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2β-碳(2-[F]氟乙氧基)-3β-(3´-(()-2-碘乙烯基)苯基)降托烷 (注:原文括号处表述不太清晰准确,可能影响对完整准确化学名称的理解)

2β-Carbo(2-[F]fluoroethoxy)-3β-(3´-(()-2-iodoethenyl)phenyl)nortropane

作者信息

Stehouwer Jeffrey, Chopra Arvind

机构信息

Department of Radiology,, Center for Systems Imaging,, Emory University

National Center for Biotechnology Information, NLM, NIH, Bethesda, MD 20894

Abstract

Serotonin (5-hydroxytryptamine (5HT)) is a neurotransmitter that is transported across the cell membrane by the serotonin transporter (SERT or 5HTT) (1) and is expressed in several tissues of the body, such as those of the brain, lungs (2-4), bone (5, 6), gastrointestinal tract (7), blood platelets (8, 9), and the cardiovascular system (10-12). Within the brain, the SERT is present primarily on the presynaptic neurons (13-15), and a high density of these transporters has been detected in the caudate, putamen, thalamus, hypothalamus, midbrain, pons, medulla, and amygdala; by comparison, the cortex has a lower density of the transporter (16-22). Alterations in serotonergic neurotransmission and SERT density in the brain have been implicated in the pathophysiology of depression and schizophrenia and may lead to suicide (23-26). Investigators have developed and evaluated the biological activity of several selective serotonin reuptake inhibitors (SSRIs)as for the treatment of these neurological conditions (27-30). Several SSRIs approved by the United States Food and Drug Administration (FDA) are available commercially for the treatment of SERT-related conditions. Positron emission tomography (PET) imaging is often used as an investigational tool to measure the SERT density and SSRI occupancy of the transporter (because these are not FDA approved biomarkers) (31-33), and it is considered a suitable technique to study the pathophysiology of depression and to develop (34-36) or monitor (37) the efficacy of new SERT therapeutics. In a continuing effort to develop tracer probes for the visualization of SERT with PET imaging techniques, Stehouwer et al. synthesized a F-labeled compound, 2β-carbo(2-[F]fluoroethoxy)-3β-(3´-(()-2-iodoethenyl)phenyl) nortropane ([F]FEZIENT), and evaluated the radiolabel for the detection of the SERT in non-human primates (38).

摘要

血清素(5-羟色胺,5HT)是一种神经递质,它通过血清素转运体(SERT或5HTT)穿过细胞膜进行转运(1),并在身体的多个组织中表达,如大脑、肺(2 - 4)、骨骼(5, 6)、胃肠道(7)、血小板(8, 9)和心血管系统(10 - 12)。在大脑中,SERT主要存在于突触前神经元上(13 - 15),在尾状核、壳核、丘脑、下丘脑、中脑、脑桥、延髓和杏仁核中检测到这些转运体的高密度分布;相比之下,皮质中转运体的密度较低(16 - 22)。大脑中血清素能神经传递和SERT密度的改变与抑郁症和精神分裂症的病理生理学有关,可能导致自杀(23 - 26)。研究人员已开发并评估了几种选择性血清素再摄取抑制剂(SSRI)的生物活性,用于治疗这些神经系统疾病(27 - 30)。美国食品药品监督管理局(FDA)批准的几种SSRI已在市场上用于治疗与SERT相关的疾病。正电子发射断层扫描(PET)成像常被用作一种研究工具,以测量转运体的SERT密度和SSRI占有率(因为这些不是FDA批准的生物标志物)(31 - 33),并且它被认为是研究抑郁症病理生理学以及开发(34 - 36)或监测(37)新型SERT治疗药物疗效的合适技术。为了继续努力开发用于PET成像技术可视化SERT的示踪探针,Stehouwer等人合成了一种F标记的化合物,2β - 碳(2 - [F]氟乙氧基)- 3β - (3´ - (() - 2 - 碘乙烯基)苯基)降托烷([F]FEZIENT),并评估了该放射性标记物在非人灵长类动物中检测SERT的情况(38)。

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