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1
Measurement of activity of 5-HT antagonists following oral administration in man: a comparison of methysergide and BW501.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
Br J Clin Pharmacol. 1979 Feb;7(2):197-9. doi: 10.1111/j.1365-2125.1979.tb00921.x.
2
The effects of a selective 5-HT2 receptor antagonist (ICI 170,809) on platelet aggregation and pupillary responses in healthy volunteers.一种选择性5-羟色胺2(5-HT2)受体拮抗剂(ICI 170,809)对健康志愿者血小板聚集和瞳孔反应的影响。
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4
Effect of 5-hydroxytryptamine antagonist on gastric secretion in albino rats.5-羟色胺拮抗剂对白化病大鼠胃液分泌的影响。
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本文引用的文献

1
Aggregation of blood platelets by adenosine diphosphate and its reversal.二磷酸腺苷引起的血小板聚集及其逆转
Nature. 1962 Jun 9;194:927-9. doi: 10.1038/194927b0.
2
An assessment of platelet aggregation induced by 5-hydroxytryptamine.5-羟色胺诱导的血小板聚集评估。
J Clin Pathol. 1971 Apr;24(3):250-8. doi: 10.1136/jcp.24.3.250.
3
Evaluation of the peripheral and central antagonistic activities against 5-hydroxytryptamine of some new agents.某些新型药物对5-羟色胺的外周和中枢拮抗活性评估。
Br J Pharmacol. 1970 May;39(1):223P-224P.
4
Effects of ergotamine and methysergide on blood platelet aggregation responses of migrainous subjects.麦角胺和甲基麦角新碱对偏头痛患者血小板聚集反应的影响。
J Neurol Neurosurg Psychiatry. 1974 May;37(5):593-7. doi: 10.1136/jnnp.37.5.593.

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.

DOI:10.1111/j.1365-2125.1979.tb00921.x
PMID:760752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1429433/
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。