Evaluation of oxidative stress responses and primary DNA damage in blood and brain of rats exposed to low levels of tembotrione. (August 2020)

• Record Type: Journal Article
• Authors: Tariba Lovaković, Blanka; Kašuba, Vilena; Katić, Anja; Kopjar, Nevenka; Marjanović Čermak, Ana Marija; Micek, Vedran; Milić, Mirta; Pavičić, Ivan; Pizent, Alica; Žunec, Suzana; Želježić, Davor
• Is Part Of: Chemosphere. Volume 253(2020)
• Publication Date: 2020-08
• Subjects: Tembotrione -- Comet assay -- Antioxidant enzymes -- Lipid peroxidation; Pollution -- Periodicals; Pollution -- Physiological effect -- Periodicals; Environmental sciences -- Periodicals; Atmospheric chemistry -- Periodicals; 551.511
• DOI: 10.1016/j.chemosphere.2020.126643
• Languages: English
• ISSNs: 0045-6535

Abstract

Abstract: Tembotrione is a rather novel pesticide, usually used for post-emergence weed control. Even though its use is rapidly growing, it is not followed by an adequate flow of scientific evidence regarding its toxicity towards non-target organisms. We evaluated the potential of low doses of tembotrione to induce oxidative stress and cytogenetic damage in blood and brain cells of adult male Wistar rats. Parameters of lipid peroxidation, glutathione levels, activities of antioxidant enzymes and primary DNA damage were assessed following 28-day repeated oral exposure to doses comparable with the currently proposed health-based reference values. The results of the alkaline comet assay showed that such low doses of tembotrione have the potency to inflict primary DNA damage in both peripheral blood leukocytes and brain of treated rats, even with only slight changes in the oxidative biomarker levels. The DNA damage in blood and brain cells of Wistar rats significantly increased at all applied doses, suggesting that tembotrione genotoxicity is mainly a result of direct interaction with DNA while the induction of oxidative stress responses contributes to DNA instability in a lesser extent. The findings of the present study call for further research using other sensitive biomarkers of effect and different exposure scenarios. Graphical abstract: Image 1 Highlights: Male rats were orally exposed to low doses of tembotrione for 28 days. Biochemical and enzyme activity-based endpoints were slightly changed by the treatment. Tembotrione had the potency to inflict DNA damage in leukocytes and in brain cells. Brain cells had higher level of primary DNA damage than leukocytes.