Multi-Omics Reveals the Effects of Cannabidiol on Gut Microbiota and Metabolic Phenotypes

Cannabis Cannabinoid Res. 2024 Jun;9(3):714-727. doi: 10.1089/can.2022.0331. Epub 2023 Apr 25.

Abstract

Introduction: Cannabidiol (CBD) has important pharmacological activity, which includes antispasmodic, antioxidant, antithrombotic, and antianxiety properties. CBD has been applied as a health supplement to atherosclerosis. However, CBDs effect on gut microbiota and metabolic phenotype is unclear. Materials and Methods: We constructed a high production of cardiovascular risk factors, such as trimethylamine-N-oxide (TMAO) and phenylacetylglutamine (PAGln), in a mouse model using Clostridium sporogenes colonization. We used 16S ribosomal RNA (rRNA) gene sequencing and ultra-high performance liquid chromatography-quadrupole time-of flight mass spectrometry-based metabolomics to evaluate the effect of CBD on gut microbiota and plasma metabolites. Results: CBD decreased the levels of creatine kinase (CK), alanine transaminase (ALT), and low-density lipoprotein cholesterol and markedly increased high-density lipoprotein cholesterol. Furthermore, CBD treatment increased the abundance of beneficial bacteria, which include Lachnospiraceae_NK4A136 and Blautia in the gut, but it decreased the levels of TMAO and PAGln in the plasma. Conclusion: CBD might have beneficial effects for cardiovascular protection.

Keywords: CBD; cardiovascular protection; gut microbiota; metabolic phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cannabidiol* / pharmacology
  • Gastrointestinal Microbiome* / drug effects
  • Male
  • Metabolomics*
  • Methylamines / blood
  • Methylamines / metabolism
  • Methylamines / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Multiomics
  • Phenotype
  • RNA, Ribosomal, 16S

Substances

  • Cannabidiol
  • trimethyloxamine
  • RNA, Ribosomal, 16S
  • Methylamines