Department of Chemistry, School of Physical & Decision Sciences (SPDS), Babasaheb Bhimrao Ambedkar University (A Central University), Lucknow 226025, UP, India; Division of Cyclotron and Radiopharmaceutical Sciences, Institute of Nuclear Medicine and Allied Sciences, Brig. S. K. Mazumdar Road, Delhi 110054, India; Department of Chemistry, University of Delhi, Delhi 110054, India.
Division of Cyclotron and Radiopharmaceutical Sciences, Institute of Nuclear Medicine and Allied Sciences, Brig. S. K. Mazumdar Road, Delhi 110054, India.
Bioorg Chem. 2021 Jun;111:104972. doi: 10.1016/j.bioorg.2021.104972. Epub 2021 May 13.
Quantitative changes in expression level of 5HT are somewhere related to common neurological disorders such as anxiety, major depression and schizophrenia. We have designed EDTA conjugated SPECT imaging probe for localization of 5HT receptor in brain. For designing SPECT probe we have employed the concept of bivalent approach and a homodimeric system with desirable pharmacokinetics of 5HT imaging. Tc-EDHT was also evaluated for its stability through serum stability assay and glutathione challenge experiment. Biodistribution study showed the highest accumulation of radioactivity in kidney which depicted the renal mode of excretion from the body. However in brain the uptake of 1.21% ID per gram was observed in initial 5 min of drug administration. On blocking the receptor this percent get decreased to 0.97% ID per gram. The regional distribution in brain was also performed which showed the accumulation of drug in cerebellum, cortex and hippocampus part, which are already known for 5HT expression. Dynamic study in rabbit is also in support of results derived from biodistribution and blood kinetics experiment. These finding suggest that Tc-EDHT holds promising place for further optimization before nuclear medicine applications in different animal species.
5HT 表达水平的定量变化与常见的神经紊乱有关,如焦虑、重度抑郁症和精神分裂症。我们设计了 EDTA 缀合的 SPECT 成像探针,用于定位大脑中的 5HT 受体。为了设计 SPECT 探针,我们采用了双价方法的概念和具有理想 5HT 成像药代动力学的同二聚体系统。还通过血清稳定性测定和谷胱甘肽挑战实验评估了 Tc-EDHT 的稳定性。生物分布研究表明,放射性在肾脏中的积累最高,这表明药物从体内以肾脏排泄的方式排出。然而,在大脑中,在给予药物的最初 5 分钟内观察到每克 1.21%ID 的摄取。在阻断受体后,这一百分比下降到每克 0.97%ID。还对大脑进行了区域分布研究,结果显示药物在小脑、皮质和海马部分积累,这些部位已经被认为是 5HT 表达的部位。兔的动态研究也支持从生物分布和血液动力学实验中得出的结果。这些发现表明,Tc-EDHT 在进一步优化之前,有望在不同动物物种的核医学应用中发挥作用。