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皮克病中的新皮质形态测量学与胆碱能神经化学

Neocortical morphometry and cholinergic neurochemistry in Pick's disease.

作者信息

Hansen L A, Deteresa R, Tobias H, Alford M, Terry R D

机构信息

Department of Neurosciences, University of California, San Diego, School of Medicine, La Jolla 92093.

出版信息

Am J Pathol. 1988 Jun;131(3):507-18.

PMID:3381880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1880699/
Abstract

With a computerized image-analysis apparatus for neocortical morphometry and chemical methods for evaluation of the cholinergic system, five brain specimens of Pick's disease (PD) were studied and the results compared to those from specimens of age-matched normal subjects and Alzheimer's disease (AD). The PD specimens showed major reductions in brain weight, frontal and temporal cortical thickness, and large neuron populations, compared with controls. Lesser reductions were seen in small neurons and thickness of the inferior parietal cortex. The authors found no relationship between age of onset or disease duration and either the degree of cortical thinning or neuron loss or the number of Pick bodies in the neocortex and hippocampus. PD specimens were more atrophic than AD brains, having lower brain weights and more fronto-temporal thinning. Large neurons were comparably reduced in the two conditions in the frontal and temporal lobes, but small neuron losses were greater in the PD midfrontal area. Only the AD cases showed loss of large neurons in the inferior parietal region. Levels of choline acetyltransferase were normal in PD and reduced in AD, whereas muscarinic receptor binding was decreased in both.

摘要

使用用于新皮质形态测量的计算机化图像分析设备以及评估胆碱能系统的化学方法,对五例匹克病(PD)脑标本进行了研究,并将结果与年龄匹配的正常受试者和阿尔茨海默病(AD)标本的结果进行了比较。与对照组相比,PD标本的脑重量、额叶和颞叶皮质厚度以及大神经元数量均有显著减少。顶下小叶皮质的小神经元和厚度减少程度较小。作者发现发病年龄或病程与皮质变薄程度、神经元丢失或新皮质和海马体中匹克小体的数量之间均无关联。PD标本比AD脑萎缩更严重,脑重量更低,额颞叶变薄更明显。额叶和颞叶的大神经元在两种情况下均有类似程度的减少,但PD额中部区域的小神经元丢失更严重。只有AD病例在顶下区域出现大神经元丢失。PD中胆碱乙酰转移酶水平正常,AD中则降低,而毒蕈碱受体结合在两者中均减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b932/1880699/c46545abb1ea/amjpathol00135-0143-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b932/1880699/6d3f972326e8/amjpathol00135-0142-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b932/1880699/c46545abb1ea/amjpathol00135-0143-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b932/1880699/6d3f972326e8/amjpathol00135-0142-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b932/1880699/c46545abb1ea/amjpathol00135-0143-a.jpg

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本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Neurochemical observations in a case of Pick's disease.一例匹克氏病的神经化学观察
J Neurol Sci. 1980 Nov;48(2):257-63. doi: 10.1016/0022-510x(80)90205-1.
3
Some morphometric aspects of the brain in senile dementia of the Alzheimer type.阿尔茨海默型老年痴呆症患者大脑的一些形态测量学特征。
J Neurochem. 2021 Sep;158(6):1394-1411. doi: 10.1111/jnc.15471. Epub 2021 Aug 6.
4
Appropriate use criteria for lumbar puncture and cerebrospinal fluid testing in the diagnosis of Alzheimer's disease.腰椎穿刺和脑脊液检测在阿尔茨海默病诊断中的合理应用标准。
Alzheimers Dement. 2018 Nov;14(11):1505-1521. doi: 10.1016/j.jalz.2018.07.220. Epub 2018 Oct 10.
5
The Past and the Future of Alzheimer's Disease Fluid Biomarkers.阿尔茨海默病液生物标志物的过去与未来。
J Alzheimers Dis. 2018;62(3):1125-1140. doi: 10.3233/JAD-170773.
6
Neurotransmitter deficits from frontotemporal lobar degeneration.来自额颞叶变性的神经递质缺失。
Brain. 2018 May 1;141(5):1263-1285. doi: 10.1093/brain/awx327.
7
Diagnosis and management of behavioral variant frontotemporal dementia.行为变异型额颞叶痴呆的诊断与管理
Biol Psychiatry. 2014 Apr 1;75(7):574-81. doi: 10.1016/j.biopsych.2013.11.006. Epub 2013 Nov 13.
8
Management of frontotemporal dementia: targeting symptom management in such a heterogeneous disease requires a wide range of therapeutic options.额颞叶痴呆的管理:在这种异质性疾病中针对症状管理需要广泛的治疗选择。
Neurodegener Dis Manag. 2011 Apr;1(2):141-156. doi: 10.2217/nmt.11.9.
9
Abhorring the vacuum: use of Alzheimer’s disease medications in frontotemporal dementia.厌恶空洞:阿尔茨海默病药物在前额颞叶痴呆中的应用。
Expert Rev Neurother. 2011 May;11(5):709-17. doi: 10.1586/ern.11.6.
10
Medical management of frontotemporal dementias: the importance of the caregiver in symptom assessment and guidance of treatment strategies.额颞叶痴呆的医学管理:照顾者在症状评估和治疗策略指导中的重要性。
J Mol Neurosci. 2011 Nov;45(3):713-23. doi: 10.1007/s12031-011-9558-7. Epub 2011 Jun 7.
Ann Neurol. 1981 Aug;10(2):184-92. doi: 10.1002/ana.410100209.
4
Choline acetyltransferase activity and histopathology of frontal neocortex from biopsies of demented patients.痴呆患者活检额叶新皮质的胆碱乙酰转移酶活性与组织病理学
J Neurol Sci. 1982 Dec;57(2-3):191-202. doi: 10.1016/0022-510x(82)90026-0.
5
A search for discrete cholinergic nuclei in the human ventral forebrain.对人类腹侧前脑离散胆碱能核的研究。
J Neurochem. 1982 Dec;39(6):1743-7. doi: 10.1111/j.1471-4159.1982.tb08013.x.
6
Alzheimer's disease and senile dementia: loss of neurons in the basal forebrain.阿尔茨海默病和老年痴呆症:基底前脑神经元的丧失。
Science. 1982 Mar 5;215(4537):1237-9. doi: 10.1126/science.7058341.
7
Fibrous Astrocytes in senile dementia of the Alzheimer type.阿尔茨海默型老年痴呆症中的纤维性星形胶质细胞。
J Neuropathol Exp Neurol. 1981 Mar;40(2):95-101. doi: 10.1097/00005072-198103000-00002.
8
Cortical neuronal counts in normal elderly controls and demented patients.正常老年对照组和痴呆患者的皮质神经元计数。
Neurobiol Aging. 1983 Spring;4(1):1-11. doi: 10.1016/0197-4580(83)90048-9.
9
A comparison of changes in the nucleus basalis and locus caeruleus in Alzheimer's disease.阿尔茨海默病中基底核与蓝斑核变化的比较。
J Neurol Neurosurg Psychiatry. 1984 Feb;47(2):201-3. doi: 10.1136/jnnp.47.2.201.
10
Pick's disease (lobar sclerosis): depletion of neurons in the nucleus basalis of Meynert.皮克病(叶性硬化症):迈内特基底核神经元缺失。
Neurology. 1983 Nov;33(11):1470-3. doi: 10.1212/wnl.33.11.1470.