Bouaziz-Ketata Hanen, Salah Ghada Ben, Mahjoubi Amira, Aidi Zied, Kallel Choumous, Kammoun Hassen, Fakhfakh Faiza, Zeghal Najiba
Animal Physiology Laboratory, UR/11 ES70, Sfax Faculty of Sciences, University of Sfax, 3000, Sfax, Tunisia.
Laboratory of Human Molecular Genetics, Faculty of Medicine, Sfax, 3029, Sfax, Tunisia.
Environ Toxicol. 2015 Nov;30(11):1275-84. doi: 10.1002/tox.21998. Epub 2014 Apr 17.
The present study was carried out to examine the adverse hematotoxic and genotoxic effects of water nitrate pollution on male adult rats and the use of hyparrhenia hirta methanolic extract in alleviating these effects. Sodium nitrate (NaNO3 ) was administered to adult rats by oral gavage at a dose of 400 mg kg(-1) bw daily for 50 days, while hyparrhenia hirta methanolic extract was given by drinking water at a dose of 1.5 mg mL(-1) (200 mg kg(-1) bw). The NaNO3 -treated group showed a significant decrease in red blood cell count, hemoglobin and hematocrit and a significant increase in total white blood cell, in neutrophil and eosinophil counts. Platelet count, mean corpuscular volume, mean corpuscular hemoglobin, and mean corpuscular hemoglobin concentration remained unchanged in treated groups compared to those of controls. Meanwhile, the results showed a marked reduction in the antioxidant enzyme activities, such as superoxide dismutase, catalase, and glutathione peroxidase, along with an elevation in the level of lipid peroxidation and a reduction in the total glutathione content, indicating the induction of oxidative stress in the erythrocytes of NaNO3 -treated group. Interestingly, NaNO3 treatment showed a significant increase in the frequencies of total chromosomal aberrations, aberrant metaphases and micronucleus in bone-marrow cells. The oxidative stress induced by nitrate treatment might be the major cause for chromosomal rearrangements as free radicals leading to DNA damage. Hyparrhenia hirta methanolic extract appeared to be effective against hematotoxic and genotoxic changes induced by nitrate, as evidenced by the improvement of the markers cited above.
本研究旨在探讨水体硝酸盐污染对成年雄性大鼠的血液毒性和遗传毒性不良影响,以及使用希氏狼尾草甲醇提取物减轻这些影响。通过口服灌胃以400 mg kg⁻¹体重的剂量每日给成年大鼠施用硝酸钠(NaNO₃),持续50天,同时通过饮用水以1.5 mg mL⁻¹(200 mg kg⁻¹体重)的剂量给予希氏狼尾草甲醇提取物。NaNO₃处理组的红细胞计数、血红蛋白和血细胞比容显著降低,而总白细胞、中性粒细胞和嗜酸性粒细胞计数显著增加。与对照组相比,处理组的血小板计数、平均红细胞体积、平均红细胞血红蛋白和平均红细胞血红蛋白浓度保持不变。同时,结果显示抗氧化酶活性(如超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶)显著降低,同时脂质过氧化水平升高,总谷胱甘肽含量降低,表明NaNO₃处理组红细胞中诱导了氧化应激。有趣的是,NaNO₃处理显示骨髓细胞中总染色体畸变、异常中期和微核的频率显著增加。硝酸盐处理诱导的氧化应激可能是导致染色体重排的主要原因,因为自由基会导致DNA损伤。希氏狼尾草甲醇提取物似乎对硝酸盐诱导的血液毒性和遗传毒性变化有效,上述指标的改善证明了这一点。