryl-2-isopropylpyrazolo [1,5-a] pyridine (KC-404), a new anti-allergic agent with a unique mode of action, on bronchial anaphylactic reactions were investigated in guinea pigs and rats. The inhibitory effects of orally administered KC-404 on systemic anaphylactic reaction caused by intravenous antigen and on anaphylactic bronchoconstriction caused by inhaled antigen in guinea pigs actively sensitized with egg albumin were observed at doses of 100 mg/kg and 10 mg/kg, respectively. When these animals were pretreated with diphenhydramine and atropine before antigen challenge, the inhibitory effects of KC-404 were markedly enhanced; doses as low as 0.25 to 0.5 mg/kg p.o. were effective in this situation. In guinea pigs similarly sensitized as above, KC-404 injected i.v. after the maximum development of antigen-induced constriction of airways resulted in a rapid dilatation. KC-404 was about 100 times as potent as aminophylline in this respect. KC-404 inhibited passive anaphylactic bronchoconstriction in rats mediated by an IgE antibody at an oral dose of 2.5 mg/kg. The inhibitory effect of KC-404 (10 mg/kg) persisted for at least 6 hr. These results indicate that KC-404 is orally effective in inhibiting anaphylactic bronchoconstrictions mediated by IgE as well as IgG antibodies. Furthermore, KC-404 is suggested to be able to control the SRS-A-induced component of bronchospasm.

摘要

研究了具有独特作用方式的新型抗过敏药3-异丁酰基-2-异丙基吡唑并[1,5-a]吡啶(KC-404)对豚鼠和大鼠支气管过敏反应的影响。在以卵清蛋白主动致敏的豚鼠中,分别观察到口服100 mg/kg和10 mg/kg的KC-404对静脉注射抗原引起的全身过敏反应以及吸入抗原引起的过敏性支气管收缩的抑制作用。当在抗原攻击前用苯海拉明和阿托品预处理这些动物时,KC-404的抑制作用明显增强;在这种情况下,低至0.25至0.5 mg/kg口服给药有效。在上述类似致敏的豚鼠中,在抗原诱导的气道收缩达到最大程度后静脉注射KC-404导致迅速扩张。在这方面,KC-404的效力约为氨茶碱的100倍。KC-404以2.5 mg/kg的口服剂量抑制大鼠中由IgE抗体介导的被动过敏性支气管收缩。KC-404(10 mg/kg)的抑制作用持续至少6小时。这些结果表明,KC-404口服可有效抑制由IgE以及IgG抗体介导的过敏性支气管收缩。此外,提示KC-404能够控制SRS-A诱导的支气管痉挛成分。

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