Cytogenetic damage analysis in mice chronically exposed to low-dose internal tritium beta-particle radiation

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Roch-Lefevre, Sandrine | Gregoire, Eric | Martin-Bodiot, C. | Flegal, M. | Fréneau, A. | Blimkie, M. | Bannister, L. | Wyatt, H. | Barquinero, J.-F. | Roy, Laurence | Benadjaoud, Mohamed‐amine | Priest, N. | Jourdain, Jean Rene | Klokov, D.

Edité par CCSD ; Impact journals -

International audience. The aim of this study was to carry out a comprehensive examination of potential genotoxic effects of low doses of tritium delivered chronically to mice and to compare these effects to the ones resulting from equivalent doses of gamma-irradiation. Mice were chronically exposed for one or eight months to either tritiated water (HTO) or organically bound tritium (OBT) in drinking water at concentrations of 10 kBq/L, 1 MBq/L or 20 MBq/L. Dose rates of internal β-particle resulting from such tritium treatments were calculated and matching external gamma-exposures were carried out. We measured cytogenetic damage in bone marrow and in peripheral blood lymphocytes (PBLs) and the cumulative tritium doses (0.009 - 181 mGy) were used to evaluate the dose-response of OBT in PBLs, as well as its relative biological effectiveness (RBE). Neither tritium, nor gamma exposures produced genotoxic effects in bone marrow. However, significant increases in chromosome damage rates in PBLs were found as a result of chronic OBT exposures at 1 and 20 M Bq/L, but not at 10 kBq/L. When compared to an external acute gamma-exposure ex vivo, the RBE of OBT for chromosome aberrations induction was evaluated to be significantly higher than 1 at cumulative tritium doses below 10 mGy. Although found non-existent at 10 kBq/L (the WHO limit), the genotoxic potential of low doses of tritium ( > 10 kBq/L), mainly OBT, may be higher than currently assumed. © Roch-Lefèvre et al.

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