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

RMT de Lima, AC Dos Reis… - Biomedicine & …, 2019 - Elsevier
RMT de Lima, AC Dos Reis, JV de Oliveira Santos, JR de Oliveira Ferreira, AL Braga…
Biomedicine & Pharmacotherapy, 2019Elsevier
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 …
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.
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