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Tumorigenicity study of disodium glycyrrhizinate administered orally to mice

Insights

Long-term oral administration of Disodium glycyrrhizinate (DG) to mice showed no evidence of chronic toxicity or tumorigenicity. Studies found no significant differences in tumor incidence or type between DG-treated and control groups.

Area of Science:

  • Toxicology
  • Pharmacology
  • Carcinogenesis

Background:

  • Disodium glycyrrhizinate (DG) is derived from licorice root.
  • Assessing the long-term safety and potential carcinogenicity of DG is crucial for its therapeutic applications.

Purpose of the Study:

  • To evaluate the chronic toxicity and tumorigenicity of Disodium glycyrrhizinate (DG) in mice following long-term oral administration.

Main Methods:

  • Male and female B6C3F1 mice were administered varying concentrations of DG in drinking water for 96 weeks.
  • Dose levels included maximum tolerated doses and lower concentrations, with control groups receiving no DG.
  • Tumor incidence, latency, and type distribution were monitored until study termination at 110 weeks.

Main Results:

  • No significant differences were observed in tumor incidence between DG-treated groups and control groups.
  • The latent period for tumor development and the distribution of tumor types were comparable across all experimental groups.
  • No evidence of chronic toxicity or tumorigenicity was detected in mice exposed to DG.

Conclusions:

  • Long-term oral administration of Disodium glycyrrhizinate (DG) did not induce chronic toxicity or tumorigenicity in mice.
  • The findings suggest that DG is safe for long-term use at the tested concentrations.
  • Further research may explore specific mechanisms of DG's safety profile.

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