Title:Cytotoxic and Chemopreventive Effects of Gemin D Against Different Mutagens Using In Vitro and In Vivo Assays
VOLUME: 17 ISSUE: 5
Author(s):Cristiene Costa Carneiro*, Aroldo Vieira de Moraes-Filho, Amanda Silva Fernandes, Suzana da Costa Santos, Daniela de Melo e Silva and Lee Chen Chen
Affiliation:Department of Genetics, Institute of Biological Sciences, Federal University of Goias, C.P. 131, Campus Samambaia, P.O.Box 74001-970, Goiania, Institute of Biological Sciences, Federal University of Goias, Goiania, Institute of Biological Sciences, Federal University of Goias, Goiania, Chemistry Institute, Federal University of Goias, Goiania, Institute of Biological Sciences, Federal University of Goias, Goiania, Institute of Biological Sciences, Federal University of Goias, Goiania
Keywords:Ellagitannin, gemin D, cytotoxic and protective effects against different mutagens, ames test, micronucleus test, comet assay.
Abstract:Background: Gemin D (GD) is an ellagitannin found in several plant species rich in phenolic compounds.
Its many beneficial properties include antioxidant and antitumoral.
Objective: The present study assessed the genotoxicity, cytotoxicity, antigenotoxicity, and anticytotoxicity of GD by in
vitro and in vivo assays.
Method: The Ames mutagenicity assay in Salmonella typhimurium, Micronucleus and Comet tests in mice were used
to evaluate the biological activities mentioned above. To assess the GD’s protective effects against DNA damage
induced by different mutagens we performed co-, pre- and/or post-treatment in these assays.
Results: There was no genotoxic effect of GD via Ames and Micronucleus tests, but in the Comet assay the highest
dose induced DNA damage. This same highest dose presented a significant cytotoxicity in mice. In the
antigenotoxicity, GD protected DNA against the action of 4-nitroquinoline-1-oxide and sodium azide by Ames test,
and also against the harmful action of cyclophosphamide in pre- and co-treatment by Micronucleus and Comet tests,
but it did not protect DNA in post-treatment. Regarding to anticytotoxicity, GD provoked an anticytotoxic effect only
during pre-treatment.
Conclusion: Therefore, GD showed relevant antigenotoxic, anticytotoxic and cytotoxic effects, which indicate that it
may be a probable candidate for chemoprevention or for the development of new cancer therapies.
