Cargando…
An Experimental Study on (131)I-CHIBA-1001: A Radioligand for α7 Nicotinic Acetylcholine Receptors
OBJECTIVE: The α7 nicotinic acetylcholine receptors (nAChRs) play a vital role in the pathophysiology of neuropsychiatric diseases such as Alzheimer’s disease and depression. However, there is currently no suitable positron emission tomography (PET) or Single-Photon Emission Computed Tomography (SPE...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728097/ https://www.ncbi.nlm.nih.gov/pubmed/23936161 http://dx.doi.org/10.1371/journal.pone.0070188 |
_version_ | 1782278805090467840 |
---|---|
author | Yin, Lei Zhao, Qian Li, Ling Zhang, Su Lei Chen, Xue Qi Ma, Chao Kang, Lei Liu, Meng Zhang, Chun Li Yan, Ping Wang, Rong Fu |
author_facet | Yin, Lei Zhao, Qian Li, Ling Zhang, Su Lei Chen, Xue Qi Ma, Chao Kang, Lei Liu, Meng Zhang, Chun Li Yan, Ping Wang, Rong Fu |
author_sort | Yin, Lei |
collection | PubMed |
description | OBJECTIVE: The α7 nicotinic acetylcholine receptors (nAChRs) play a vital role in the pathophysiology of neuropsychiatric diseases such as Alzheimer’s disease and depression. However, there is currently no suitable positron emission tomography (PET) or Single-Photon Emission Computed Tomography (SPECT) radioligands for imaging α7 nAChRs in brain. Here our aim is to radiosynthesize a novel SPECT radioligand (131)I-CHIBA-1001 for whole body biodistribution study and in vivo imaging of α7 nAChRs in brain. METHOD: (131)I-CHIBA-1001 was radiosynthesized by chloramine-T method. Different conditions of reaction time and temperature were tested to get a better radiolabeling yield. Radiolabeling yield and radiochemical purities of (131)I-CHIBA-1001 were analyzed by thin layer chromatography (TLC) and high-performance liquid chromatography (HPLC) system. Whole body biodistribution study was performed at different time points post injection of (131)I-CHIBA-1001 in KM mice. Monkey subject was used for in vivo SPECT imaging in brain. RESULT: The radiolabeling yield of (131)I-CHIBA-1001 reached 96% within 1.5∼2.0 h at 90∼95°C. The radiochemical purity reached more than 99% after HPLC purification. (131)I-CHIBA-1001 was highly stable in saline and fresh human serum in room temperature and 37°C separately. The biodistribution data of brain at 15, 30, and 60 min were 11.05±1.04%ID/g, 8.8±0.04%ID/g and 6.28±1.13%ID/g, respectively. In experimental SPECT imaging, the distribution of radioactivity in the brain regions was paralleled with the distribution of α7 nAChRs in the monkey brain. Moreover, in the blocking SPECT imaging study, the selective α7 nAChR agonist SSR180711 blocked the radioactive uptake in the brain successfully. CONCLUSION: The CHIBA-1001 can be successfully radiolabeled with (131)I using the chloramine-T method.( 131)I-CHIBA-1001 can successfully accumulate in the monkey brain and image the α7 acetylcholine receptors. (131)I-CHIBA-1001 can be a candidate for imagingα7 acetylcholine receptors, which will be of great value for the diagnosis and treatment of mental diseases. |
format | Online Article Text |
id | pubmed-3728097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37280972013-08-09 An Experimental Study on (131)I-CHIBA-1001: A Radioligand for α7 Nicotinic Acetylcholine Receptors Yin, Lei Zhao, Qian Li, Ling Zhang, Su Lei Chen, Xue Qi Ma, Chao Kang, Lei Liu, Meng Zhang, Chun Li Yan, Ping Wang, Rong Fu PLoS One Research Article OBJECTIVE: The α7 nicotinic acetylcholine receptors (nAChRs) play a vital role in the pathophysiology of neuropsychiatric diseases such as Alzheimer’s disease and depression. However, there is currently no suitable positron emission tomography (PET) or Single-Photon Emission Computed Tomography (SPECT) radioligands for imaging α7 nAChRs in brain. Here our aim is to radiosynthesize a novel SPECT radioligand (131)I-CHIBA-1001 for whole body biodistribution study and in vivo imaging of α7 nAChRs in brain. METHOD: (131)I-CHIBA-1001 was radiosynthesized by chloramine-T method. Different conditions of reaction time and temperature were tested to get a better radiolabeling yield. Radiolabeling yield and radiochemical purities of (131)I-CHIBA-1001 were analyzed by thin layer chromatography (TLC) and high-performance liquid chromatography (HPLC) system. Whole body biodistribution study was performed at different time points post injection of (131)I-CHIBA-1001 in KM mice. Monkey subject was used for in vivo SPECT imaging in brain. RESULT: The radiolabeling yield of (131)I-CHIBA-1001 reached 96% within 1.5∼2.0 h at 90∼95°C. The radiochemical purity reached more than 99% after HPLC purification. (131)I-CHIBA-1001 was highly stable in saline and fresh human serum in room temperature and 37°C separately. The biodistribution data of brain at 15, 30, and 60 min were 11.05±1.04%ID/g, 8.8±0.04%ID/g and 6.28±1.13%ID/g, respectively. In experimental SPECT imaging, the distribution of radioactivity in the brain regions was paralleled with the distribution of α7 nAChRs in the monkey brain. Moreover, in the blocking SPECT imaging study, the selective α7 nAChR agonist SSR180711 blocked the radioactive uptake in the brain successfully. CONCLUSION: The CHIBA-1001 can be successfully radiolabeled with (131)I using the chloramine-T method.( 131)I-CHIBA-1001 can successfully accumulate in the monkey brain and image the α7 acetylcholine receptors. (131)I-CHIBA-1001 can be a candidate for imagingα7 acetylcholine receptors, which will be of great value for the diagnosis and treatment of mental diseases. Public Library of Science 2013-07-30 /pmc/articles/PMC3728097/ /pubmed/23936161 http://dx.doi.org/10.1371/journal.pone.0070188 Text en © 2013 Yin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Yin, Lei Zhao, Qian Li, Ling Zhang, Su Lei Chen, Xue Qi Ma, Chao Kang, Lei Liu, Meng Zhang, Chun Li Yan, Ping Wang, Rong Fu An Experimental Study on (131)I-CHIBA-1001: A Radioligand for α7 Nicotinic Acetylcholine Receptors |
title | An Experimental Study on (131)I-CHIBA-1001: A Radioligand for α7 Nicotinic Acetylcholine Receptors |
title_full | An Experimental Study on (131)I-CHIBA-1001: A Radioligand for α7 Nicotinic Acetylcholine Receptors |
title_fullStr | An Experimental Study on (131)I-CHIBA-1001: A Radioligand for α7 Nicotinic Acetylcholine Receptors |
title_full_unstemmed | An Experimental Study on (131)I-CHIBA-1001: A Radioligand for α7 Nicotinic Acetylcholine Receptors |
title_short | An Experimental Study on (131)I-CHIBA-1001: A Radioligand for α7 Nicotinic Acetylcholine Receptors |
title_sort | experimental study on (131)i-chiba-1001: a radioligand for α7 nicotinic acetylcholine receptors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728097/ https://www.ncbi.nlm.nih.gov/pubmed/23936161 http://dx.doi.org/10.1371/journal.pone.0070188 |
work_keys_str_mv | AT yinlei anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT zhaoqian anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT liling anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT zhangsulei anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT chenxueqi anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT machao anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT kanglei anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT liumeng anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT zhangchunli anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT yanping anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT wangrongfu anexperimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT yinlei experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT zhaoqian experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT liling experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT zhangsulei experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT chenxueqi experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT machao experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT kanglei experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT liumeng experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT zhangchunli experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT yanping experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors AT wangrongfu experimentalstudyon131ichiba1001aradioligandfora7nicotinicacetylcholinereceptors |