首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Fluoride Affects Dopamine Metabolism and Causes Changes in the Expression of Dopamine Receptors (D1R and D2R) in Chosen Brain Structures of Morphine-Dependent Rats
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Fluoride Affects Dopamine Metabolism and Causes Changes in the Expression of Dopamine Receptors (D1R and D2R) in Chosen Brain Structures of Morphine-Dependent Rats

机译:氟化物影响吗啡依赖性大鼠所选脑结构中多巴胺代谢并导致多巴胺受体(D1R和D2R)表达的变化

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摘要

Disturbances caused by excess or shortages of certain elements can affect the cerebral reward system and may therefore modulate the processes associated with the development of dependence as was confirmed by behavioural studies on animals addicted to morphine. Earlier publications demonstrated and proved the neurodegenerative properties of both low and high doses of fluoride ions in animal experiments and in epidemiological and clinical studies. The aim of the experiments conducted in the course of the present study was to analyse the effect of pre- and postnatal exposure to 50 ppm F on the initiation/development of morphine dependence. For this purpose, the following were conducted: behavioural studies, the analysis of concentrations of dopamine and its metabolites, and the analyses of mRNA expression and dopamine receptor proteins D1 and D2 in the prefrontal cortex, striatum, hippocampus, and cerebellum of rats. In this study, it was observed for the first time that pre- and postnatal exposure to fluoride ions influenced the phenomenon of morphine dependence in a model expressing withdrawal symptoms. Behavioural, molecular, and neurochemical studies demonstrated that the degenerative changes caused by toxic activity of fluoride ions during the developmental period of the nervous system may impair the functioning of the dopaminergic pathway due to changes in dopamine concentration and in dopamine receptors. Moreover, the dopaminergic disturbances within the striatum and the cerebellum played a predominant role as both alterations of dopamine metabolism and profound alterations in striatal D1 and D2 receptors were discovered in these structures. The present study provides a new insight into a global problem showing direct associations between environmental factors and addictive disorders.
机译:由对吗啡上瘾的动物的行为研究证实,某些元素过多或不足引起的干扰会影响大脑的奖励系统,因此可能会调节与依赖性发展有关的过程。较早的出版物在动物实验以及流行病学和临床研究中证明并证明了低剂量和高剂量氟离子的神经退行性。在本研究过程中进行的实验的目的是分析出生前和出生后暴露于50 ppm F对吗啡依赖性起始/发展的影响。为此,进行了以下活动:行为研究,大鼠多巴胺及其代谢产物浓度的分析以及大鼠前额叶皮层,纹状体,海马和小脑中的mRNA表达和多巴胺受体蛋白D1和D2的分析。在这项研究中,首次观察到出生前和出生后暴露于氟离子会影响表达戒断症状的模型中吗啡依赖性现象。行为,分子和神经化学研究表明,在神经系统发育期间,由氟离子的有毒活性引起的变性变化可能会由于多巴胺浓度和多巴胺受体的变化而损害多巴胺能途径的功能。此外,纹状体和小脑内的多巴胺能紊乱起着主要作用,因为在这些结构中发现了多巴胺代谢的改变以及纹状体D1和D2受体的深刻改变。本研究为全球性问题提供了新的见解,该问题显示了环境因素与成瘾性疾病之间的直接关联。

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