Introduction: Potassium bromate (KBrO 3 ) is an oxidizing agent that is widely used as a flour improver. However, it induces genotoxic and carcinogenic effects on different body organs in a dose and duration-dependent manner.
Aim of this Study:To explore the effects of KBrO 3 on the structure of the rat jejunal mucosa and investigate the potential role of lycopene, a strong antioxidant molecule, in preventing or ameliorating the effect of KBrO 3 . Materials and Methods: Twenty-four adult male albino rats were used and divided equally into four experimental groups; control group, lycopene group that received 10mg of lycopene/kg/day/orally; KBrO 3 group that received 100mg of KBrO 3 /kg/ day/ orally and KBrO 3 and lycopene group that received KBrO 3 and lycopene in the same doses as in the previous groups. Animals were sacrificed after 4 weeks and the specimens from the jejunum were processed for histological, immunohistochemical, and ultrastructural examinations.
Results:The jejunal mucosa of the KBrO 3 treated group showed short and broad villi, discontinuity and desquamation of their lining epithelial cells, inflammatory cellular infiltration, and dilatation of the blood vessels. Moreover, there was a significant decrease in the number of goblet cells and PCNA immuno-stained nuclei in the jejunum. Ultramicroscopic examination showed swollen vacuolated mitochondria, dilated rough endoplasmic reticulum, and shrunken dark nuclei. Interestingly, the group treated with both lycopene and KBrO 3 showed less cytoplasmic vacuolation and mitochondrial abnormalities in the epithelial cells lining the villi. Furthermore, there was a significant improvement in the height of jejunal villi, the number of goblet cells, and PCNA immuno-stained nuclei. Conclusion: KBrO 3 induced cellular damage in the rat jejunal mucosa which was prevented by coadministration of lycopene.