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(R)-N-甲基-3-(3-(125)I-吡啶-2-氧基)-3-苯基丙-1-胺:一种用于去甲肾上腺素转运体的新型探针。

(R)-N-Methyl-3-(3-(125)I-pyridin-2-yloxy)-3-phenylpropan-1-amine: a novel probe for norepinephrine transporters.

作者信息

Lakshmi Balagopal, Kung Mei-Ping, Lieberman Brian, Zhao Jun, Waterhouse Rikki, Kung Hank F

机构信息

Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Nucl Med Biol. 2008 Jan;35(1):43-52. doi: 10.1016/j.nucmedbio.2007.08.007. Epub 2007 Nov 19.

Abstract

Alterations in serotonin and norepinephrine neuronal functions have been observed in patients with major depression. Several antidepressants bind to both serotonin transporters and norepinephrine transporters (NET). The ability to image NET in the human brain would be a useful step toward understanding how alterations in NET relate to disease. In this study, we report the synthesis and characterization of a new series of derivatives of iodonisoxetine, a known radioiodinated probe. The most promising, (R)-N-methyl-3-(3-iodopyridin-2-yloxy)-3-phenylpropylamine (PYINXT), displayed a high and saturable binding to NET, with a K(d) value of 0.53+/-0.03 nM. Biodistribution studies of (R)-N-methyl-3-(3-(125)I-pyridin-2-yloxy)-3-phenylpropan-1-amine in rats showed moderate initial brain uptake (0.54% dose/organ at 2 min) with a relatively fast washout from the brain (0.16% dose/organ at 2 h) as compared to [(125)I]INXT. The hypothalamus (a NET-rich region)-to-striatum (a region devoid of NET) ratio was found to be 2.14 at 4 h after intravenous injection. Preliminary results suggest that this improved iodinated ligand, when labeled with (123)I, may be useful for mapping NET-binding sites with single photon emission computed tomography in the living human brain.

摘要

在重度抑郁症患者中已观察到血清素和去甲肾上腺素神经元功能的改变。几种抗抑郁药可同时结合血清素转运体和去甲肾上腺素转运体(NET)。对人脑中NET进行成像的能力将是朝着理解NET的改变与疾病之间的关系迈出的有益一步。在本研究中,我们报告了一系列已知的放射性碘化探针碘诺西汀新衍生物的合成与表征。最有前景的(R)-N-甲基-3-(3-碘吡啶-2-基氧基)-3-苯基丙胺(PYINXT)对NET表现出高亲和力且可饱和结合,其解离常数(K(d))值为0.53±0.03 nM。对(R)-N-甲基-3-(3-(125)I-吡啶-2-基氧基)-3-苯基丙-1-胺在大鼠中的生物分布研究表明,与[(125)I]INXT相比,其在脑中的初始摄取量适中(2分钟时为0.54%剂量/器官),且从脑中清除相对较快(2小时时为0.16%剂量/器官)。静脉注射后4小时,下丘脑(富含NET的区域)与纹状体(缺乏NET的区域)的比值为2.14。初步结果表明,这种经过改进的碘化配体,用(123)I标记后,可能有助于在活体人脑中用单光子发射计算机断层扫描绘制NET结合位点。

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PET imaging of norepinephrine transporters.去甲肾上腺素转运体的正电子发射断层显像
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