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使用正电子发射断层扫描和[11C]WAY-100635对抑郁症成年患者在抗抑郁药物治疗前后的5-HT1A受体结合情况进行测量。

Measurement of 5-HT1A receptor binding in depressed adults before and after antidepressant drug treatment using positron emission tomography and [11C]WAY-100635.

作者信息

Moses-Kolko Eydie L, Price Julie C, Thase Michael E, Meltzer Carolyn Cidis, Kupfer David J, Mathis Chester A, Bogers Wendy D, Berman Susan R, Houck Patricia R, Schneider Trisha N, Drevets Wayne C

机构信息

Departments of Psychiatry, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

出版信息

Synapse. 2007 Jul;61(7):523-30. doi: 10.1002/syn.20398.

DOI:10.1002/syn.20398
PMID:17447260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4448112/
Abstract

OBJECTIVE

To assess effects of chronic antidepressant drug treatment on serotonin type-1A receptor (5-HT(1A)R) binding potential (BP) in major depressive disorder.

METHODS

Depressed subjects (n = 27) were imaged using PET and [(11)C]WAY-100635 at baseline and following a median of 9.4 weeks of treatment with selective serotonin reuptake inhibitor or dual reuptake inhibitor antidepressant agents. Fifteen subjects had complete pre- and post-treatment scan data. The 5-HT(1A)R BP was derived from the tissue time-radioactivity concentrations from regions-of-interest defined a priori, using a simplified reference tissue model (SRTM), and in a subset of subjects, compartmental modeling (CMOD).

RESULTS

Chronic treatment had no effect on pre- or post-synaptic 5-HT(1A)R BP, as confirmed by both the SRTM and CMOD analyses. These results were unaffected by treatment response status and were consistent across brain regions. Among the 22 subjects for whom the clinical response-to-treatment was established, the treatment nonresponders (n = 7) had higher baseline BP values in the left (P = 0.01) and right orbital cortex (P = 0.02) than the responders (n = 15).

CONCLUSIONS

Chronic antidepressant drug treatment did not significantly change cerebral 5-HT(1A)R binding, consistent with preclinical evidence that the alterations in serotonergic function associated with antidepressant drug administration are not accompanied by changes in 5-HT(1A)R density. Higher baseline 5-HT(1A)R binding was associated with poorer response to treatment.

摘要

目的

评估慢性抗抑郁药物治疗对重度抑郁症患者5-羟色胺1A受体(5-HT(1A)R)结合潜能(BP)的影响。

方法

对27名抑郁症患者在基线期以及在接受选择性5-羟色胺再摄取抑制剂或双重再摄取抑制剂抗抑郁药治疗中位数为9.4周后,使用正电子发射断层扫描(PET)和[(11)C]WAY-100635进行成像。15名受试者有完整的治疗前和治疗后扫描数据。5-HT(1A)R BP是根据预先定义的感兴趣区域的组织时间-放射性浓度,使用简化参考组织模型(SRTM)得出的,在部分受试者中还采用了房室模型(CMOD)。

结果

慢性治疗对突触前或突触后5-HT(1A)R BP均无影响,SRTM和CMOD分析均证实了这一点。这些结果不受治疗反应状态的影响,且在各脑区均一致。在确定了临床治疗反应的22名受试者中,治疗无反应者(n = 7)左侧(P = 0.01)和右侧眶额皮质(P = 0.02)的基线BP值高于有反应者(n = 15)。

结论

慢性抗抑郁药物治疗并未显著改变大脑5-HT(1A)R结合,这与临床前证据一致,即与抗抑郁药物给药相关的5-羟色胺能功能改变并未伴随5-HT(1A)R密度的变化。较高的基线5-HT(1A)R结合与较差的治疗反应相关。

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