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

Toxicol Appl Pharmacol

Institute of Cancer Research, Department of Internal Medicine 1, Comprehensive Cancer Center, Medical University of Vienna, Borschkegasse 8A, 1090 Vienna, Austria. Electronic address:

Published: June 2014

AI Article Synopsis

  • Cannabicyclohexanol (CP-47,497-C8) is a synthetic cannabinoid used as a cannabis substitute in products like "Spice" since 2008, though it has been largely replaced by other compounds like JWH-018.
  • Researchers studied its effects on human cell lines, finding significant cytotoxicity at high concentrations, which affected protein synthesis and caused membrane damage, alongside DNA damage at levels ≥10 μM.
  • While the compound does not appear to cause gene mutations, it does induce chromosomal damage, suggesting potential adverse effects on genetic stability in users.

Article 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.

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Source
http://dx.doi.org/10.1016/j.taap.2014.03.014DOI Listing

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