Zearalenone induces chromosome aberrations in mouse bone marrow: preventive effect of 17β-estradiol, progesterone and Vitamin E

• Published in: Mutation research. Genetic toxicology and environmental mutagenesis Vol. 565; no. 2; pp. 139 - 149
• Main Authors: Ouanes, Z., Ayed-Boussema, I., Baati, T., Creppy, E.E., Bacha, H.
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 03.01.2005; Elsevier
• Subjects: 17β-Estradiol; Biological and medical sciences; Chromosome aberrations; Fundamental and applied biological sciences. Psychology; Genetics of eukaryotes. Biological and molecular evolution; Medical sciences; Progesterone; Toxicology; Vitamin E; Zearalenone; 17β-Est; ZEN; Mit C; Vitamin E; 17β-Estradiol; Zearalenone; Vit E; Progesterone; Prog; Chromosome aberrations; Chromosomal aberration; Estrogen; Rodentia; Vitamin; Ovarian hormone; Vertebrata; Toxicology; Mammalia; Mouse; Bone marrow; Genetics; Sex steroid hormone
• ISSN: 1383-5718; 1879-3592
• DOI: 10.1016/j.mrgentox.2004.10.005

The cytogenetic effect of zearalenone (ZEN), a non-steroidal estrogenic mycotoxin, was evaluated in vivo, in mouse bone marrow cells, by assessing the percentage of cells bearing different chromosome aberrations. The studies included different conditions for animal treatment, as follows: (1) single intraperitoneal (ip) injection, (2) repeated ip injections, (3) pre-treatment for 24 h with Vitamin E (Vit E), and (4) pre-treatment for 4 h with 17β-estradiol (17β-Est) or progesterone (Prog). ZEN induced different types of chromosome aberrations, which was concentration-dependent (2–20 mg/kg bw). These doses corresponded to 0.4–4% of the LD 50 in the mouse. Interestingly, when the dose of ZEN (40 mg/kg) was fractionated into four equivalent doses (4 × 10 mg/kg bw), into three doses (15 + 10 + 15 mg/kg bw), or into two equivalent doses (2 × 20 mg/kg bw), given every 24 h, the percentage of chromosome aberrations increased significantly. This finding suggests that ZEN proceeds by reversible binding on receptors that could become saturated, and that it damages the chromosomes in a ‘hit and go’ manner. Furthermore, pre-treatment of animals with 17β-estradiol or progesterone significantly decreased the percentage of chromosome aberrations, suggesting that (i) these hormones bind to the same cytoplasmic receptors transported into the nucleus to elicit DNA damage, (ii) they may play a role in preventing chromosome aberrations induced by ZEN. Similarly, Vit E prevented these chromosome aberrations indicating that Vit E, previously reported to prevent most of the toxic effects induced by ZEN, may also bind to the same receptors.