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首页> 外文期刊>Neuropsychopharmacology >Loss of Dopamine D2 Receptors in Alzheimer's Disease with Parkinsonism But Not Parkinson's or Alzheimer's Disease
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Loss of Dopamine D2 Receptors in Alzheimer's Disease with Parkinsonism But Not Parkinson's or Alzheimer's Disease

机译:多巴胺D2受体在帕金森氏症但不是帕金森氏症或阿尔茨海默氏病中的丢失

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A significant proportion of patients with Alzheimer's disease (AD) exhibit extrapyramidal features that are referred to as parkinsonism (AD/Park) to distinguish the clinical and pathological features that differ from Parkinson's disease (PD). Previous results from this laboratory have shown that, although the presynaptic components of the dopamine (DA) system are markedly affected in AD/Park, the pathology is not similar to PD (Murray et al. 1995; Joyce et al. 1997). In the present study, we determined whether the parkinsonian symptoms in AD/Park might also reflect changes in numbers of postsynaptic DA receptors. We analyzed the binding of [125I]epidepride biding to DA D2/D3 receptors and [3H]SCH 23390 to D1 receptors by autoradiography in the striatum of six patients with PD, nine patients with AD, seven patients with AD/Park, and 14 neurologically intact control subjects. D2 receptors were reduced in the caudate and putamen of the AD/Park group (by 42 and 27% of controls, respectively) but not reduced in AD or PD. D1 receptors were elevated by 36% in the putamen of the PD group. Dopamine receptor changes are, therefore, not similar in PD, AD, and AD/Park. The elevation in D1 receptors in PD may contribute to the unwanted side effects of L-dopa treatment. The loss of D2 receptors in AD/Park, not observed in AD lacking overt parkinsonian symptomatology, may contribute to the presence of parkinsonian features and lack of responsiveness to L-dopa.
机译:很大一部分阿尔茨海默氏病(AD)患者表现出锥体外系特征,被称为帕金森综合症(AD / Park),以区别于帕金森氏病(PD)的临床和病理特征。该实验室的先前结果表明,尽管多巴胺(DA)系统的突触前成分在AD / Park中受到显着影响,但其病理学与PD并不相似(Murray等,1995; Joyce等,1997)。在本研究中,我们确定AD / Park中的帕金森氏症是否也可能反映突触后DA受体数量的变化。我们通过放射自显影分析了6例PD患者,9例AD患者,7例AD / Park患者和14例患者纹状体中[125I]表肽与DA D2 / D3受体和[3H] SCH 23390与D1受体的结合。神经学上完整的对照对象。在AD / Park组的尾状和壳状核中,D2受体降低(分别为对照组的42%和27%),但在AD或PD中则没有降​​低。 PD组的壳核中D1受体升高了36%。因此,在PD,AD和AD / Park中,多巴胺受体的变化并不相似。 PD中D1受体的升高可能导致左旋多巴治疗的不良副作用。在缺乏明显帕金森病症状的AD中未观察到AD / Park中D2受体的丢失,可能导致帕金森病特征的存在和对L-多巴缺乏反应性。

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