阿尔茨海默病的神经受体变化。

A Nordberg
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引用次数: 0

摘要

阿尔茨海默病中存在多种神经受体改变。这些观察结果是基于尸检脑组织的分析,或者更少来自神经外科活检。从尸检材料中获得的信息的缺点是,受体的变化代表了痴呆症的最后阶段。因此,根据这些发现制定治疗策略可能有些误导。希望新的成像技术,如正电子发射断层扫描(PET)和单光子发射断层扫描(SPECT)将提供有价值的新的体内数据,从疾病的早期过程。在阿尔茨海默病改变的递质系统中,胆碱能系统显示出最一致的缺陷。胆碱能毒蕈碱受体似乎在阿尔茨海默氏症大脑中保留了下来,而尼古丁受体则丢失了。血清素(5-HT1和5-HT2)和谷氨酸受体的数量也减少。有趣的是,海碱盐受体数量增加,而NMDA受体在阿尔茨海默病皮层组织中减少。阿尔茨海默病中所有受体变化的共同点是,结合位点的数量发生变化,而亲和力常数保持不变。-受体和-受体以及多巴胺受体在阿尔茨海默症患者的大脑中相对保存了下来。在神经肽中,生长抑素和神经肽Y (NPY)的受体位点缺失已被报道。有趣的是,在阿尔茨海默症患者的大脑皮层区域,CRF受体的数量有所增加。因此,毒蕈碱(M1)、海碱盐和CRF受体可能由于阿尔茨海默病的退行性反应而表现出受体代偿反应。很少有人尝试可视化阿尔茨海默病患者体内的神经受体。然而,这一领域正处于动态发展之中。通过PET和[11C]-尼古丁,在阿尔茨海默病患者的大脑中发现了尼古丁受体数量的减少,并证实了早期在死后脑组织中的观察结果。轻度痴呆患者对(R)(+)[11C]尼古丁的摄取低于(S)(-)[11C]尼古丁,这可能是一种可能的诊断标志。SPECT研究表明阿尔茨海默病大脑中保留了毒蕈碱受体。外周非神经组织的神经受体变化分析显示,从阿尔茨海默病患者获得的外周淋巴细胞中尼古丁和毒蕈碱受体减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroreceptor changes in Alzheimer disease.

Multiple neuroreceptor changes are present in Alzheimer disease. These observations are based upon analysis from autopsy brain tissue or more seldom from neurosurgical biopsies. The drawback of information from autopsy material is that the receptor changes represent the final stage of the dementia disorder. It might therefore be somewhat misleading to base therapeutic strategies on these findings. Hopefully, new imaging techniques such as positron emission tomography (PET) and single photon emission tomography (SPECT) will provide valuable new in vivo data from the earlier course of the disease. Among the transmitter systems changed in Alzheimer disease, the cholinergic system shows the most consistent deficits. Cholinergic muscarinic receptors seem to be preserved in Alzheimer brains while nicotinic receptors show losses. The number of serotonin (both 5-HT1 and 5-HT2) and glutamate receptors are also reduced. Interestingly, kainate receptors increase in number while NMDA receptors are reduced in cortical Alzheimer tissue. Common for all receptor changes in Alzheimer disease is that the changes in number of binding sites are seen while the affinity constant remains unchanged. alpha- and beta-receptors and dopamine receptors are relatively preserved in Alzheimer brains. Among the neuropeptides, losses in receptor sites have been reported for somatostatin and neuropeptide Y (NPY). Interestingly, the number of CRF receptors are increased in cortical areas of Alzheimer brains. Thus, the muscarinic (M1), kainate, and CRF receptors show receptor compensatory reactions probably due to degenerative reactions in Alzheimer disease. Few attempts have been made to visualize neuroreceptors in vivo in Alzheimer patients. The field, however, is in dynamic progress. Reduced numbers of nicotinic receptors have been visualized in the brain of Alzheimer patients by PET and [11C]-nicotine and confirm earlier observations in post-mortem brain tissues. A lower uptake of (R)(+)[11C]nicotine compared to (S)(-)[11C]nicotine in patients with a mild form of dementia might be a possible diagnostic marker. SPECT studies indicate preserved muscarinic receptors in Alzheimer brains. Analysis of neuroreceptor changes in peripheral nonneural tissues have shown a reduction in nicotinic and muscarinic receptors in peripheral lymphocytes obtained from Alzheimer patients.

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