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本文引用的文献

1
Locus ceruleus degeneration promotes Alzheimer pathogenesis in amyloid precursor protein 23 transgenic mice.蓝斑核变性促进淀粉样前体蛋白23转基因小鼠的阿尔茨海默病发病机制。
J Neurosci. 2006 Feb 1;26(5):1343-54. doi: 10.1523/JNEUROSCI.4236-05.2006.
2
The PDAPP mouse model of Alzheimer's disease: locus coeruleus neuronal shrinkage.阿尔茨海默病的PDAPP小鼠模型:蓝斑神经元萎缩。
J Comp Neurol. 2005 Nov 28;492(4):469-76. doi: 10.1002/cne.20744.
3
Stereological analysis of microvascular parameters in a double transgenic model of Alzheimer's disease.阿尔茨海默病双转基因模型中微血管参数的体视学分析
Brain Res Bull. 2005 Apr 30;65(4):317-22. doi: 10.1016/j.brainresbull.2004.11.024.
4
Mouse models of Alzheimer's disease: insight into treatment.阿尔茨海默病的小鼠模型:对治疗的洞察
Rev Neurosci. 2004;15(5):353-69. doi: 10.1515/revneuro.2004.15.5.353.
5
Massive CA1/2 neuronal loss with intraneuronal and N-terminal truncated Abeta42 accumulation in a novel Alzheimer transgenic model.在一种新型阿尔茨海默病转基因模型中,CA1/2区出现大量神经元丢失,伴有神经元内和N端截短的β淀粉样蛋白4 (Abeta42) 积聚。
Am J Pathol. 2004 Oct;165(4):1289-300. doi: 10.1016/s0002-9440(10)63388-3.
6
Hippocampal neuron loss exceeds amyloid plaque load in a transgenic mouse model of Alzheimer's disease.在阿尔茨海默病转基因小鼠模型中,海马体神经元损失超过淀粉样斑块负荷。
Am J Pathol. 2004 Apr;164(4):1495-502. doi: 10.1016/S0002-9440(10)63235-X.
7
Building a more perfect beast: APP transgenic mice with neuronal loss.构建更完美的“野兽”:伴有神经元缺失的APP转基因小鼠
Am J Pathol. 2004 Apr;164(4):1143-6. doi: 10.1016/S0002-9440(10)63202-6.
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Gender differences in the amount and deposition of amyloidbeta in APPswe and PS1 double transgenic mice.APPswe和PS1双转基因小鼠中β淀粉样蛋白的含量及沉积的性别差异。
Neurobiol Dis. 2003 Dec;14(3):318-27. doi: 10.1016/j.nbd.2003.08.009.
9
Effects of estrogen and raloxifene on neuroglia number and morphology in the hippocampus of aged female mice.雌激素和雷洛昔芬对老年雌性小鼠海马区神经胶质细胞数量和形态的影响。
Neuroscience. 2003;121(3):659-66. doi: 10.1016/s0306-4522(03)00245-8.
10
Behavioral and neurochemical characterization of transgenic mice carrying the human presenilin-1 gene with or without the leucine-to-proline mutation at codon 235.携带人类早老素-1基因且密码子235处有或无亮氨酸到脯氨酸突变的转基因小鼠的行为和神经化学特征
Exp Neurol. 2003 Oct;183(2):673-81. doi: 10.1016/s0014-4886(03)00242-5.

老年雌性双转基因APP/PS1小鼠蓝斑中儿茶酚胺能神经元损失

Catecholaminergic neuronal loss in locus coeruleus of aged female dtg APP/PS1 mice.

作者信息

O'Neil Jahn N, Mouton Peter R, Tizabi Yousef, Ottinger Mary Ann, Lei De-Liang, Ingram Donald K, Manaye Kebreten F

机构信息

Department of Physiology & Biophysics, College of Medicine, Howard University, Washington, DC 20059, United States.

出版信息

J Chem Neuroanat. 2007 Nov;34(3-4):102-7. doi: 10.1016/j.jchemneu.2007.05.008. Epub 2007 May 31.

DOI:10.1016/j.jchemneu.2007.05.008
PMID:17658239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5483173/
Abstract

Alzheimer's disease (AD) is the most common type of dementia afflicting the elderly. In addition to the presence of cortical senile plaques and neurofibrillary tangles, AD is characterized at autopsy by extensive degeneration of brainstem locus coeruleus (LC) neurons that provide noradrenergic innervation to cortical neuropil, together with relative stability of dopaminergic neuron number in substantia nigra (SN) and ventral tegmental area (VTA). The present study used design-based stereological methods to assess catecholaminergic neuronal loss in brains of double transgenic female mice that co-express two human mutations associated with familial AD, amyloid precursor protein (APP(swe)) and presenilin-1 (PS1(DeltaE9)). Mice were analyzed at two age groups, 3-6 months and 16-23 months, when deposition of AD-type beta-amyloid (Abeta) plaques occurs in cortical brain regions. Blocks of brain tissue containing the noradrenergic LC nucleus and two nuclei of dopaminergic neurons, the SN and VTA, were sectioned and sampled in a systematic-random manner and immunostained for tyrosine hydroxylase (TH), a specific marker for catecholaminergic neurons. Using the optical fractionator method we found a 24% reduction in the total number of TH-positive neurons in LC with no changes in SN-VTA of aged dtg APP/PS1 mice compared with non-transgenic controls. No significant differences were observed in numbers of TH-positive neurons in LC or SN-VTA in brains of young female dtg APP/PS1 mice compared to their age-matched controls. The findings of selective neurodegeneration of LC neurons in the brains of aged female dtg APP/PS1 mice mimic the neuropathology in the brains of AD patients at autopsy. These findings support the use of murine models of Abeta deposition to develop novel strategies for the therapeutic management of patients afflicted with AD.

摘要

阿尔茨海默病(AD)是困扰老年人的最常见的痴呆类型。除了存在皮质老年斑和神经原纤维缠结外,AD在尸检时的特征是脑干蓝斑(LC)神经元广泛退化,这些神经元为皮质神经毡提供去甲肾上腺素能神经支配,同时黑质(SN)和腹侧被盖区(VTA)中的多巴胺能神经元数量相对稳定。本研究使用基于设计的立体学方法,评估共表达与家族性AD相关的两个人类突变——淀粉样前体蛋白(APP(swe))和早老素-1(PS1(DeltaE9))的双转基因雌性小鼠大脑中儿茶酚胺能神经元的损失。在两个年龄组对小鼠进行分析,即3 - 6个月和16 - 23个月,此时AD型β-淀粉样蛋白(Aβ)斑块在大脑皮质区域沉积。包含去甲肾上腺素能LC核以及多巴胺能神经元的两个核(SN和VTA)的脑组织块被系统随机切片和取样,并对酪氨酸羟化酶(TH)进行免疫染色,TH是儿茶酚胺能神经元的特异性标志物。使用光学分割法,我们发现与非转基因对照相比,老年双转基因APP/PS1小鼠的LC中TH阳性神经元总数减少了24%,而SN - VTA没有变化。与年龄匹配的对照相比,年轻雌性双转基因APP/PS1小鼠大脑中LC或SN - VTA的TH阳性神经元数量没有显著差异。老年雌性双转基因APP/PS1小鼠大脑中LC神经元选择性神经变性的发现,与AD患者尸检时大脑的神经病理学相似。这些发现支持使用Aβ沉积的小鼠模型来开发治疗AD患者的新策略。

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