铅引起大鼠大脑不同区域亚硝酸盐和硝酸盐水平的改变

S.M Chen, S Swilley, R Bell, S Rajanna, S.L.N Reddy , B Rajanna
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引用次数: 25

摘要

一氧化氮(NO)是一氧化氮合酶(NOS)在l-精氨酸转化为瓜氨酸过程中合成的一种自由基。铅(Pb)影响大鼠脑中的神经元功能。一氧化氮是一种神经信使,半衰期很短,会立即转化为亚硝酸盐和硝酸盐。本研究旨在通过测量大鼠脑小脑、海马、额叶皮层和脑干中亚硝酸盐和硝酸盐的含量来确定铅诱导一氧化氮生成的变化。雄性Sprague-Dawley大鼠腹腔注射醋酸铅(5和15 mg/kg体重量)。对照大鼠和实验大鼠分别于给药后7天和14天处死,分离不同脑区。采用noa280 (Sievers)化学发光法估算亚硝酸盐和硝酸盐(NOx)水平。数据表明,对铅的反应具有剂量依赖性和区域特异性。两种铅处理都降低了小脑和海马中的氮氧化物水平。然而,额叶皮质和脑干对铅暴露的反应不同。低剂量和高剂量Pb处理7天后,大鼠额叶皮层NOx水平显著升高,而14天后无显著升高,而脑干NOx水平呈剂量和时间依赖性升高。虽然,反应是时间依赖性的,但7天和14天治疗之间的差异并没有明确描述。这些结果提供了额外的证据,表明铅暴露会改变大鼠脑内no的产生,导致神经元功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lead induced alterations in nitrite and nitrate levels in different regions of the rat brain

Nitric oxide (NO) is a free radical synthesized by nitric oxide synthase (NOS) during the conversion of l-arginine to citrulline. Lead (Pb) affects neuronal functioning in the rat brain. Nitric oxide, a neuronal messenger has a short half life and converts immediately into nitrite and nitrate. The present study is designed to determine lead-induced alterations in NO production by measuring nitrite and nitrate in the cerebellum, the hippocampus, the frontal cortex and the brain stem of the rat brain. Male Sprague–Dawley rats were treated with lead acetate (5 and 15 mg/kg body wt.) by intraperitoneal injection. The control and experimental rats were sacrificed at the end of 7 and 14 days after treatment and different regions of the brain were isolated. Nitrite and nitrate (NOx) levels were estimated by the chemiluminescent method using the NOA 280 (Sievers). The data suggested dose-dependent and region-specific responses to lead. Both treatments of lead reduced NOx levels in the cerebellum and the hippocampus. However, the frontal cortex and the brain stem responded differently to Pb exposure. NOx levels in the frontal cortex were significantly increased in rats treated with low and high doses of Pb for 7 days but not in rats treated for 14 days, whereas in the brain stem, NOx levels were increased in a dose- and time-dependent manner. Although, the response was time-dependent, the variation between 7- and 14-day treatment was not clearly delineated. These results provide additional evidence that Pb exposure alters NO-production in rat brain leading to neuronal dysfunction.

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