Schröder Susann, Scheunemann Matthias, Wenzel Barbara, Brust Peter
Department of Research and Development, ROTOP Pharmaka Ltd., 01328 Dresden, Germany.
Department of Neuroradiopharmaceuticals, Institute of Radiopharmaceutical Cancer Research, Research Site Leipzig, Helmholtz-Zentrum Dresden-Rossendorf (HZDR), 04318 Leipzig, Germany.
Int J Mol Sci. 2021 Apr 7;22(8):3832. doi: 10.3390/ijms22083832.
Cyclic nucleotide phosphodiesterases (PDEs) represent one of the key targets in the research field of intracellular signaling related to the second messenger molecules cyclic adenosine monophosphate (cAMP) and/or cyclic guanosine monophosphate (cGMP). Hence, non-invasive imaging of this enzyme class by positron emission tomography (PET) using appropriate isoform-selective PDE radioligands is gaining importance. This methodology enables the in vivo diagnosis and staging of numerous diseases associated with altered PDE density or activity in the periphery and the central nervous system as well as the translational evaluation of novel PDE inhibitors as therapeutics. In this follow-up review, we summarize the efforts in the development of novel PDE radioligands and highlight (pre-)clinical insights from PET studies using already known PDE radioligands since 2016.
环核苷酸磷酸二酯酶(PDEs)是细胞内信号传导研究领域中与第二信使分子环磷酸腺苷(cAMP)和/或环磷酸鸟苷(cGMP)相关的关键靶点之一。因此,使用合适的亚型选择性PDE放射性配体通过正电子发射断层扫描(PET)对这类酶进行非侵入性成像正变得越来越重要。这种方法能够对许多与外周和中枢神经系统中PDE密度或活性改变相关的疾病进行体内诊断和分期,以及对新型PDE抑制剂作为治疗药物进行转化评估。在这篇后续综述中,我们总结了新型PDE放射性配体开发方面的工作,并突出了自2016年以来使用已知PDE放射性配体的PET研究的(临床前)见解。