The carotenoid lycopene protects rats against DNA damage induced by Ochratoxin A

• Published in: Toxicon (Oxford) 2013-10, Vol.73, p.96-103
• Main Authors: Aydin, Sevtap, Palabiyik, Şaziye Sezin, Erkekoglu, Pinar, Sahin, Gonul, Başaran, Nurşen, Giray, Belma Kocer
• Format: Article
• Language: English
• Subjects: Analysis of Variance; Animals; Carotenoids; Carotenoids - pharmacology; Comet Assay; Damage; Deoxyribonucleic acid; DNA damage; DNA Damage - drug effects; Genotoxicity; hepatocytes; hepatotoxicity; Kidneys; Lycopene; Lymphocytes; Male; Mutagenicity Tests; Mycotoxins; nephrotoxicity; Ochratoxin A; Ochratoxins - toxicity; Oxidative stress; Protective; protective effect; Rats; Rats, Sprague-Dawley; Scavenging; singlet oxygen; tail; Tail - pathology; Time Factors; tissues
• ISSN: 0041-0101; 1879-3150
• DOI: 10.1016/j.toxicon.2013.07.004

Ochratoxin A (OTA), one of the most prevalent mycotoxins in the world, has nephrotoxic and hepatotoxic properties. Lycopene is an important carotenoid and has a high singlet-oxygen and free-radical scavenging capacity. This study was designed to investigate the possible protective effects of lycopene against the genotoxicity of OTA in rat tissues using the alkaline comet assay. Male Sprague–Dawley rats were used in the experiments. OTA (0.5 mg/kg b.w./day) was administered by gavage for 14 days, whereas lycopene was applied on the last 7 days or for 14 days of the feeding period, with OTA treatment. OTA caused marked increases in tail length, tail moment, and tail intensity vs. control both in the kidney and liver cells, but not in the lymphocytes. Lycopene administration alone for 7 and 14 days did not provide any significant change in DNA damage of the lymphocytes, renal and hepatic cells vs. controls. However, lycopene for both 7 and 14 days, with OTA exposure in renal and hepatic cells, supplied significant decreases in tail length, tail moment, and tail intensity vs. OTA-exposed rats. The effect of 14 days supplementation seemed to be more protective, particularly against hepatic cells. These results suggest that lycopene may protect hepatic and renal tissue from OTA-induced DNA damage. •We investigated the effects of lycopene against genotoxicity of Ochratoxin A (OTA) in rat tissues.•Lycopene for 7 and 14 days did not provide marked change in DNA damage of renal and hepatic cells.•OTA caused marked increases in DNA damage vs. control both in the kidney and liver cells.•Lycopene with OTA exposure supplied marked decreases in DNA damage in renal and hepatic cells.•Lycopene for 14 days seemed to be more protective, particularly against hepatic cells.