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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。

The effects of a selective 5-HT2 receptor antagonist (ICI 170,809) on platelet aggregation and pupillary responses in healthy volunteers.

作者信息

Millson D S, Jessup C L, Swaisland A, Haworth S, Rushton A, Harry J D

机构信息

ICI Pharmaceuticals, Macclesfield, Cheshire.

出版信息

Br J Clin Pharmacol. 1992 Mar;33(3):281-8. doi: 10.1111/j.1365-2125.1992.tb04036.x.

Abstract
  1. ICI 170,809 (2-(2-dimethylamino-2-methylpropylthio)-3-phenylquinoline hydrochloride) is a potent 5-hydroxytryptamine (5-HT) type 2 postsynaptic receptor antagonist. 2. Effects of ICI 170,809 as single oral doses (3, 7, 15 and 30 mg) or placebo were studied on the duration of antagonism for the ex vivo platelet aggregatory response to 5-HT and to the pupillary light constrictor response in eight healthy male volunteers. 3. Pupillary dark adapted responses to a 0.5 s light stimulus were measured using a portable infrared pupillometer, for up to 24 h after dosing. 4. The in vitro platelet 5-HT aggregation response was reduced by ICI 170,809, with depression of the dose-response curve to 5-HT at all concentrations of 5-HT and with no evidence for a parallel shift. 5. The ex vivo platelet 5-HT response demonstrated a dose related significant (P less than 0.02) decrease in aggregation reaching a maximum at 2 h after dosing with the effect persisting for at least 8 h after dosing with the 7 and 15 mg doses. 6. Resting pupil diameter (RPD), and light induced pupillary responses in the dark adapted pupil, showed a significant (P less than 0.01) dose related reduction with significant (P less than 0.05) effects still present with the 15 and 30 mg doses at 8 h after dosing. 7. We conclude that, changes in both ex vivo platelet aggregation to 5-HT and dark adapted pupil size, are significantly correlated (P less than 0.0001) with log plasma concentrations (ng ml-1) of ICI 170,809, enabling the assessment of 5-HT2-receptor antagonism in man.
摘要
  1. ICI 170,809(2-(2-二甲基氨基-2-甲基丙基硫代)-3-苯基喹啉盐酸盐)是一种强效的5-羟色胺(5-HT)2型突触后受体拮抗剂。2. 研究了ICI 170,809单次口服剂量(3、7、15和30毫克)或安慰剂对8名健康男性志愿者体内5-HT体外血小板聚集反应和瞳孔光收缩反应的拮抗持续时间的影响。3. 使用便携式红外瞳孔计测量给药后长达24小时的瞳孔暗适应对0.5秒光刺激的反应。4. ICI 170,809降低了体外血小板5-HT聚集反应,在所有5-HT浓度下剂量反应曲线均向5-HT方向下移,且无平行位移的证据。5. 体外血小板5-HT反应显示聚集有剂量相关的显著降低(P小于0.02),给药后2小时达到最大值,7毫克和15毫克剂量给药后效应至少持续8小时。6. 静息瞳孔直径(RPD)以及暗适应瞳孔的光诱导瞳孔反应显示有剂量相关的显著降低(P小于0.01),给药后8小时15毫克和30毫克剂量仍有显著(P小于0.05)效应。7. 我们得出结论,体外血小板对5-HT的聚集变化和暗适应瞳孔大小变化与ICI 170,809的血浆浓度对数(纳克/毫升)显著相关(P小于0.0001),从而能够评估人体中的5-HT2受体拮抗作用。

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