Investigation of the in vitro toxicological properties of the synthetic cannabimimetic drug CP-47,497-C8

Toxicol Appl Pharmacol. 2014 Jun 1;277(2):164-71. doi: 10.1016/j.taap.2014.03.014. Epub 2014 Mar 28.

Abstract

Cannabicyclohexanol (CP-47,497-C8) is a representative of a group of cannabimimetic cyclohexylphenols which is added to herbal mixtures as a cannabis substitute since 2008. Although in the beginning CP-47,497-C8 was the main ingredient of "Spice" and similar products, it was partly replaced by aminoalkylindole-type cannabinoid receptor agonists like JWH-018, JWH-073 or JWH-250, but never completely disappeared from the market. Since information on its toxicological properties is scarce, we investigated the effects of the drug in human derived cell lines. The cytotoxic effects were studied in a panel of assays (SRB, XTT, LDHe and NR tests) in a buccal derived (TR146) and a liver derived (HepG2) cell line. The strongest effects were seen in the two former assays at levels ≥ 7.5 μM indicating that the compound interferes with protein synthesis and causes membrane damage. In additional comet assays, DNA damage was detected at levels ≥10 μM. Experiments with lesion specific enzymes showed that these effects are not due to oxidative damage of DNA bases. The negative findings obtained in Salmonella/microsome assays and the positive results of micronucleus tests with the cell lines indicate that the compound does not cause gene mutations but acts on the chromosomal level. In contrast to other synthetic cannabinoids, no indication for estrogenic/antiestrogenic properties was seen in a luciferase assay with bone marrow derived U2-OS cells. In conclusion, our findings show that the drug has only weak cytotoxic properties. However, the induction of chromosomal damage indicates that it may cause adverse effects in users due to its impact on the stability of the genetic material.

Keywords: CP-47,497-C8; Comet assay; Cytokinesis-block micronucleus (CBMN) cytome assay; Cytotoxicity; Genotoxicity; Synthetic cannabinoid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cannabinoids / toxicity*
  • Cell Membrane / drug effects
  • Cell Membrane / pathology
  • Cell Survival / drug effects
  • Comet Assay
  • Cyclohexanols / toxicity*
  • DNA Damage
  • Dose-Response Relationship, Drug
  • Genes, Reporter
  • Hep G2 Cells
  • Humans
  • Liver / drug effects
  • Liver / metabolism
  • Liver / pathology
  • Micronuclei, Chromosome-Defective / chemically induced
  • Micronucleus Tests
  • Mouth Mucosa / drug effects
  • Mouth Mucosa / metabolism
  • Mouth Mucosa / pathology
  • Mutation
  • Protein Biosynthesis / drug effects
  • Receptors, Estrogen / drug effects
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism
  • Risk Assessment
  • Salmonella typhimurium / drug effects
  • Salmonella typhimurium / genetics
  • Transfection

Substances

  • Cannabinoids
  • Cyclohexanols
  • Receptors, Estrogen
  • CP 47497