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阿尔茨海默病中的神经受体变化

Neuroreceptor changes in Alzheimer disease.

作者信息

Nordberg A

机构信息

Department of Pharmacology, Uppsala University, Sweden.

出版信息

Cerebrovasc Brain Metab Rev. 1992 Winter;4(4):303-28.

PMID:1486017
Abstract

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.

摘要

阿尔茨海默病存在多种神经受体变化。这些观察结果基于对尸检脑组织的分析,较少基于神经外科活检。尸检材料信息的缺点在于,受体变化代表了痴呆症的终末期。因此,基于这些发现制定治疗策略可能会有一定误导性。有望如正电子发射断层扫描(PET)和单光子发射断层扫描(SPECT)等新的成像技术能从疾病早期进程提供有价值的新的体内数据。在阿尔茨海默病中发生变化的递质系统中,胆碱能系统显示出最一致的缺陷。胆碱能毒蕈碱受体在阿尔茨海默病大脑中似乎得以保留,而烟碱受体则有损失。血清素(5-HT1和5-HT2)和谷氨酸受体的数量也减少。有趣的是,在皮质阿尔茨海默病组织中,海人藻酸受体数量增加而NMDA受体减少。阿尔茨海默病中所有受体变化的共同之处在于,结合位点数量发生变化,而亲和常数保持不变。α和β受体以及多巴胺受体在阿尔茨海默病大脑中相对得以保留。在神经肽中,已报道生长抑素和神经肽Y(NPY)的受体位点有损失。有趣的是,在阿尔茨海默病大脑的皮质区域,促肾上腺皮质激素释放因子(CRF)受体数量增加。因此,毒蕈碱(M1)、海人藻酸和CRF受体可能由于阿尔茨海默病中的退行性反应而显示出受体代偿反应。很少有人尝试在阿尔茨海默病患者体内可视化神经受体。然而,该领域正在动态发展。通过PET和[11C] - 尼古丁已在阿尔茨海默病患者大脑中可视化烟碱受体数量减少,并证实了早期在死后脑组织中的观察结果。轻度痴呆患者中,与(S)( - )[11C]尼古丁相比,(R)( + )[11C]尼古丁摄取较低可能是一种可能的诊断标志物。SPECT研究表明阿尔茨海默病大脑中毒蕈碱受体得以保留。对周围非神经组织中神经受体变化的分析表明,从阿尔茨海默病患者获得的外周淋巴细胞中烟碱和毒蕈碱受体减少。

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