Laboratorio de Biología Celular y Molecular, Facultad de Ciencias Químicas, Universidad Juárez del Estado de Durango, Av. Artículo 123 s/n Fracc. Filadelfia, C.P. 35010 Gómez Palacio, Durango, Mexico.
Laboratorio de Biología Evolutiva, Facultad de Ciencias Biológicas, Universidad Juárez del Estado de Durango, Av. Universidad s/n., Gómez Palacio, Durango, Mexico.
Ecotoxicol Environ Saf. 2018 Dec 30;166:48-55. doi: 10.1016/j.ecoenv.2018.09.060. Epub 2018 Sep 20.
Nitrate pollution has emerged as a problem of great importance because in recent years, the levels of nitrate in soil and groundwater have increased, mainly through anthropogenic activities, such as the use of fertilizers in agriculture, domestic wastewater and septic tanks, industrial waste and deforestation. In animals, nitrate reduction to nitrite (NO) and nitric oxide (NO) promote the formation of methemoglobin in the blood and the generation of highly reactive intermediates that induce oxidative stress in target organs. Exposition to nitrates has been associated with methemoglobinemia, reproductive toxicity, metabolic and endocrine alterations and cancer. This study analyzed acute intoxication with sodium nitrate (NaNO) in male Wistar rats, aged 12-16 weeks. Four groups with n = 10 rats each were formed: group 1 was the control, and group 2, group 3 and group 4 were treated for 10 days with intragastric doses of 19, 66 and 150 mg/kg/d NaNO, respectively. Hematological, metabolic and histological biomarkers in the liver were analyzed. The results showed high percentages of methemoglobin, an increase in NO in the plasma and an accumulation in the liver. Moreover, there were high counts of white blood cells and platelets in all treated groups. Additionally, there was an increase in the spleen weight in group 4. High levels of glucose, triglycerides, lactate dehydrogenase (LDH), alanine aminotransferase (ALT), and aspartate aminotransferase (AST) were observed and were significantly increased in groups 3 and 4. For oxidative stress biomarkers, there were increases in Thiobarbituric Acid Reactive Substances (TBARS), total GSH and SOD activity, mainly in group 4. Changes in mitochondrial activity were not significant. Histopathological analyses of the liver showed inflammation, infiltration of mononuclear cells, steatosis, ischemia and necrosis, and these findings were more evident at high doses of NaNO in which high of S-nitrosylation were found. In conclusion, NaNO was reduced to NO, thereby inducing methemoglobinemia, whereas other reactive species generated oxidative stress, causing hematological and metabolic alterations and injury to the liver.
硝酸盐污染已成为一个非常重要的问题,因为近年来,土壤和地下水中的硝酸盐含量增加,主要是由于人为活动,如农业中使用化肥、生活污水和化粪池、工业废物和森林砍伐。在动物中,硝酸盐还原为亚硝酸盐(NO)和一氧化氮(NO)会促进血液中高铁血红蛋白的形成,并生成诱导靶器官氧化应激的高反应性中间产物。暴露于硝酸盐与高铁血红蛋白血症、生殖毒性、代谢和内分泌改变以及癌症有关。本研究分析了雄性 Wistar 大鼠急性摄入硝酸钠(NaNO)的情况,大鼠年龄为 12-16 周。形成了 4 组,每组 10 只大鼠:第 1 组为对照组,第 2、3 和 4 组分别经口给予 19、66 和 150mg/kg/d NaNO 治疗 10 天。分析了肝脏的血液学、代谢和组织学生物标志物。结果显示高铁血红蛋白百分比高、血浆中 NO 增加且在肝脏中蓄积。此外,所有治疗组的白细胞和血小板计数均升高。此外,第 4 组的脾脏重量增加。观察到葡萄糖、甘油三酯、乳酸脱氢酶(LDH)、丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)水平升高,第 3 和第 4 组的水平显著升高。对于氧化应激生物标志物,硫代巴比妥酸反应物质(TBARS)、总 GSH 和 SOD 活性增加,主要在第 4 组中增加。线粒体活性的变化不明显。肝脏组织病理学分析显示炎症、单核细胞浸润、脂肪变性、缺血和坏死,这些发现在 NaNO 高剂量下更为明显,其中发现了大量的 S-亚硝基化。总之,NaNO 被还原为 NO,从而诱导高铁血红蛋白血症,而其他活性物质则产生氧化应激,导致血液学和代谢改变以及肝脏损伤。