首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Dysregulation of Dopaminergic Regulatory Factors TH Nurr1 and Pitx3 in the Ventral Tegmental Area Associated with Neuronal Injury Induced by Chronic Morphine Dependence
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Dysregulation of Dopaminergic Regulatory Factors TH Nurr1 and Pitx3 in the Ventral Tegmental Area Associated with Neuronal Injury Induced by Chronic Morphine Dependence

机译:多巴胺能调节因子THNurr1和Pitx3在慢性被吗啡依赖引起的神经元损伤相关的腹侧被盖区的失调。

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摘要

The ventral tegmental area (VTA), a critical portion of the mesencephalic dopamine system, is thought to be involved in the development and maintenance of addiction. It has been proposed that the dopaminergic regulatory factors TH, Nurr1, and Pitx3 are crucial for determining the survival and maintenance of dopaminergic neurons. Thus, the present study investigated whether abnormalities in these dopaminergic regulatory factors in the VTA were associated with neuronal injury induced by chronic morphine dependence. Rat models with different durations of morphine dependence were established. Thionine staining was used to observe morphological changes in the VTA neurons. Immunohistochemistry and western blot were used to observe changes in the expression of the dopaminergic regulatory proteins TH, Nurr1, and Pitx3. Thionine staining revealed that prolonged morphine dependence resulted in dopaminergic neurons with edema, a lack of Nissl bodies, and pyknosis. Immunohistochemistry showed that the number of TH+, Nurr1+, and Pitx3+ cells, and the number of TH+ cells expressing Nurr1 or Pitx3, significantly decreased in the VTA after a long period of morphine dependence. Western blot results were consistent with the immunohistochemistry findings. Chronic morphine exposure resulted in abnormalities in dopaminergic regulatory factors and pathological changes in dopaminergic neurons in the VTA. These results suggest that dysregulation of dopaminergic regulatory factors in the VTA are associated with neuronal injury induced by chronic morphine dependence.
机译:腹侧被盖区(VTA)是中脑多巴胺系统的关键部分,被认为与成瘾的发展和维持有关。已经提出,多巴胺能调节因子TH,Nurr1和Pitx3对于确定多巴胺能神经元的存活和维持至关重要。因此,本研究调查了VTA中这些多巴胺能调节因子的异常是否与慢性吗啡依赖引起的神经元损伤有关。建立了具有不同吗啡依赖持续时间的大鼠模型。硫氨酸染色用于观察VTA神经元的形态变化。免疫组化和免疫印迹用于观察多巴胺能调节蛋白TH,Nurr1和Pitx3表达的变化。蛋氨酸染色表明,吗啡依赖时间延长会导致多巴胺能神经元出现水肿,尼氏体缺乏和萎缩。免疫组化显示TH + ,Nurr1 + 和Pitx3 + 细胞的数量以及TH + 的数量在长时间的吗啡依赖后,表达Nurr1或Pitx3的细胞在VTA中显着减少。蛋白质印迹结果与免疫组织化学结果一致。慢性吗啡暴露会导致VTA中多巴胺能调节因子异常和多巴胺能神经元的病理变化。这些结果表明,VTA中多巴胺能调节因子的失调与慢性吗啡依赖引起的神经元损伤有关。

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