Author/Authors :
Carranza-Rosales, Pilar Departamento de Biología Celular y Molecular - Centro de Investigación Biomédica del Noreste - Instituto Mexicano del Seguro Social - Monterrey, NL. México , Carranza-Torres, Irma Edith Departamento de Biología Celular y Molecular - Centro de Investigación Biomédica del Noreste - Instituto Mexicano del Seguro Social - Monterrey, NL. México , Morán-Martínez, Javier Departamento de Biología Celular y Ultraestructura - Centro de Investigación Biomédica - Facultad de Medicina - Universidad Autónoma de Coahuila - Torreón, Coah. México , Betancourt-Martínez, Nadia Denys Departamento de Biología Celular y Ultraestructura - Centro de Investigación Biomédica - Facultad de Medicina - Universidad Autónoma de Coahuila - Torreón, Coah. México , Viveros-Valdez, Ezequiel Departamento de Química Analítica - Facultad de Ciencias Biológicas - Universidad Autónoma de Nuevo León - San Nicolás de los Garza, NL. México , García-Davis, Sara Departamento de Química Analítica - Facultad de Ciencias Biológicas - Universidad Autónoma de Nuevo León - San Nicolás de los Garza, NL. México , Guzmán-Delgado, Nancy Elena División de Investigación - Unidad Médica de Alta Especialidad # 34 - Instituto Mexicano del Seguro Social - Monterrey, NL. México , Balderas- Rentería, Isaías Laboratorio de Ingeniería Genética y Genómica - Facultad de Ciencias Químicas - Universidad Autónoma de Nuevo León - San Nicolás de los Garza, NL. México
Abstract :
Precision-cut tissue slices are considered an organotypic 3D model widely used in
biomedical research. The comet assay is an important screening test for early genotoxicity risk
assessment that is mainly applied on in vitro models. The aim of the present study was to provide a
3D organ system for determination of genotoxicity using a modified method of the comet assay since
the stromal components from the original tissue make this technique complicated.
Materials and Methods: A modified comet assay technique was validated using precision-cut hamster
kidney slices to analyze the antigenotoxic effect of the phenolic compounds caffeic acid, chlorogenic
acid, and rosmarinic acid in tissue slices incubated with 15 μM HgCl2. Cytotoxicity of the phenolic
compounds was studied in Vero cells, and by morphologic analysis in tissue slices co-incubated with
HgCl2 and phenolic compounds.
Results: A modification of the comet assay allows obtaining better and clear comet profiles for
analysis. Non-cytotoxic concentrations of phenolic acids protected kidney tissue slices against
mercury-induced DNA damage, and at the same time, were not nephrotoxic. The highest protection
was provided by 3 μg/ml caffeic acid, although 6 μg/ml rosmarinic and 9 μg/ml chlorogenic acids also
exhibited protective effects.
Conclusion: This is the first time that a modification of the comet assay technique is reported as a tool
to visualize the comets from kidney tissue slices in a clear and simple way. The phenolic compounds
tested in this study provided protection against mercury-induced genotoxic damage in precision-cut
kidney slices.
Keywords :
Comet assay , Genotoxicity , Mercuric chloride , Phenolic compounds , Precision-cut tissue slices