Journal
CANNABIS AND CANNABINOID RESEARCH
Volume 6, Issue 6, Pages 522-527Publisher
MARY ANN LIEBERT, INC
DOI: 10.1089/can.2020.0103
Keywords
cannabidiol; toxicity; lifespan; motility; aging; health
Categories
Funding
- Canopy Growth Corporation
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The study found that cannabidiol (CBD) showed no significant acute or long-term toxicity in Caenorhabditis elegans at physiologically relevant concentrations. Notably, 40 micromolar CBD significantly increased heat stress resistance and led to the highest life extension and late-stage activity increase.
Introduction: Despite widespread use of cannabidiol (CBD), no lifelong toxicity study has been published to date. Caenorhabditis elegans is often used in preclinical lifelong toxicity studies, due to an estimated 60-80% of their genes having a human ortholog, and their short lifespan of similar to 2-3 weeks. In this study, we examined both acute and long-term exposure studies of CBD at physiologically relevant concentrations. Materials and Methods: Acute toxicity was determined by treating day 1 adults with a wide range of CBD concentrations (0.4 mu M to 4mM) and assessing mortality and motility compared to control animals. Thermotolerance was examined by treating adult animals with CBD (0.4 mu M to 4mM) and exposing themto 37 degrees C for 4 h, and then scoring for the number of alive animals treated with CBD compared to controls. Long-term toxicity was assessed by exposing day 1 adults to 10, 40, and 100 mu M CBD until all animals perished. Control animals had no active drug exposure. Results: We report both acute and long-term exposure studies of CBD to adult C. elegans at physiologically relevant concentrations. Acute toxicity results showed that no animal died when exposed to 0.4-4000 mu M CBD. The thermotolerance study showed that 40 mu M CBD, but not other treatment levels, significantly increased resistance to heat stress by 141% compared to the untreated controls. Notably, whole-life exposure of C. elegans to 10-100 mu M CBD revealed a maximum life extension of 18% observed at 40 mu M CBD. In addition, motility analysis of the same groups revealed an increase in late-stage life activity by up to 206% compared to controls. Conclusion: These results serve as the only CBD lifelong exposure data in an in vivo model to date. While further research into the lifelong use of CBD should be carried out in mammalian models, the C. elegans model indicates a lack of long-term toxicity at physiologically relevant concentrations.
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