Molecular Targets of Cannabinoids Associated with Depression

Curr Med Chem. 2022;29(11):1827-1850. doi: 10.2174/0929867328666210623144658.

Abstract

Novel therapeutic strategies are needed to address depression, a major neurological disorder affecting hundreds of millions of people worldwide. Cannabinoids and their synthetic derivatives have demonstrated numerous neurological activities and may have the potential to be developed into new treatments for depression. This review highlights cannabinoid (CB) receptors, monoamine oxidase (MAO), N-methyl-D-aspartate (NMDA) receptor, gammaaminobutyric acid (GABA) receptor, and cholecystokinin (CCK) receptor as key molecular targets of cannabinoids that are associated with depression. The anti-depressant activity of cannabinoids and their binding modes with cannabinoid receptors are discussed, providing insights into rational design and discovery of new cannabinoids or cannabimimetic agents with improved druggable properties.

Keywords: CB receptors; CCK receptors; Cannabinoids; GABA receptors; MAO; NMDA receptors; depression; molecular targets.

Publication types

  • Review

MeSH terms

  • Cannabinoids* / pharmacology
  • Cannabinoids* / therapeutic use
  • Depression / drug therapy
  • Humans
  • Monoamine Oxidase / metabolism
  • Receptor, Cannabinoid, CB1 / metabolism
  • Receptors, Cannabinoid / metabolism
  • Receptors, N-Methyl-D-Aspartate

Substances

  • Cannabinoids
  • Receptor, Cannabinoid, CB1
  • Receptors, Cannabinoid
  • Receptors, N-Methyl-D-Aspartate
  • Monoamine Oxidase