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药物对大鼠中葡聚糖诱导的嗜酸性粒细胞增多和肺高反应性的影响。

The effects of drugs on Sephadex-induced eosinophilia and lung hyper-responsiveness in the rat.

作者信息

Spicer B A, Baker R C, Hatt P A, Laycock S M, Smith H

机构信息

SmithKline Beecham Pharmaceuticals, Epsom, Surrey.

出版信息

Br J Pharmacol. 1990 Dec;101(4):821-8. doi: 10.1111/j.1476-5381.1990.tb14164.x.

Abstract
  1. Rats given an intravenous injection of Sephadex particles (0.5 mg of G200 in 1 ml of saline) on days 0, 2 and 5 had a blood eosinophilia which was maximal on day 7. 2. On day 7, broncho-alveolar lavage (BAL) fluids taken from the rats contained an increased number of eosinophils and fewer mononuclear cells but there was no change in the small number of neutrophils. In addition the rats were hyper-sensitive to the increase in resistance to artificial respiration produced by 5-hydroxytryptamine (5-HT), given intravenously, with a shift to the left of the log dose-response curve. Lung parenchymal strips, taken from the rats on days 6, 7 and 8, were hyper-reactive to 5-HT with an increase in slope of the log dose-response curve. 3. Compounds with a wide variety of activities were evaluated for their effects on the blood eosinophilia on day 7 when given before each injection of Sephadex. The eosinophilia was reduced by glucocorticosteroids, beta-adrenoceptor agonists, aminophylline, dapsone and phenidone. 4. Dexamethasone, isoprenaline, dapsone and phenidone at doses that reduced the blood eosinophilia also reduced the changes in number of leucocytes in the BAL fluids and the hyper-responsiveness to 5-HT in vivo and in vitro, except that the effects of dapsone on the hyper-sensitivity to 5-HT in vivo did not reach significance. Aminophylline was the least effective of the drugs at reducing the blood eosinophilia and its effects on the other changes did not reach significance. Sodium cromoglycate reduced the BAL eosinophilia but had no effect on the other changes produced by Sephadex. 5. The correlation coefficients between blood eosinophil numbers and reactivity to 5-HT in vitro and sensitivity in vivo were r = 0.76, (n = 88; P < 0.001) and r = 0.53, (n = 61; P < 0.001) respectively. 6. Doses of dexamethasone, isoprenaline, dapsone and phenidone that reduced the blood eosinophilia when given before each injection of Sephadex were inactive when given up to 8 h after the Sephadex. 7. These data show an association between blood eosinophilia and hyper-responsiveness of the lung. The blood eosinophilia in the rats was triggered within the first few hours of injecting the Sephadex and drugs have been identified which inhibit this trigger.
摘要
  1. 在第0、2和5天接受静脉注射葡聚糖颗粒(1毫升盐水中含0.5毫克G200)的大鼠出现血液嗜酸性粒细胞增多,在第7天达到峰值。2. 在第7天,从这些大鼠获取的支气管肺泡灌洗(BAL)液中嗜酸性粒细胞数量增加,单核细胞数量减少,但少量中性粒细胞数量无变化。此外,大鼠对静脉注射5-羟色胺(5-HT)引起的人工呼吸阻力增加高度敏感,对数剂量反应曲线向左偏移。在第6、7和8天从大鼠获取的肺实质条对5-HT反应性增强,对数剂量反应曲线斜率增加。3. 评估了具有多种活性的化合物在每次注射葡聚糖前给药时对第7天血液嗜酸性粒细胞增多的影响。糖皮质激素、β-肾上腺素受体激动剂、氨茶碱、氨苯砜和非那吡啶可减轻嗜酸性粒细胞增多。4. 地塞米松、异丙肾上腺素、氨苯砜和非那吡啶在降低血液嗜酸性粒细胞增多的剂量下,也减少了BAL液中白细胞数量的变化以及体内和体外对5-HT的高反应性,但氨苯砜对体内5-HT高敏感性的影响未达到显著水平。氨茶碱在减轻血液嗜酸性粒细胞增多方面是效果最差的药物,其对其他变化的影响未达到显著水平。色甘酸钠减少了BAL嗜酸性粒细胞增多,但对葡聚糖产生的其他变化无影响。5. 血液嗜酸性粒细胞数量与体外对5-HT的反应性以及体内敏感性之间的相关系数分别为r = 0.76,(n = 88;P < 0.001)和r = 0.53,(n = 61;P < 0.001)。6. 在每次注射葡聚糖前给药时可降低血液嗜酸性粒细胞增多的地塞米松、异丙肾上腺素、氨苯砜和非那吡啶剂量,在葡聚糖注射后8小时内给药则无活性。7. 这些数据表明血液嗜酸性粒细胞增多与肺的高反应性之间存在关联。大鼠的血液嗜酸性粒细胞增多在注射葡聚糖后的最初几小时内引发,并且已鉴定出可抑制这种触发的药物。

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