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帕金森病和阿尔茨海默病中蓝斑核神经元丧失对中枢去甲肾上腺素能神经系统的不同反应。

Differential response of the central noradrenergic nervous system to the loss of locus coeruleus neurons in Parkinson's disease and Alzheimer's disease.

机构信息

Northwest Network for Mental Illness, Veterans Administration Puget Sound Health Care System, Seattle, Washington 98108, USA.

出版信息

Brain Res. 2011 Feb 10;1373:240-52. doi: 10.1016/j.brainres.2010.12.015. Epub 2010 Dec 11.

Abstract

In Parkinson's disease (PD), there is a significant loss of noradrenergic neurons in the locus coeruleus (LC) in addition to the loss of dopaminergic neurons in the substantia nigra (SN). The goal of this study was to determine if the surviving LC noradrenergic neurons in PD demonstrate compensatory changes in response to the neuronal loss, as observed in Alzheimer's disease (AD). Tyrosine hydroxylase (TH) and dopamine β-hydroxylase (DBH) mRNA expression in postmortem LC tissue of control and age-matched PD subjects demonstrated a significant reduction in the number of noradrenergic neurons in the LC of PD subjects. TH mRNA expression/neuron did not differ between control and PD subjects, but DBH mRNA expression/neuron was significantly elevated in PD subjects compared to control. This increase in DBH mRNA expression in PD subjects is not a response to neuronal loss because the amount of DBH mRNA expression/neuron in AD subjects was not significantly different from control. Norepinephrine transporter (NET) binding site concentration in the LC of PD subjects was significantly reduced over the cell body region as well as the peri-LC dendritic zone. In PD subjects, the loss of dendrites from surviving noradrenergic neurons was also apparent with TH-immunoreactivity (IR). This loss of LC dendritic innervation in PD subjects as measured by TH-IR was not due to LC neuronal loss because TH-IR in AD subjects was robust, despite a similar loss of LC neurons. These data suggest that there is a differential response of the noradrenergic nervous system in PD compared to AD in response to the loss of LC neurons.

摘要

在帕金森病(PD)中,除了黑质(SN)中的多巴胺能神经元丧失之外,蓝斑核(LC)中的去甲肾上腺素能神经元也有明显丧失。本研究的目的是确定 PD 中存活的 LC 去甲肾上腺素能神经元是否表现出与阿尔茨海默病(AD)中观察到的神经元丧失相适应的代偿性变化。在对照和年龄匹配的 PD 患者死后 LC 组织中,酪氨酸羟化酶(TH)和多巴胺-β-羟化酶(DBH)mRNA 表达显示,PD 患者 LC 中的去甲肾上腺素能神经元数量明显减少。TH mRNA 表达/神经元在对照和 PD 患者之间没有差异,但 PD 患者的 DBH mRNA 表达/神经元明显高于对照。PD 患者中 DBH mRNA 表达的增加不是神经元丧失的反应,因为 AD 患者的 DBH mRNA 表达/神经元数量与对照没有显著差异。PD 患者 LC 中的去甲肾上腺素转运体(NET)结合位点浓度在细胞体区域以及 LC 周围的树突区显著降低。在 PD 患者中,存活的去甲肾上腺素能神经元的树突丢失也与 TH-免疫反应性(IR)明显相关。PD 患者 LC 树突传入的这种丧失不是由于 LC 神经元丧失引起的,因为 AD 患者的 TH-IR 很强烈,尽管 LC 神经元也有类似的丧失。这些数据表明,与 AD 相比,PD 中 LC 神经元丧失时去甲肾上腺素能神经系统的反应存在差异。

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