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色甘酸钠对麻醉豚鼠在吲哚美辛给药后组胺所致肺部反应的抑制作用。

Inhibitory effect of sodium cromoglycate on pulmonary responses to histamine administered after indomethacin in anaesthetized guinea-pigs.

作者信息

Mitchell H W

机构信息

Department of Physiology, University of Western Australia, Nedlands.

出版信息

Br J Pharmacol. 1988 Jun;94(2):515-21. doi: 10.1111/j.1476-5381.1988.tb11555.x.

Abstract
  1. Histamine (2-4 micrograms kg-1 i.v.) increased airways resistance (Raw) and decreased dynamic lung compliance (Cdyn) in urethane-anaesthetized guinea-pigs. The effects on Raw were almost abolished by atropine (0.1 mg kg-1 i.v.) and reduced by vagal cooling (11-16 degrees C). 2. Histamine-induced changes in Raw and Cdyn were significantly (P less than 0.05) enhanced by indomethacin (1 mg kg-1 i.v.). 3. In animals not treated with indomethacin, exposure to an aerosol containing sodium cromoglycate (0.01-2% for 30 s) failed to affect subsequent (3 min) histamine-induced bronchoconstriction. 4. Administration of an aerosol containing low (0.01-0.2%) concentrations of sodium cromoglycate had no effect on the enhanced responses (i.e. hyperreactivity) seen after indomethacin. However, more concentrated sodium cromoglycate aerosols (greater than 0.2%) reduced or abolished the hyperreactivity to histamine seen after indomethacin. 5. It was concluded that sodium cromoglycate can prevent the development of hyperreactivity to histamine, possibly by interacting with some mechanism utilized by both histamine and indomethacin in this model.
摘要
  1. 组胺(静脉注射2 - 4微克/千克)可增加氨基甲酸乙酯麻醉的豚鼠的气道阻力(Raw)并降低动态肺顺应性(Cdyn)。阿托品(静脉注射0.1毫克/千克)几乎可消除对Raw的影响,而迷走神经冷却(11 - 16摄氏度)可使其降低。2. 吲哚美辛(静脉注射1毫克/千克)可显著(P小于0.05)增强组胺引起的Raw和Cdyn的变化。3. 在未用吲哚美辛处理的动物中,暴露于含色甘酸钠的气雾剂(0.01 - 2%,持续30秒)未能影响随后(3分钟)组胺引起的支气管收缩。4. 给予含低浓度(0.01 - 0.2%)色甘酸钠的气雾剂对吲哚美辛后出现的增强反应(即高反应性)无影响。然而,浓度更高的色甘酸钠气雾剂(大于0.2%)可降低或消除吲哚美辛后出现的对组胺的高反应性。5. 得出的结论是,色甘酸钠可能通过与该模型中组胺和吲哚美辛共同利用的某些机制相互作用,来预防对组胺高反应性的发展。

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