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可乐定对正常人和哮喘患者支气管组胺反应的影响。

Effects of clonidine on bronchial responses to histamine in normal and asthmatic subjects.

作者信息

Dinh Xuan A T, Regnard J, Matran R, Mantrand P, Advenier C, Lockhart A

机构信息

Laboratoire de Physiologie, Faculté de Médecine Cochin Port-Royal, Paris, France.

出版信息

Eur Respir J. 1988 Apr;1(4):345-50.

PMID:3396674
Abstract

Our aim was to examine the effects of clonidine (C), an agonist of central and peripheral alpha-2 adrenoceptors, on bronchomotor responsiveness to histamine (H). In a double-blind study, we compared on two different days the effects of pretreatment with placebo (P) and with 200 micrograms or 150 micrograms of C given orally, in ten normal (NS) and eight asymptomatic asthmatic subjects (AS) respectively, the response to inhalation of serially increasing doses of H. On each day, five doubling doses of H (first dose = 3.5 and 1.1 mumol in NS and AS, respectively) were administered every 5 min; forced expiratory volume in one second (FEV1) was measured after each dose. The dose-response curves were compared by an analysis of variance. Clonidine caused hypotension with bradycardia in all subjects. Baseline values and pre-challenge values of FEV1 after P and C were identical on the two study days. Compared to P, C did not modify the response to H in NS but significantly increased it in AS (p less than 0.01). Our results suggest that the neural control of the airways differs in AS compared to NS and could be explained either by a decrease in sympathetic inhibitory activity or a greater responsiveness of the airways to parasympathetic stimulation and/or a higher parasympathetic tone in AS.

摘要

我们的目的是研究中枢和外周α-2肾上腺素能受体激动剂可乐定(C)对支气管对组胺(H)的运动反应性的影响。在一项双盲研究中,我们在两天内分别比较了在10名正常受试者(NS)和8名无症状哮喘受试者(AS)中,口服安慰剂(P)以及200微克或150微克可乐定(C)预处理后,对连续递增剂量组胺吸入的反应。每天每隔5分钟给予5个翻倍剂量的组胺(NS和AS的首剂分别为3.5和1.1微摩尔);每次给药后测量一秒用力呼气量(FEV1)。通过方差分析比较剂量反应曲线。可乐定在所有受试者中均引起低血压和心动过缓。在两个研究日,P和C后FEV1的基线值和激发前值相同。与P相比,C对NS中H的反应无影响,但在AS中显著增加(p<0.01)。我们的结果表明,与NS相比,AS中气道的神经控制有所不同,这可能是由于交感神经抑制活性降低、气道对副交感神经刺激的反应性增强和/或AS中副交感神经张力较高所致。

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