Assessment of the genotoxic/clastogenic potential of coumarin derivative 6,7-dihydroxycoumarin (aesculetin) in multiple mouse organs

Toxicology Reports

Eduardo de Souza Marques¹  Edson Luis Maistro¹  Daiane Bernardoni Salles² 

[1]Programa de Pós-Graduação em Biologia Geral e Aplicada, Universidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatu, SP, Brazil

[2]Universidade Estadual Paulista – UNESP – Faculdade de Filosofia e Ciências, Departamento de Fonoaudiologia, Marília, SP 17525-900, Brazil

关键词: Coumarin derivative;    Aesculetin;    6,7-Dihydroxycoumarin;    Antigenotoxic effects;    Comet assay;    Micronucleus test;   

DOI  :  10.1016/j.toxrep.2015.01.005

来源: DOAJ

【 摘 要 】

6,7-Dihydroxycoumarin (6,7-HC) (aesculetin) is a natural and synthetic coumarin derivative of great interest for use by humans due to their potent antioxidant properties. Considering that there are no reports that assess the in vivo genetic toxicity of 6,7-HC, the aim of the present study was to investigate its genotoxic potential in terms of DNA damage in peripheral blood, liver, bone marrow and testicular cells of Swiss albino mice by the comet assay, and its clastogenic/aneugenic potential in bone marrow cells using the micronucleus test. In addition, the ability of 6,7-HC to modulate the genotoxic effects induced by doxorubicin (DXR) was also preliminarily evaluated. Cytotoxicity was assessed by scoring polychromatic (PCE) and normochromatic (NCE) erythrocytes’ ratio. The test compound was administered orally at doses of 25, 50 and 500 mg kg−1 isolated and also simultaneously to DXR (80 mg kg−1). The results showed that 6,7-HC did not induce significant DNA damage in any of the analyzed cells, and also did not show any significant increase in micronucleated PCE at the three tested doses. The PCE/NCE ratio indicated no cytotoxicity. Moreover, the extent of DNA damage induced by DXR decreased significantly only in peripheral blood and testicular cells, and only at the lowest dose of 6,7-HC.

【 授权许可】

Unknown