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1
Neuronal hypertrophy in asymptomatic Alzheimer disease.无症状阿尔茨海默病中的神经元肥大
J Neuropathol Exp Neurol. 2008 Jun;67(6):578-89. doi: 10.1097/NEN.0b013e3181772794.
2
Synaptic contact number and size in stratum radiatum CA1 of APP/PS1DeltaE9 transgenic mice.APP/PS1DeltaE9转基因小鼠海马CA1区辐射层的突触接触数量和大小
Neurobiol Aging. 2009 Nov;30(11):1756-76. doi: 10.1016/j.neurobiolaging.2008.01.009. Epub 2008 Mar 11.
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Amyloid precursor protein increases cortical neuron size in transgenic mice.淀粉样前体蛋白可增加转基因小鼠的皮质神经元大小。
Neurobiol Aging. 2009 Aug;30(8):1238-44. doi: 10.1016/j.neurobiolaging.2007.12.024. Epub 2008 Mar 4.
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Roles of autophagy and mTOR signaling in neuronal differentiation of mouse neuroblastoma cells.自噬和mTOR信号通路在小鼠神经母细胞瘤细胞神经元分化中的作用
Cell Signal. 2008 Apr;20(4):659-65. doi: 10.1016/j.cellsig.2007.11.015. Epub 2008 Jan 22.
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Neurotrophic factors in Alzheimer's disease: role of axonal transport.阿尔茨海默病中的神经营养因子:轴突运输的作用
Genes Brain Behav. 2008 Feb;7 Suppl 1(1):43-56. doi: 10.1111/j.1601-183X.2007.00378.x.
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Synaptic proteins, neuropathology and cognitive status in the oldest-old.高龄老人的突触蛋白、神经病理学与认知状态
Neurobiol Aging. 2009 Jul;30(7):1125-34. doi: 10.1016/j.neurobiolaging.2007.10.001. Epub 2007 Nov 14.
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Paradoxical upregulation of glutamatergic presynaptic boutons during mild cognitive impairment.轻度认知障碍期间谷氨酸能突触前终扣的反常上调
J Neurosci. 2007 Oct 3;27(40):10810-7. doi: 10.1523/JNEUROSCI.3269-07.2007.
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Cellular and subcellular change evoked by diffuse traumatic brain injury: a complex web of change extending far beyond focal damage.弥漫性创伤性脑损伤引起的细胞和亚细胞变化:一个远远超出局灶性损伤的复杂变化网络。
Prog Brain Res. 2007;161:43-59. doi: 10.1016/S0079-6123(06)61004-2.
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Resistance to Alzheimer's pathology is associated with nuclear hypertrophy in neurons.对阿尔茨海默病病理的抵抗与神经元中的核肥大有关。
Neurobiol Aging. 2007 Oct;28(10):1484-92. doi: 10.1016/j.neurobiolaging.2007.05.005. Epub 2007 Jun 28.
10
Synaptic alterations in CA1 in mild Alzheimer disease and mild cognitive impairment.轻度阿尔茨海默病和轻度认知障碍中CA1区的突触改变。
Neurology. 2007 May 1;68(18):1501-8. doi: 10.1212/01.wnl.0000260698.46517.8f.

修女研究:临床无症状性阿尔茨海默病、神经元肥大与早年语言技能

The Nun study: clinically silent AD, neuronal hypertrophy, and linguistic skills in early life.

作者信息

Iacono D, Markesbery W R, Gross M, Pletnikova O, Rudow G, Zandi P, Troncoso J C

机构信息

Division of Neuropathology, Department of Pathology, Johns Hopkins University, School of Medicine, Ross Building 558, 720 Rutland Avenue, Baltimore, MD 21205, USA.

出版信息

Neurology. 2009 Sep 1;73(9):665-73. doi: 10.1212/WNL.0b013e3181b01077. Epub 2009 Jul 8.

DOI:10.1212/WNL.0b013e3181b01077
PMID:19587326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2734290/
Abstract

BACKGROUND

It is common to find substantial Alzheimer disease (AD) lesions, i.e., neuritic beta-amyloid plaques and neurofibrillary tangles, in the autopsied brains of elderly subjects with normal cognition assessed shortly before death. We have termed this status asymptomatic AD (ASYMAD). We assessed the morphologic substrate of ASYMAD compared to mild cognitive impairment (MCI) in subjects from the Nun Study. In addition, possible correlations between linguistic abilities in early life and the presence of AD pathology with and without clinical manifestations in late life were considered.

METHODS

Design-based stereology was used to measure the volumes of neuronal cell bodies, nuclei, and nucleoli in the CA1 region of hippocampus (CA1). Four groups of subjects were compared: ASYMAD (n = 10), MCI (n = 5), AD (n = 10), and age-matched controls (n = 13). Linguistic ability assessed in early life was compared among all groups.

RESULTS

A significant hypertrophy of the cell bodies (+44.9%), nuclei (+59.7%), and nucleoli (+80.2%) in the CA1 neurons was found in ASYMAD compared with MCI. Similar differences were observed with controls. Furthermore, significant higher idea density scores in early life were observed in controls and ASYMAD group compared to MCI and AD groups.

CONCLUSIONS

  1. Neuronal hypertrophy may constitute an early cellular response to Alzheimer disease (AD) pathology or reflect compensatory mechanisms that prevent cognitive impairment despite substantial AD lesions; 2) higher idea density scores in early life are associated with intact cognition in late life despite the presence of AD lesions.
摘要

背景

在死亡前不久认知功能正常的老年受试者尸检大脑中,常常发现大量阿尔茨海默病(AD)病变,即神经炎性β-淀粉样斑块和神经原纤维缠结。我们将这种状态称为无症状AD(ASYMAD)。我们在修女研究的受试者中,评估了ASYMAD与轻度认知障碍(MCI)相比的形态学基础。此外,还考虑了早年语言能力与晚年有无临床表现的AD病理学之间的可能相关性。

方法

采用基于设计的体视学方法测量海马CA1区神经元细胞体、细胞核和核仁的体积。比较了四组受试者:ASYMAD(n = 10)、MCI(n = 5)、AD(n = 10)和年龄匹配的对照组(n = 13)。比较了所有组早年评估的语言能力。

结果

与MCI相比,ASYMAD中CA1神经元的细胞体(+44.9%)、细胞核(+59.7%)和核仁(+80.2%)显著肥大。与对照组也观察到类似差异。此外,与MCI组和AD组相比,对照组和ASYMAD组早年的观念密度得分显著更高。

结论

1)神经元肥大可能是对阿尔茨海默病(AD)病理学的早期细胞反应,或反映了尽管存在大量AD病变但仍能防止认知障碍的代偿机制;2)尽管存在AD病变,但早年较高的观念密度得分与晚年认知功能完整有关。