4.7 Article

Positron Emission Tomography Imaging of the Endocannabinoid System: Opportunities and Challenges in Radiotracer Development

期刊

JOURNAL OF MEDICINAL CHEMISTRY
卷 64, 期 1, 页码 123-149

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.0c01459

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资金

  1. K. C. Wong Education Foundation
  2. National Natural Science Foundation of China [81701751, 81871383]
  3. Guangdong Basic and Applied Basic Research Foundation [2020A1515011192]
  4. Fundamental Research Funds for the Central Universities [21619104]
  5. Project of Innovative Team for the Guangdong University [2018KCXTD001]
  6. NIH [DA038000, DA043507, AG054473, AG052414, DA033760]
  7. Azrieli Foundation
  8. Canada Foundation for Innovation
  9. Ontario Research Fund
  10. Canada Research Chairs Program
  11. Swiss National Science Foundation [P2EZP3_175137]
  12. Swiss National Science Foundation (SNF) [P2EZP3_175137] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

The endocannabinoid system (ECS) plays a crucial role in various biological functions, including cannabinoid receptors and enzymes responsible for endocannabinoid synthesis and degradation. Significant progress has been made in developing PET tracers targeting different components of the ECS, particularly for neuroimaging applications. The review discusses the development of state-of-the-art PET tracers for the ECS, including their chemical design, pharmacological properties, radiolabeling, and imaging applications.
The endocannabinoid system (ECS) is involved in a wide range of biological functions and comprises cannabinoid receptors and enzymes responsible for endocannabinoid synthesis and degradation. Over the past 2 decades, significant advances toward developing drugs and positron emission tomography (PET) tracers targeting different components of the ECS have been made. Herein, we summarized the recent development of PET tracers for imaging cannabinoid receptors 1 (CB1R) and 2 (CB2R) as well as the key enzymes monoacylglycerol lipase (MAGL) and fatty acid amide hydrolase (FAAH), particularly focusing on PET neuroimaging applications. State-of-the-art PET tracers for the ECS will be reviewed including their chemical design, pharmacological properties, radiolabeling, as well as preclinical and human PET imaging. In addition, this review addresses the current challenges for ECS PET biomarker development and highlights the important role of PET ligands to study disease pathophysiology as well as to facilitate drug discovery.

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