• 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

阿尔茨海默病:细胞与药理学方面

Alzheimer's Disease: Cellular and Pharmacological Aspects.

作者信息

Aranda-Abreu Gonzalo Emiliano, Rojas-Durán Fausto, Hernández-Aguilar María Elena, Herrera-Covarrubias Deissy, Chí-Castañeda Lizbeth Donají, Toledo-Cárdenas María Rebeca, Suárez-Medellín Jorge Manuel

机构信息

Instituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa 91192, Mexico.

出版信息

Geriatrics (Basel). 2024 Jun 22;9(4):86. doi: 10.3390/geriatrics9040086.

DOI:10.3390/geriatrics9040086
PMID:39051250
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11270425/
Abstract

Alzheimer's disease was described more than 100 years ago and despite the fact that several molecules are being tested for its treatment, which are in phase III trials, the disease continues to progress. The main problem is that these molecules function properly in healthy neurons, while neuronal pathology includes plasma membrane disruption, malfunction of various organelles, and hyperphosphorylation of Tau and amyloid plaques. The main objective of this article is the discussion of a neuronal restoration therapy, where molecules designed for the treatment of Alzheimer's disease would probably be more effective, and the quality of life of people would be better.

摘要

阿尔茨海默病在100多年前就有记载,尽管目前有几种分子正在进行治疗该疾病的III期试验,但病情仍在进展。主要问题在于这些分子在健康神经元中能正常发挥作用,而神经元病理包括质膜破坏、各种细胞器功能异常以及Tau蛋白过度磷酸化和淀粉样斑块。本文的主要目的是探讨一种神经元修复疗法,针对阿尔茨海默病设计的分子可能在此疗法中更有效,进而改善患者的生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad8/11270425/8e93ab577ac3/geriatrics-09-00086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad8/11270425/6588ecf4ca1d/geriatrics-09-00086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad8/11270425/8e93ab577ac3/geriatrics-09-00086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad8/11270425/6588ecf4ca1d/geriatrics-09-00086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad8/11270425/8e93ab577ac3/geriatrics-09-00086-g002.jpg

相似文献

1
Alzheimer's Disease: Cellular and Pharmacological Aspects.阿尔茨海默病:细胞与药理学方面
Geriatrics (Basel). 2024 Jun 22;9(4):86. doi: 10.3390/geriatrics9040086.
2
Inositol trisphosphate 3-kinase B is increased in human Alzheimer brain and exacerbates mouse Alzheimer pathology.三磷酸肌醇 3-激酶 B 在人类阿尔茨海默病脑中增加,并加剧了小鼠阿尔茨海默病的病理变化。
Brain. 2014 Feb;137(Pt 2):537-52. doi: 10.1093/brain/awt344. Epub 2014 Jan 8.
3
Alpha1-antichymotrypsin, an inflammatory protein overexpressed in Alzheimer's disease brain, induces tau phosphorylation in neurons.α1-抗糜蛋白酶是一种在阿尔茨海默病大脑中过度表达的炎症蛋白,可诱导神经元中的tau蛋白磷酸化。
Brain. 2006 Nov;129(Pt 11):3020-34. doi: 10.1093/brain/awl255. Epub 2006 Sep 20.
4
Recent therapeutic strategies targeting beta amyloid and tauopathies in Alzheimer's disease.针对阿尔茨海默病中β淀粉样蛋白和tau 病的最新治疗策略。
Brain Res Bull. 2019 Mar;146:171-184. doi: 10.1016/j.brainresbull.2019.01.004. Epub 2019 Jan 8.
5
[Intensive protein synthesis in neurons and phosphorylation of beta-amyloid precursor protein and tau-protein are triggering factors of neuronal amyloidosis and Alzheimer's disease].[神经元中强烈的蛋白质合成以及β-淀粉样前体蛋白和tau蛋白的磷酸化是神经元淀粉样变性和阿尔茨海默病的触发因素]
Biomed Khim. 2013 Mar-Apr;59(2):144-70. doi: 10.18097/pbmc20135902144.
6
Beneficial effect of human anti-amyloid-beta active immunization on neurite morphology and tau pathology.人抗淀粉样蛋白-β主动免疫对神经突形态和 Tau 病理学的有益作用。
Brain. 2010 May;133(Pt 5):1312-27. doi: 10.1093/brain/awq056. Epub 2010 Mar 31.
7
[Pharmacology of Alzheimer's disease: where do we go from here?].[阿尔茨海默病的药理学:我们从这里走向何方?]
Therapie. 2005 Mar-Apr;60(2):89-107. doi: 10.2515/therapie:2005013.
8
Neurons derived from sporadic Alzheimer's disease iPSCs reveal elevated TAU hyperphosphorylation, increased amyloid levels, and GSK3B activation.源自散发性阿尔茨海默病 iPSC 的神经元显示出 TAU 过度磷酸化增加、淀粉样蛋白水平升高和 GSK3β 激活。
Alzheimers Res Ther. 2017 Dec 1;9(1):90. doi: 10.1186/s13195-017-0317-z.
9
Dissecting phenotypic traits linked to human resilience to Alzheimer's pathology.解析与人类对阿尔茨海默病病理的抵抗力相关的表型特征。
Brain. 2013 Aug;136(Pt 8):2510-26. doi: 10.1093/brain/awt171. Epub 2013 Jul 3.
10
Alzheimer-related decrease in CYFIP2 links amyloid production to tau hyperphosphorylation and memory loss.与阿尔茨海默病相关的CYFIP2减少将淀粉样蛋白生成与tau蛋白过度磷酸化及记忆丧失联系起来。
Brain. 2016 Oct;139(Pt 10):2751-2765. doi: 10.1093/brain/aww205. Epub 2016 Aug 14.

本文引用的文献

1
Addressing the Discrepancies Between Animal Models and Human Alzheimer's Disease Pathology: Implications for Translational Research.解决动物模型与人类阿尔茨海默病病理学之间的差异:对转化研究的影响。
J Alzheimers Dis. 2024;98(4):1199-1218. doi: 10.3233/JAD-240058.
2
The Unfolded Protein Response in a Murine Model of Alzheimer's Disease: Looking for Predictors.阿尔茨海默病小鼠模型中的未折叠蛋白反应:寻找预测因子。
Int J Mol Sci. 2023 Nov 11;24(22):16200. doi: 10.3390/ijms242216200.
3
Trial of Solanezumab in Preclinical Alzheimer's Disease.
在临床前阿尔茨海默病中进行的 Solanezumab 试验。
N Engl J Med. 2023 Sep 21;389(12):1096-1107. doi: 10.1056/NEJMoa2305032. Epub 2023 Jul 17.
4
Pathogenesis, Animal Models, and Drug Discovery of Alzheimer's Disease.阿尔茨海默病的发病机制、动物模型和药物发现。
J Alzheimers Dis. 2023;94(4):1265-1301. doi: 10.3233/JAD-230326.
5
Lecanemab in Early Alzheimer's Disease. Reply.用于早期阿尔茨海默病的lecanemab。回复。
N Engl J Med. 2023 Apr 27;388(17):1631-1632. doi: 10.1056/NEJMc2301380.
6
The unfolded protein response transcription factor XBP1s ameliorates Alzheimer's disease by improving synaptic function and proteostasis.未折叠蛋白反应转录因子 XBP1s 通过改善突触功能和蛋白质稳态来缓解阿尔茨海默病。
Mol Ther. 2023 Jul 5;31(7):2240-2256. doi: 10.1016/j.ymthe.2023.03.028. Epub 2023 Apr 4.
7
Vx-809, a CFTR Corrector, Acts through a General Mechanism of Protein Folding and on the Inflammatory Process.Vx-809,一种 CFTR 纠正剂,通过一种蛋白质折叠的通用机制和炎症过程发挥作用。
Int J Mol Sci. 2023 Feb 20;24(4):4252. doi: 10.3390/ijms24044252.
8
Evaluating the Safety and Efficacy of Crenezumab vs Placebo in Adults With Early Alzheimer Disease: Two Phase 3 Randomized Placebo-Controlled Trials.评估 Crenezumab 与安慰剂在早期阿尔茨海默病成人患者中的安全性和疗效:两项 3 期随机安慰剂对照试验。
JAMA Neurol. 2022 Nov 1;79(11):1113-1121. doi: 10.1001/jamaneurol.2022.2909.
9
Metabolic and Cellular Compartments of Acetyl-CoA in the Healthy and Diseased Brain.健康和患病大脑中乙酰辅酶 A 的代谢和细胞区室。
Int J Mol Sci. 2022 Sep 3;23(17):10073. doi: 10.3390/ijms231710073.
10
Aducanumab: Appropriate Use Recommendations Update.阿杜卡奴单抗:合理使用建议更新。
J Prev Alzheimers Dis. 2022;9(2):221-230. doi: 10.14283/jpad.2022.34.