• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[基于APP、MAPT和早老素基因突变的阿尔茨海默病发病机制研究中的选定小鼠模型]

[Selected mice models based on APP, MAPT and presenilin gene mutations in research on the pathogenesis of Alzheimer's disease].

作者信息

Więdłocha Magdalena, Stańczykiewicz Bartłomiej, Jakubik Marta, Rymaszewska Joanna

机构信息

Projekt POIG pn. Innowacyjne technologie produkcji biopreparatów na bazie nowej generacji jaj (OVOCURA).

出版信息

Postepy Hig Med Dosw (Online). 2012 Jun 22;66:415-30. doi: 10.5604/17322693.1001098.

DOI:10.5604/17322693.1001098
PMID:22922141
Abstract

The research conducted on animal models of Alzheimer's disease (AD) has provided valuable information about the pathogenesis of this disease and associated behavioral and cognitive deficits as well as the disease-associated anatomical and histopathological lesions of the brain. Transgenic technologies have enabled the creation of animal models based on mutations in APP, MAPT, presenilin genes, tau protein and apoE. Due to economic reasons studies are mainly conducted on mice. Their brain tissue, depending on the mutation, is characterized by histopathological changes, such as the presence of amyloid plaques, tau protein deposits and dystrophic neurites, gliosis, hippocampal atrophy and amyloid accumulation in vessels. Animal cognitive impairment and behavior, which can be demonstrated in behavioral tests, primarily relate to the working and reference memory, alternation and anxiety. Unfortunately, despite the various modifications specific to AD in the genome of animals, scientists have failed to create an animal model characterized by all the pathological changes that can occur in Alzheimer's disease. Nevertheless, the role of transgenic animals is undeniable, both in research on AD neuropathology and for testing new therapies, such as immunotherapy. Despite the occurrence of abundant Alzheimer's disease mice models this article is dedicated to selected models with mutations in the APP, MAPT and presenilin genes and their application for behavioral studies.

摘要

对阿尔茨海默病(AD)动物模型的研究为该疾病的发病机制、相关行为和认知缺陷以及与疾病相关的大脑解剖和组织病理学病变提供了有价值的信息。转基因技术使得基于APP、MAPT、早老素基因、tau蛋白和载脂蛋白E的突变创建动物模型成为可能。由于经济原因,研究主要在小鼠身上进行。根据突变情况,它们的脑组织具有组织病理学变化特征,如淀粉样斑块、tau蛋白沉积和营养不良性神经突的存在、胶质增生、海马萎缩以及血管中的淀粉样蛋白积累。动物的认知障碍和行为(可在行为测试中表现出来)主要与工作记忆、参考记忆、交替和焦虑有关。不幸的是,尽管动物基因组中有各种特定于AD的修饰,但科学家们仍未能创建出一种具有阿尔茨海默病可能出现的所有病理变化特征的动物模型。然而,转基因动物在AD神经病理学研究和测试新疗法(如免疫疗法)方面的作用是不可否认的。尽管有大量的阿尔茨海默病小鼠模型,但本文致力于研究APP、MAPT和早老素基因突变的选定模型及其在行为研究中的应用。

相似文献

1
[Selected mice models based on APP, MAPT and presenilin gene mutations in research on the pathogenesis of Alzheimer's disease].[基于APP、MAPT和早老素基因突变的阿尔茨海默病发病机制研究中的选定小鼠模型]
Postepy Hig Med Dosw (Online). 2012 Jun 22;66:415-30. doi: 10.5604/17322693.1001098.
2
Modeling Alzheimer's disease in mouse without mutant protein overexpression: cooperative and independent effects of Aβ and tau.在不表达突变蛋白的情况下,用小鼠模拟阿尔茨海默病:Aβ 和 tau 的协同和独立作用。
PLoS One. 2013 Nov 20;8(11):e80706. doi: 10.1371/journal.pone.0080706. eCollection 2013.
3
Progress toward valid transgenic mouse models for Alzheimer's disease.用于阿尔茨海默病的有效转基因小鼠模型的研究进展。
Neurobiol Aging. 1999 Mar-Apr;20(2):201-11. doi: 10.1016/s0197-4580(99)00042-1.
4
Characterisation of cytoskeletal abnormalities in mice transgenic for wild-type human tau and familial Alzheimer's disease mutants of APP and presenilin-1.野生型人类tau蛋白以及淀粉样前体蛋白(APP)和早老素-1(presenilin-1)家族性阿尔茨海默病突变体转基因小鼠细胞骨架异常的特征分析
Neurobiol Dis. 2004 Feb;15(1):47-60. doi: 10.1016/j.nbd.2003.09.007.
5
Long-Term Treatment with Liraglutide, a Glucagon-Like Peptide-1 (GLP-1) Receptor Agonist, Has No Effect on β-Amyloid Plaque Load in Two Transgenic APP/PS1 Mouse Models of Alzheimer's Disease.在两种阿尔茨海默病转基因APP/PS1小鼠模型中,胰高血糖素样肽-1(GLP-1)受体激动剂利拉鲁肽的长期治疗对β淀粉样蛋白斑块负荷无影响。
PLoS One. 2016 Jul 15;11(7):e0158205. doi: 10.1371/journal.pone.0158205. eCollection 2016.
6
Amyloid deposition precedes tangle formation in a triple transgenic model of Alzheimer's disease.在阿尔茨海默病的三重转基因模型中,淀粉样蛋白沉积先于缠结形成。
Neurobiol Aging. 2003 Dec;24(8):1063-70. doi: 10.1016/j.neurobiolaging.2003.08.012.
7
Increase in Tau Pathology in P290S Knock-In Mice Crossed with Mice.P290S 敲入小鼠与 小鼠杂交后 Tau 病理学增加。
eNeuro. 2022 Dec 20;9(6). doi: 10.1523/ENEURO.0247-22.2022. Print 2022 Nov-Dec.
8
Intraneuronal beta-amyloid accumulation in the amygdala enhances fear and anxiety in Alzheimer's disease transgenic mice.杏仁核内的神经元β-淀粉样蛋白积累增强了阿尔茨海默病转基因小鼠的恐惧和焦虑。
Biol Psychiatry. 2010 Mar 15;67(6):513-21. doi: 10.1016/j.biopsych.2009.06.015. Epub 2009 Aug 7.
9
Molecular and functional signatures in a novel Alzheimer's disease mouse model assessed by quantitative proteomics.通过定量蛋白质组学评估新型阿尔茨海默病小鼠模型中的分子和功能特征。
Mol Neurodegener. 2018 Jan 16;13(1):2. doi: 10.1186/s13024-017-0234-4.
10
Chronic gliosis triggers Alzheimer's disease-like processing of amyloid precursor protein.慢性胶质细胞增生引发淀粉样前体蛋白的阿尔茨海默病样加工。
Neuroscience. 2002;113(4):785-96. doi: 10.1016/s0306-4522(02)00230-0.

引用本文的文献

1
Beyond Transgenic Mice: Emerging Models and Translational Strategies in Alzheimer's Disease.超越转基因小鼠:阿尔茨海默病的新兴模型与转化策略
Int J Mol Sci. 2025 Jun 10;26(12):5541. doi: 10.3390/ijms26125541.
2
Compensatory mechanisms in genetic models of neurodegeneration: are the mice better than humans?神经退行性变遗传模型中的代偿机制:老鼠比人类更好吗?
Front Cell Neurosci. 2015 Mar 6;9:56. doi: 10.3389/fncel.2015.00056. eCollection 2015.
3
Early life nutrient restriction impairs blood-brain metabolic profile and neurobehavior predisposing to Alzheimer's disease with aging.
早期生活营养限制会损害血液-大脑代谢特征,并随着年龄的增长导致阿尔茨海默病的神经行为倾向。
Brain Res. 2013 Feb 7;1495:61-75. doi: 10.1016/j.brainres.2012.11.050. Epub 2012 Dec 7.