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首页> 外文期刊>Neurotoxicology >Duration of airborne-manganese exposure in rhesus monkeys is associated with brain regional changes in biomarkers of neurotoxicity.
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Duration of airborne-manganese exposure in rhesus monkeys is associated with brain regional changes in biomarkers of neurotoxicity.

机译:恒河猴中空气中锰暴露的持续时间与神经毒性生物标志物的脑区域变化有关。

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Juvenile (20-24-month-old) rhesus monkeys were exposed to airborne-manganese sulfate (MnSO(4)) 1.5 mg Mn/m(3) (6h/day, 5 days/week) for 15 or 33 days, or for 65 days followed by a 45 or 90 days post-exposure recovery period, or air. We assessed biochemical endpoints indicative of oxidative stress and excitotoxicity in the cerebellum, frontal cortex, caudate, globus pallidus, olfactory cortex, and putamen. Glutamine synthetase (GS), glutamate transporters (GLT-1 and GLAST) and tyrosine hydroxylase (TH) protein levels, metallothionein (MT), GLT-1, GLAST, TH and GS mRNA levels, and total glutathione (GSH) levels were determined for all brain regions. Exposure to Mn significantly decreased MT mRNA in the caudate (vs. air-exposed controls). This depression persisted at least 90 days post-exposure. In contrast, putamen MT mRNA levels were unaffected by Mn exposure. GLT-1 and GLAST were relatively unaffected by short term Mn exposure, except in the globus pallidus where exposure for 33 days led to decreased protein levels, which persisted after 45 days of recovery for both proteins and 90 days of recovery in the case of GLAST. Exposure to 1.5 mg Mn/m(3) caused a significant decrease in GSH levels in the caudate and increased GSH levels in the putamen of monkey exposed for 15 and 33 days with both effects persisting at least 90 days post-exposure. Finally, TH protein levels were significantly lowered in the globus pallidus of the monkeys exposed for 33 days but mRNA levels were significantly increased in this same region. Overall, the nonhuman primate brain responds to airborne Mn in a heterogeneous manner and most alterations in these biomarkers of neurotoxicity are reversible upon cessation of Mn exposure.
机译:将幼年(20-24个月大)的恒河猴暴露于空气中的硫酸锰(MnSO(4))1.5 mg Mn / m(3)(6h / day,5 days / week),持续15或33天,或持续65天,然后在暴露后恢复期45或90天或空气中。我们评估了指示小脑,额叶皮层,尾状,苍白球,嗅皮层和壳状核中的氧化应激和兴奋性毒性的生化终点。确定了谷氨酰胺合成酶(GS),谷氨酸转运蛋白(GLT-1和GLAST)和酪氨酸羟化酶(TH)的蛋白质水平,金属硫蛋白(MT),GLT-1,GLAST,TH和GS mRNA的水平以及总谷胱甘肽(GSH)的水平适用于所有大脑区域。暴露于锰会显着降低尾状体中的MT mRNA(相对于空气暴露的对照)。暴露后这种抑郁症至少持续90天。相比之下,壳聚糖MT mRNA水平不受锰暴露的影响。 GLT-1和GLAST相对不受短期Mn暴露的影响,但在苍白球中暴露33天会导致蛋白质水平降低,这两种蛋白质在恢复45天后均持续存在,而在GLAST情况下恢复90天后持续存在。暴露于1.5 mg Mn / m(3)会导致尾状骨中的GSH含量显着降低,而暴露于猴子15和33天的壳状果壳中的GSH含量则显着增加,并且两种作用在暴露后至少持续90天。最后,暴露33天的猴的苍白球中TH蛋白水平显着降低,但是在该相同区域中,mRNA水平显着升高。总体而言,非人类的灵长类动物大脑以不同的方式对空气中的Mn做出反应,这些神经毒性生物标志物中的大多数改变在Mn暴露停止后是可逆的。

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