Cannabidiol and Tetrahydrocannabinol Antinociceptive Activity is Mediated by Distinct Receptors in Caenorhabditis elegans

Neurochem Res. 2024 Apr;49(4):935-948. doi: 10.1007/s11064-023-04069-6. Epub 2023 Dec 23.

Abstract

Cannabis has gained popularity in recent years as a substitute treatment for pain following the risks of typical treatments uncovered by the opioid crisis. The active ingredients frequently associated with pain-relieving effects are the phytocannabinoids Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD), but their effectiveness and mechanisms of action are still under research. In this study, we used Caenorhabditis elegans, an ideal model organism for the study of nociception that expresses mammal ortholog cannabinoid (NPR-19 and NPR-32) and vanilloid (OSM-9 and OCR-2) receptors. Here, we evaluated the antinociceptive activity of THC and CBD, identifying receptor targets and several metabolic pathways activated following exposure to these molecules. The thermal avoidance index was used to phenotype each tested C. elegans experimental group. The data revealed for the first time that THC and CBD decreases the nocifensive response of C. elegans to noxious heat (32-35 °C). The effect was reversed 6 h post- CBD exposure but not for THC. Further investigations using specific mutants revealed CBD and THC are targeting different systems, namely the vanilloid and cannabinoid systems, respectively. Proteomic analysis revealed differences following Reactome pathways and gene ontology biological process database enrichment analyses between CBD or THC-treated nematodes and provided insights into potential targets for future drug development.

Keywords: Caenorhabditis elegans; Cannabis sativa; Cannabidiol; Nociception; Pain; Phytocannabinoid; Proteomics; Tetrahydrocannabinol; Vanilloid receptor.

MeSH terms

  • Analgesics / pharmacology
  • Animals
  • Caenorhabditis elegans
  • Caenorhabditis elegans Proteins*
  • Cannabidiol* / pharmacology
  • Cannabinoids*
  • Dronabinol / pharmacology
  • Humans
  • Mammals
  • Pain
  • Proteomics
  • Receptors, G-Protein-Coupled

Substances

  • Cannabidiol
  • Dronabinol
  • Cannabinoids
  • Analgesics
  • NPR-32 protein, C elegans
  • Caenorhabditis elegans Proteins
  • Receptors, G-Protein-Coupled
  • NPR-19 protein, C elegans