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血小板活化因子拮抗剂(BN 52063)对运动诱发性哮喘期间支气管收缩和血小板活化的影响。

Effects of a PAF-antagonist (BN 52063) on bronchoconstriction and platelet activation during exercise induced asthma.

作者信息

Wilkens J H, Wilkens H, Uffmann J, Bövers J, Fabel H, Frölich J C

机构信息

Department of Clinical Pharmacology, Hannover Medical School, FRG.

出版信息

Br J Clin Pharmacol. 1990 Jan;29(1):85-91. doi: 10.1111/j.1365-2125.1990.tb03606.x.

Abstract
  1. The effects of a specific PAF acether antagonist (BN 52063) on the response to isocapnic hyperventilation with dry cold air (ISH study) and exercise (EIA study) were assessed in a single dose and short term treatment study in 10 patients with exercise induced asthma. 2. ISH challenge was performed twice within 1 h after administration of either placebo, 240 mg BN 52063 p.o. or inhalation of 2.4 mg BN 52063. Hyperventilation increased Raw from 0.30 +/- 0.02 to 0.89 kPa s l-1 (P less than 0.001) after the first challenge and from 0.28 +/- 0.04 to 0.84 +/- 0.06 kPa s l-1 (P less than 0.001) after the second challenge. Oral pretreatment with BN 52063 did not result in a reduction of bronchoconstriction during both challenges. A significant increase of Raw was noted immediately after inhalation of BN 52063. An inhibition of PAF induced platelet aggregation (by a factor of 2) occurred after oral administration of BN 52063 after both ISH challenges (P less than 0.05). No significant inhibition of PAF induced platelet aggregation was seen after inhalation of BN 52063. At concentrations up to 30 microM in vitro, BN 52063 inhibited PAF induced platelet aggregation in a dose dependent manner. The IC50 of BN 52063 against the aggregating effect of 1 microM PAF was 7.0 +/- 2.1 microM. 3. In the EIA study the patients were challenged on the third day of treatment with either placebo or 240 mg BN 52063 p.o. or 5 mg BN 52063 by inhalation. Peak expiratory flow rates (PEFR) fell by 155 +/- 37 1 min-1 after exercise.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 在一项针对10名运动诱发性哮喘患者的单剂量短期治疗研究中,评估了一种特定的血小板活化因子乙酰醚拮抗剂(BN 52063)对冷空气等容过度通气反应(ISH研究)和运动反应(EIA研究)的影响。2. 在给予安慰剂、口服240毫克BN 52063或吸入2.4毫克BN 52063后1小时内,进行两次ISH激发试验。第一次激发试验后,过度通气使气道阻力从0.30±0.02增加到0.89千帕·秒·升⁻¹(P<0.001),第二次激发试验后从0.28±0.04增加到0.84±0.06千帕·秒·升⁻¹(P<0.001)。口服BN 52063预处理在两次激发试验期间均未导致支气管收缩减轻。吸入BN 52063后立即观察到气道阻力显著增加。在两次ISH激发试验后口服BN 52063后,PAF诱导的血小板聚集受到抑制(抑制因子为2)(P<0.05)。吸入BN 52063后未观察到对PAF诱导的血小板聚集有显著抑制作用。在体外浓度高达30微摩尔时,BN 52063以剂量依赖方式抑制PAF诱导的血小板聚集。BN 52063对1微摩尔PAF聚集作用的IC50为7.0±2.1微摩尔。3. 在EIA研究中,患者在治疗的第三天接受安慰剂、口服240毫克BN 52063或吸入5毫克BN 52063激发试验。运动后呼气峰值流速(PEFR)下降了155±37升·分钟⁻¹。(摘要截短至250字)

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