The Anti-Inflammatory Effects of Cannabis sativa Extracts on LPS-Induced Cytokines Release in Human Macrophages

Molecules. 2023 Jun 25;28(13):4991. doi: 10.3390/molecules28134991.

Abstract

Inflammation is the response of the innate immune system to any type of injury. Although acute inflammation is critical for survival, dysregulation of the innate immune response leads to chronic inflammation. Many synthetic anti-inflammatory drugs have side effects, and thus, natural anti-inflammatory compounds are still needed. Cannabis sativa L. may provide a good source of anti-inflammatory molecules. Here, we tested the anti-inflammatory properties of cannabis extracts and pure cannabinoids in lipopolysaccharide (LPS)-induced inflammation in human THP-1 macrophages. We found that pre-treatment with cannabidiol (CBD), delta-9-tetrahydrocannabinol (THC), or extracts containing high levels of CBD or THC reduced the level of induction of various cytokines. The CBD was more efficient than THC, and the extracts were more efficient than pure cannabinoids. Finally, IL-6, IL-10, and MCP-1 cytokines were most sensitive to pre-treatments with CBD and THC, while IL-1β, IL-8, and TNF-α were less responsive. Thus, our work demonstrates the potential of the use of cannabinoids or/and cannabis extracts for the reduction of inflammation and establishes IL-6 and MCP-1 as the sensitive markers for the analysis of the effect of cannabinoids on inflammation in macrophages.

Keywords: cannabidiol; cannabis; inflammation; lipopolysaccharide; macrophages; tetrahydrocannabinol.

MeSH terms

  • Anti-Inflammatory Agents / pharmacology
  • Cannabidiol* / analysis
  • Cannabinoid Receptor Agonists
  • Cannabinoids* / pharmacology
  • Cannabinoids* / therapeutic use
  • Cannabis*
  • Cytokines
  • Hallucinogens*
  • Humans
  • Inflammation / chemically induced
  • Inflammation / drug therapy
  • Interleukin-6
  • Lipopolysaccharides / toxicity
  • Macrophages
  • Plant Extracts / pharmacology

Substances

  • Anti-Inflammatory Agents
  • Cannabidiol
  • Cannabinoid Receptor Agonists
  • Cannabinoids
  • Cytokines
  • Hallucinogens
  • Interleukin-6
  • Lipopolysaccharides
  • Plant Extracts

Grants and funding

This research was funded by MITACS grants IT11447 and IT15089.