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首页> 外文期刊>Pulmonary pharmacology & therapeutics >The triple neurokinin-receptor antagonist CS-003 inhibits neurokinin A-induced bronchoconstriction in patients with asthma.
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The triple neurokinin-receptor antagonist CS-003 inhibits neurokinin A-induced bronchoconstriction in patients with asthma.

机译:三联神经激肽受体拮抗剂CS-003抑制哮喘患者神经激肽A诱导的支气管收缩。

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摘要

Neurokinin A (NKA) causes bronchoconstriction in asthmatic patients. In vitro both NK1 and NK2 receptors can mediate airway contraction. Moreover in guinea pigs, NK3 receptors facilitate cholinergic neurotransmission. Dual tachykinin NK1/NK2 receptor antagonism results in prevention of NKA-induced bronchoconstriction. We have now examined the effect of a single dose of the triple tachykinin receptor antagonist CS-003 on NKA-induced bronchoconstriction in asthmatics. A double blind, crossover, placebo-controlled trial in 16 mild asthmatics was performed. One single dose of CS-003 (200 mg, solution in distilled water) or matched placebo was given orally on the assessment days. NKA-provocation tests were performed pre-dose and 1, 8 and 24 h after dosing. There was a significant shift to the right of the dose-response curve at 1 and 8 h after intake of CS-003. PC20 was not reached in 12/16 patients at 1h post-dose and in 5/16 patients at 8 h post-dose. This did not occur under placebo treatment. A single dose of 200 mg CS-003 protected significantly against NKA-induced bronchoconstriction at 1 and 8h post-dose in mild asthmatics.
机译:神经激肽A(NKA)引起哮喘患者的支气管收缩。在体外,NK1和NK2受体均可介导气道收缩。此外,在豚鼠中,NK3受体促进胆碱能神经传递。速激肽NK1 / NK2受体双重拮抗作用可预防NKA诱导的支气管收缩。现在我们已经研究了单剂量三联速激肽受体拮抗剂CS-003对NKA诱导的哮喘支气管收缩的作用。在16例轻度哮喘患者中进行了一项双盲,交叉,安慰剂对照试验。在评估日口服一剂CS-003(200 mg,在蒸馏水中的溶液)或匹配的安慰剂。给药前,给药后1、8和24小时进行NKA激发试验。摄入CS-003后1和8小时,剂量反应曲线的右侧有明显变化。给药后1h的12/16患者和给药后8h的5/16患者未达到PC20。在安慰剂治疗下没有发生这种情况。在轻度哮喘患者中,单剂200 mg CS-003在用药后1和8h可以明显预防NKA诱导的支气管收缩。

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