Absence of DNA damage in multiple organs (blood, liver, kidney, thyroid gland and urinary bladder) after acute fluoride exposure in rats

Author:

de Lima Leite Aline1,Ferreira Santiago Junior Joel1,Mauad Levy Flavia1,Gutierrez Maria Andrea1,da Silva Fernandes Mileni1,Favero Salvadori Daisy Maria2,Araki Ribeiro Daniel3,Afonso Rabelo Buzalaf Marilia4

Affiliation:

1. Department of Biological Sciences, Bauru Dental School, University of São Paulo, USP, SP, Brazil

2. Department of Pathology, Botucatu Medical School, São Paulo State University, UNESP, SP, Brazil

3. Department of Pathology, Botucatu Medical School, São Paulo State University, UNESP, SP, Brazil, Department of Health Sciences, Federal University of São Paulo, UNIFESP, Santos, SP, Brazil

4. Department of Biological Sciences, Bauru Dental School, University of São Paulo, USP, SP, Brazil,

Abstract

Fluoride has been widely used in dentistry as a caries prophylactic agent. However, there has been some speculation that excess fluoride could cause an impact on genome integrity. In the current study, the potential DNA damage associated with exposure to fluoride was assessed in cells of blood, liver, kidney, thyroid gland and urinary bladder by the single cell gel (comet) assay. Male Wistar rats aging 75 days were distributed into seven groups: Groups 1 (control), 2, 3, 4, 5, 6 and 7 received 0 (deionized water), 10, 20, 40, 60, 80 and 100 mgF/Kg body weight from sodium fluoride (NaF), respectively, by gastrogavage. These groups were killed at 2 h after the administration of the fluoride doses. The level of DNA strand breaks did not increase in all organs evaluated and at all doses of NaF tested, as depicted by the mean tail moment. Taken together, our results suggest that oral exposure to NaF did not result in systemic genotoxic effect in multiple organs related to fluoride toxicity. Since DNA damage is an important step in events leading to carcinogenesis, this study represents a relevant contribution to the correct evaluation of the potential health risk associated with chemical exposure. Human & Experimental Toxicology ( 2007) 26, 435—440

Publisher

SAGE Publications

Subject

Health, Toxicology and Mutagenesis,Toxicology,General Medicine

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