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在健康受试者中,通过单光子发射计算机断层扫描(SPECT)和[123I]ADAM对给予不同剂量艾司西酞普兰或西酞普兰后的血清素转运体占有率进行体内成像。

In vivo imaging of serotonin transporter occupancy by means of SPECT and [123I]ADAM in healthy subjects administered different doses of escitalopram or citalopram.

作者信息

Klein N, Sacher J, Geiss-Granadia T, Attarbaschi T, Mossaheb N, Lanzenberger R, Pötzi C, Holik A, Spindelegger C, Asenbaum S, Dudczak R, Tauscher J, Kasper S

机构信息

Department of General Psychiatry, University Hospital for Psychiatry, Währinger Gürtel, 18-20A-1090, Vienna, Austria.

出版信息

Psychopharmacology (Berl). 2006 Oct;188(3):263-72. doi: 10.1007/s00213-006-0486-0. Epub 2006 Sep 6.

Abstract

BACKGROUND

Escitalopram is a dual serotonin reuptake inhibitor (SSRI) approved for the treatment of depression and anxiety disorders. It is the S-enantiomer of citalopram, and is responsible for the serotonin reuptake activity, and thus for its pharmacological effects. Previous studies pointed out that clinically efficacious doses of other SSRIs produce an occupancy of the serotonin reuptake transporter (SERT) of about 80% or more. The novel radioligand [123I]ADAM and single photon emission computer tomography (SPECT) were used to measure midbrain SERT occupancies for different doses of escitalopram and citalopram.

METHODS

Twenty-five healthy subjects received a single dose of escitalopram [5 mg (n=5), 10 mg (n=5), and 20 mg (n=5)] or citalopram [(10 mg (n=5) and 20 mg (n=5)]. Midbrain SERT binding was measured with [(123)I]ADAM and SPECT on two study days, once without study drug and once 6 h after single dose administration of the study drug. The ratio of midbrain-cerebellum/cerebellum was the outcome measure (V3") for specific binding to SERT in midbrain. Subsequently, SERT occupancy levels were calculated using the untreated baseline level for each subject. An Emax model was used to describe the relationship between S-citalopram concentrations and SERT occupancy values. Additionally, four subjects received placebo to determine test-retest variability.

RESULTS

Single doses of 5, 10, or 20 mg escitalopram led to a mean SERT occupancy of 60+/-6, 64+/-6, and 75+/-5%, respectively. SERT occupancies for subjects treated with single doses of 10 and 20 mg citalopram were 65+/-10 and 70+/-6%, respectively. A statistically significant difference was found between SERT occupancies after application of 10 and 20 mg escitalopram, but not for 10 and 20 mg citalopram. There was no statistically significant difference between the SERT occupancies of either 10 mg citalopram or 10 mg escitalopram, or between 20 mg citalopram and 20 mg escitalopram. Emax was slightly higher after administration of citalopram (84%) than escitalopram (79%). In the test-retest study, a mean SERT "occupancy" of 4% was found after administration of placebo, the intraclass correlation coefficient was 0.92, and the repeatability coefficient was 0.25.

CONCLUSION

SPECT and [123I]ADAM were used to investigate SERT occupancies after single doses of escitalopram or citalopram. The test-retest study revealed good reproducibility of SERT quantification. Similar SERT occupancies were found after administration of equal doses (in respect to mg) of escitalopram and citalopram, giving indirect evidence for a fractional blockade of SERT by the inactive R-citalopram.

摘要

背景

艾司西酞普兰是一种双重血清素再摄取抑制剂(SSRI),被批准用于治疗抑郁症和焦虑症。它是西酞普兰的S-对映体,负责血清素再摄取活性,从而产生其药理作用。先前的研究指出,其他SSRI的临床有效剂量会使血清素再摄取转运体(SERT)的占有率达到约80%或更高。新型放射性配体[123I]ADAM和单光子发射计算机断层扫描(SPECT)被用于测量不同剂量艾司西酞普兰和西酞普兰的中脑SERT占有率。

方法

25名健康受试者接受单剂量的艾司西酞普兰[5毫克(n = 5)、10毫克(n = 5)和20毫克(n = 5)]或西酞普兰[(10毫克(n = 5)和20毫克(n = 5)]。在两个研究日,用[(123)I]ADAM和SPECT测量中脑SERT结合情况,一次在未服用研究药物时,一次在单剂量服用研究药物6小时后。中脑-小脑/小脑的比值是中脑SERT特异性结合的结果测量指标(V3")。随后,使用每个受试者未治疗的基线水平计算SERT占有率。采用Emax模型描述S-西酞普兰浓度与SERT占有率值之间的关系。此外,4名受试者接受安慰剂以确定重测变异性。

结果

单剂量5、10或20毫克的艾司西酞普兰导致平均SERT占有率分别为60±6%、64±6%和75±5%。单剂量10和20毫克西酞普兰治疗的受试者的SERT占有率分别为65±10%和70±6%。在应用10和20毫克艾司西酞普兰后,SERT占有率之间存在统计学显著差异,但10和20毫克西酞普兰之间没有。10毫克西酞普兰或10毫克艾司西酞普兰的SERT占有率之间,以及20毫克西酞普兰和20毫克艾司西酞普兰之间均无统计学显著差异。服用西酞普兰后Emax(84%)略高于艾司西酞普兰(79%)。在重测研究中,服用安慰剂后平均SERT“占有率”为4%,组内相关系数为0.92,重复性系数为0.25。

结论

SPECT和[123I]ADAM被用于研究单剂量艾司西酞普兰或西酞普兰后的SERT占有率。重测研究显示SERT定量具有良好的可重复性。给予等量(按毫克计)的艾司西酞普兰和西酞普兰后,发现SERT占有率相似,这间接证明了无活性的R-西酞普兰对SERT的部分阻断作用。

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