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人口服给药后5-羟色胺拮抗剂活性的测定:麦角新碱与BW501的比较

Measurement of activity of 5-HT antagonists following oral administration in man: a comparison of methysergide and BW501.

作者信息

O'Grady J, Peringer E, John G

出版信息

Br J Clin Pharmacol. 1979 Feb;7(2):197-9. doi: 10.1111/j.1365-2125.1979.tb00921.x.

Abstract

1 Oral doses of BW501 and methysergide administered to healthy volunteers inhibited the ex vivo platelet aggregation response to 5-hydroxytryptamine (5-HT). 2 Two volunteers received 100 mg BW501 and two received 10 mg BW501 and aggregation response was measured immediately pre drug and at 1,3 and 24 h post drug. After 100 mg BW501 the response to 5-HT was completely inhibited at all times studied, after 10 BW501 a response too small to measure was apparent at 24 h only. 3 In two randomised crossover studies subjects received either 2 mg BW501 (nine subjects), 2 mg methysergide (six subjects) or no drug (nine subjects) and aggregation response to 5-HT was measured immediately pre drug and at 1, 2, 3, 5, 7, 24 h post drug. 4 Methysergide (2 mg) produced complete inhibition of aggregation for 24 h after dosing; following 2 mg BW501 the aggregation response was significantly lower than on the control occasion at 1 (P less than 0.01), 2 (P less than 0.01) and 3 (P less than 0.05) h post drug. The response was inhibited by rr%, 31% and 16% at these times respectively. 5 It is suggested that this technique provides a suitable method for demonstration of activity of 5-HT antagonists after oral dosing in man.

摘要
  1. 给健康志愿者口服BW501和甲基麦角新碱,可抑制体外血小板对5-羟色胺(5-HT)的聚集反应。2. 两名志愿者服用100毫克BW501,两名服用10毫克BW501,在给药前及给药后1、3和24小时立即测量聚集反应。服用100毫克BW501后,在所有研究时间点对5-HT的反应均被完全抑制;服用10毫克BW501后,仅在24小时出现太小而无法测量的反应。3. 在两项随机交叉研究中,受试者分别服用2毫克BW501(9名受试者)、2毫克甲基麦角新碱(6名受试者)或不服用药物(9名受试者),并在给药前及给药后1、2、3、5、7、24小时测量对5-HT的聚集反应。4. 甲基麦角新碱(2毫克)给药后24小时产生完全聚集抑制;服用2毫克BW501后,给药后1小时(P<0.01)、2小时(P<0.01)和3小时(P<0.05)的聚集反应明显低于对照情况。这些时间点的反应分别被抑制了rr%、31%和16%。5. 有人认为,该技术为证明5-HT拮抗剂口服给药后在人体中的活性提供了一种合适的方法。

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