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香烟烟雾诱导豚鼠气道对组胺和柠檬酸反应性的变化。

Cigarette smoke-induced changes in guinea-pig airway responsiveness to histamine and citric acid.

作者信息

Karlsson J A, Zackrisson C, Sjölin C, Forsberg K

机构信息

AB Draco, Lund, Sweden.

出版信息

Acta Physiol Scand. 1991 May;142(1):119-25. doi: 10.1111/j.1748-1716.1991.tb09136.x.

DOI:10.1111/j.1748-1716.1991.tb09136.x
PMID:1877360
Abstract

The effect of 50 min cigarette smoke exposure on airway responsiveness to the bronchoconstrictor and tussive effects of histamine and citric acid has been examined in guinea-pigs. Intravenous histamine increased intratracheal pressure (ITP) in anaesthetized guinea-pigs and the dose-response curve was significantly (P less than 0.05) steeper in cigarette smoke- than in air-exposed animals. ED50 values were 11.4 nmol kg-1 (7.4-16.8, 95% confidence interval) and 42.5 nmol kg-1 (28.8-61.4, 95% confidence interval), respectively (P less than 0.05) in smoke- and air-exposed guinea-pigs indicating an enhanced reactivity. However, the sensitivity to intravenous histamine was not changed by the cigarette smoke exposure, and the maximum increase in intratracheal pressure was the same as in control animals (air: 247 +/- 21%, n = 4; smoke: 223 +/- 18%, n = 7). The cigarette smoke-induced hyperresponsiveness to intravenous histamine was not altered by pretreatment with nebulized lidocaine (0.20 M), ipratropium bromide (0.30 mM) or cromoglycate (0.06 M), suggesting that a neural reflex is unlikely to be involved in the development of hyperresponsiveness. Conscious, smoke-exposed guinea-pigs had a significantly (P less than 0.001) reduced responsiveness to citric acid (0.40 M) and cigarette smoke. Both cough and bronchoconstriction were suppressed for about 1 h, but unchanged 24 h after exposure. The hyporesponsiveness to citric acid was inhibited by atropine (1.4 mumol kg-1 i.p.) and may therefore, at least in part, be due to increased airway secretions. The present data demonstrate that inhalation of cigarette smoke may alter guinea-pig airway responsiveness to tussive and bronchoconstrictor stimuli.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在豚鼠中研究了50分钟香烟烟雾暴露对气道对支气管收缩剂的反应性以及组胺和柠檬酸的咳嗽效应的影响。静脉注射组胺可增加麻醉豚鼠的气管内压(ITP),与暴露于空气的动物相比,暴露于香烟烟雾的动物的剂量-反应曲线明显更陡峭(P<0.05)。暴露于烟雾和空气的豚鼠的ED50值分别为11.4 nmol kg-1(7.4-16.8,95%置信区间)和42.5 nmol kg-1(28.8-61.4,95%置信区间)(P<0.05),表明反应性增强。然而,香烟烟雾暴露并未改变对静脉注射组胺的敏感性,气管内压的最大增加与对照动物相同(空气组:247±21%,n = 4;烟雾组:223±18%,n = 7)。雾化利多卡因(0.20 M)、异丙托溴铵(0.30 mM)或色甘酸(0.06 M)预处理并未改变香烟烟雾诱导的对静脉注射组胺的高反应性,这表明高反应性的发展不太可能涉及神经反射。清醒的、暴露于烟雾的豚鼠对柠檬酸(0.40 M)和香烟烟雾的反应性显著降低(P<0.001)。咳嗽和支气管收缩均被抑制约1小时,但暴露后24小时未改变。对柠檬酸的低反应性被阿托品(1.4 μmol kg-1腹腔注射)抑制,因此至少部分可能是由于气道分泌物增加所致。目前的数据表明,吸入香烟烟雾可能会改变豚鼠气道对咳嗽和支气管收缩刺激的反应性。(摘要截短至250字)

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