Toxic, cytogenetic and antitumor evaluations of [6]-gingerol in non-clinical in vitro studies

Biomed Pharmacother. 2019 Jul:115:108873. doi: 10.1016/j.biopha.2019.108873. Epub 2019 Apr 16.

Abstract

Gingerol - [6]-gingerol ((S)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-decanone; [6]-G) - is a phenolic compound with several pharmacological properties. Herein, the aim of the study was to evaluate the toxicogenic effects of [6]-G on Artemia salina nauplii, Allium cepa, HL-60 cell line and Sarcoma 180 (S-180) ascitic fluid cells.For toxic and genotoxic analysis, it was used [6]-G concentrations of 5, 10, 20 and 40 μg mL-1. For cytotoxic evaluation using the MTT test (3- [4,5-dimethyl-thiazol-2-yl] -2,5-diphenyl tetrazolium bromide), serial [6]-G dilutions (1.56-100 μg mL-1) were performed, and S-180, HL-60 and peripheral blood mononuclear cells (PBMC) were treated for 72 h. The IC50 of [6]-G were 1.14, 5.73 and 11.18 μg mL-1 for HL-60, S-180 and PBMC, respectively, indicating a possible selectivity against tumor cell lines. At higher concentrations (>10 μg mL-1), toxicity and genotoxicity were observed in the A. cepa test, especially at 40 μg mL-1. Mechanisms indicating apoptosis, such as toxicity, cytotoxicity and nuclear abnormalities (bridges, fragments, delays, loose chromosomes and micronuclei) suggest that [6]-G has potential for antitumor pharmaceutical formulations.

Keywords: Antitumor activity; Toxicogenic; [6]-Gingerol.

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Artemia / drug effects
  • Biological Assay*
  • Catechols / administration & dosage
  • Catechols / pharmacology*
  • Cell Line, Tumor
  • Cell Survival / drug effects*
  • Dose-Response Relationship, Drug
  • Fatty Alcohols / administration & dosage
  • Fatty Alcohols / pharmacology*
  • Humans
  • Mice
  • Onions / cytology

Substances

  • Antineoplastic Agents, Phytogenic
  • Catechols
  • Fatty Alcohols
  • gingerol