99mTc(CO)3-labeled 1-(2-Pyridyl)piperazine derivatives as radioligands for 5-HT7 receptors

IF 2.5 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Annals of Nuclear Medicine Pub Date : 2023-11-30 DOI:10.1007/s12149-023-01885-2
Alireza Mardanshahi, Samaneh Vaseghi, Seyed Jalal Hosseinimehr, Seyed Mohammad Abedi, Sajjad Molavipordanjani
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Abstract

Background

The 5-hydroxytryptamine receptor (5-HTR) family includes seven classes of receptors. The 5-HT7R is the newest member of this family and contributes to different physiological and pathological processes. As a pathology, glioblastoma multiform (GBM) overexpresses 5-HT7R; hence, this study aims to develop radiolabeled aryl piperazine derivatives as 5-HT7R imaging agents. 

Methods

Compounds 6 and 7 as 1-(3-nitropyridin-2-yl)piperazine derivatives were radiolabeled with fac-[99mTc(CO)3(H2O)3]+ and 99mTc(CO)3-[6] and 99mTc(CO)3-[7] were obtained with high radiochemical purity (RCP > 94%). The stability of the radiotracers was evaluated in both saline and mouse serum. Specific binding on different cell lines including U-87 MG, MCF-7, SKBR3, and HT-29 was performed. The biodistribution of these radiotracers was evaluated in normal and U-87 MG Xenografted models. Finally, 99mTc(CO)3-[6] and 99mTc(CO)3-[7] were applied for in vivo imaging in U-87 MG Xenografted models.

Results

Specific binding study indicates that 99mTc(CO)3-[6] and 99mTc(CO)3-[7] can recognize 5-HT7R of U87-MG cell line. The biodistribution study in normal mice indicates that the brain uptake of 99mTc(CO)3-[6] and 99mTc(CO)3-[7] is the highest at 30 min post-injection (0.8 ± 0.25 and 0.64 ± 0.18%ID/g, respectively). The data of the biodistribution study in the U87-MG xenograft model revealed that these radiotracers could accumulate in the tumor site, and the highest tumor uptake was observed at 60 min post-injection (3.38 ± 0.65 and 3.27 ± 0.5%ID/g, respectively). The injection of pimozide can block the tumor’s radiotracer uptake, indicating the binding of these radiotracers to the 5-HT7R. The imaging study in the xenograft model also confirms the biodistribution data. The acquired images clearly show the tumor site, and the tumor-to-muscle ratio for 99mTc(CO)3-[6] and 99mTc(CO)3-[7] at 60 min was 3.33 and 3.88, respectively. 

Conclusions

99mTc(CO)3-[6] and 99mTc(CO)3-[7] can visualize tumor in the U87-MG xenograft model  due to their affinity toward 5-HT7R.

Graphical abstract

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99mTc(CO)3标记的1-(2-吡啶基)哌嗪衍生物作为5-HT7受体的放射性配体。
背景:5-羟色胺受体(5-HTR)家族包括7类受体。5-HT7R是该家族的最新成员,参与不同的生理和病理过程。作为一种病理,多形性胶质母细胞瘤(GBM)过表达5-HT7R;因此,本研究旨在开发放射性标记芳基哌嗪衍生物作为5-HT7R显像剂。方法:用fac-[99mTc(CO)3(H2O)3]+和99mTc(CO)3-[6]和99mTc(CO)3-[7]对1-(3-硝基吡啶)哌嗪衍生物化合物6和7进行放射性标记,获得高放射化学纯度(RCP > 94%)。在生理盐水和小鼠血清中评价了放射性示踪剂的稳定性。对不同细胞系进行特异性结合,包括U-87 MG、MCF-7、SKBR3和HT-29。在正常和U-87 MG异种移植模型中评价了这些示踪剂的生物分布。最后采用99mTc(CO)3-[6]和99mTc(CO)3-[7]对U-87 MG异种移植模型进行体内显像。结果:特异性结合研究表明99mTc(CO)3-[6]和99mTc(CO)3-[7]能够识别U87-MG细胞系的5-HT7R。正常小鼠的生物分布研究表明,99mTc(CO)3-[6]和99mTc(CO)3-[7]在注射后30 min脑摄取最高(分别为0.8±0.25和0.64±0.18%ID/g)。在U87-MG异种移植物模型中的生物分布研究数据显示,这些放射性示踪剂可以在肿瘤部位积累,注射后60min时肿瘤摄取最高(分别为3.38±0.65和3.27±0.5%ID/g)。注射吡莫齐可以阻断肿瘤对放射性示踪剂的摄取,表明这些放射性示踪剂与5-HT7R结合。异种移植物模型的影像学研究也证实了生物分布数据。获得的图像清晰显示肿瘤部位,60 min时99mTc(CO)3-[6]和99mTc(CO)3-[7]的肿瘤与肌肉的比值分别为3.33和3.88。结论:99mTc(CO)3-[6]和99mTc(CO)3-[7]由于其对5-HT7R的亲和力,在U87-MG异种移植瘤模型中可见肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Nuclear Medicine
Annals of Nuclear Medicine 医学-核医学
CiteScore
4.90
自引率
7.70%
发文量
111
审稿时长
4-8 weeks
期刊介绍: Annals of Nuclear Medicine is an official journal of the Japanese Society of Nuclear Medicine. It develops the appropriate application of radioactive substances and stable nuclides in the field of medicine. The journal promotes the exchange of ideas and information and research in nuclear medicine and includes the medical application of radionuclides and related subjects. It presents original articles, short communications, reviews and letters to the editor.
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