Ríos R, Zarazúa S, Santoyo M E, Sepúlveda-Saavedra J, Romero-Díaz V, Jiménez V, Pérez-Severiano F, Vidal-Cantú G, Delgado J M, Jiménez-Capdeville M E
Departamento de Bioquímica, Facultad de Medicina, Universidad Autónoma de San Luis Potosí, Av. V. Carranza 2405, Col. Los Filtros, 78210 San Luis Potosí, S.L.P., Mexico.
Toxicology. 2009 Jun 30;261(1-2):68-75. doi: 10.1016/j.tox.2009.04.055. Epub 2009 May 3.
Epidemiological studies demonstrate an association between chronic consumption of arsenic contaminated water and cognitive deficits, especially when the exposure takes place during childhood. This study documents structural changes and nitrergic deficits in the striatum of adult female Wistar rats exposed to arsenic in drinking water (3 ppm, approximately 0.4 mg/kg per day) from gestation, throughout lactation and development until the age of 4 months. Kainic acid injected animals (10mg/kg, i.p.) were also analyzed as positive controls of neural cell damage. Morphological characteristics of cells, fiber tracts and axons were analyzed by means of light microscopy as well as immunoreactivity to neuronal nitric oxide synthase (nNOS). As nitrergic markers, nitrite/nitrate concentrations, nNOS levels and expression of nNOS-mRNA were quantified in striatal tissue. Reactive oxygen species (ROS) and lipid peroxidation (LPx) were determined as oxidative stress markers. Arsenic exposure resulted in moderate to severe alterations of thickness, organization, surrounding space and shape of fiber tracts and axons, while cell bodies remained healthy. These anomalies were not accompanied by ROS and/or LPx increases. By contrast, except the expression of nNOS-mRNA, all nitrergic markers including striatal nNOS immunoreactivity presented a significant decrease. These results indicate that arsenic targets the central nitrergic system and disturbs brain structural organization at low exposure levels.
流行病学研究表明,长期饮用受砷污染的水与认知缺陷之间存在关联,尤其是在儿童期接触砷时。本研究记录了成年雌性Wistar大鼠从妊娠期开始,在整个哺乳期和发育过程中直至4个月龄,饮用含砷(3 ppm,约0.4 mg/kg/天)的水后纹状体的结构变化和一氧化氮能缺陷。注射 kainic 酸的动物(10mg/kg,腹腔注射)也作为神经细胞损伤的阳性对照进行了分析。通过光学显微镜以及对神经元型一氧化氮合酶(nNOS)的免疫反应性分析细胞、纤维束和轴突的形态特征。作为一氧化氮能标记物,对纹状体组织中的亚硝酸盐/硝酸盐浓度、nNOS水平和nNOS-mRNA表达进行了定量。测定了活性氧(ROS)和脂质过氧化(LPx)作为氧化应激标记物。砷暴露导致纤维束和轴突的厚度、组织结构、周围空间和形状出现中度至重度改变,而细胞体保持健康。这些异常并未伴随着ROS和/或LPx的增加。相比之下,除了nNOS-mRNA的表达外,所有一氧化氮能标记物,包括纹状体nNOS免疫反应性均显著降低。这些结果表明,砷在低暴露水平下靶向中枢一氧化氮能系统并扰乱脑结构组织。