• 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

阿尔茨海默病及其他淀粉样变性的侵入性和非侵入性治疗方法。

Invasive and non-invasive therapies for Alzheimer's disease and other amyloidosis.

作者信息

Pandey Gaurav, Ramakrishnan Vibin

机构信息

Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, 781039, India.

出版信息

Biophys Rev. 2020 Oct;12(5):1175-1186. doi: 10.1007/s12551-020-00752-y. Epub 2020 Sep 15.

DOI:10.1007/s12551-020-00752-y
PMID:32930962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7575678/
Abstract

Advancements in medical science have facilitated in extending human lives. The increased life expectancy, though, has come at a cost. The cases of an aging population suffering from degenerative diseases like Alzheimer's disease (AD) are presently at its all-time high. Amyloidosis disorders such as AD are triggered by an abnormal transition of soluble proteins into their highly ordered aggregated forms. The landscape of amyloidosis treatment remains unchanged, and there is no cure for such disorders. However, an increased understanding of the mechanism of amyloid self-assembly has given hope for a possible therapeutic solution. In this review, we will discuss the current state of molecular and non-molecular options for therapeutic intervention of amyloidosis. We highlight the efficacy of non-invasive physical therapies as possible alternatives to their molecular counterparts. Graphical abstract.

摘要

医学科学的进步有助于延长人类寿命。然而,预期寿命的增加是有代价的。目前,患有阿尔茨海默病(AD)等退行性疾病的老年人口数量达到了历史最高水平。诸如AD之类的淀粉样变性疾病是由可溶性蛋白质异常转变为高度有序的聚集形式引发的。淀粉样变性疾病的治疗现状没有改变,此类疾病无法治愈。然而,对淀粉样蛋白自组装机制的深入了解为可能的治疗方案带来了希望。在本综述中,我们将讨论淀粉样变性疾病治疗干预的分子和非分子选择的现状。我们强调非侵入性物理疗法作为分子疗法替代方案的有效性。图形摘要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a44c/7575678/3a8f446eda21/12551_2020_752_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a44c/7575678/3a8f446eda21/12551_2020_752_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a44c/7575678/3a8f446eda21/12551_2020_752_Figa_HTML.jpg

相似文献

1
Invasive and non-invasive therapies for Alzheimer's disease and other amyloidosis.阿尔茨海默病及其他淀粉样变性的侵入性和非侵入性治疗方法。
Biophys Rev. 2020 Oct;12(5):1175-1186. doi: 10.1007/s12551-020-00752-y. Epub 2020 Sep 15.
2
A mechanistic survey of Alzheimer's disease.阿尔茨海默病的机制研究
Biophys Chem. 2022 Feb;281:106735. doi: 10.1016/j.bpc.2021.106735. Epub 2021 Nov 30.
3
Aβ and Tau Interact with Metal Ions, Lipid Membranes and Peptide-Based Amyloid Inhibitors: Are These Common Features Relevant in Alzheimer's Disease?β淀粉样蛋白和 Tau 与金属离子、脂膜和基于肽的淀粉样蛋白抑制剂相互作用:这些共同特征在阿尔茨海默病中是否相关?
Molecules. 2022 Aug 9;27(16):5066. doi: 10.3390/molecules27165066.
4
Protein misfolding, aggregation and mechanism of amyloid cytotoxicity: An overview and therapeutic strategies to inhibit aggregation.蛋白质错误折叠、聚集和淀粉样细胞毒性的机制:概述和抑制聚集的治疗策略。
Int J Biol Macromol. 2019 Aug 1;134:1022-1037. doi: 10.1016/j.ijbiomac.2019.05.109. Epub 2019 May 22.
5
[Can prion-like propagation occur in neurodegenerative diseases?: in view of transmissible systemic amyloidosis].[朊病毒样传播会在神经退行性疾病中发生吗?:鉴于可传播的系统性淀粉样变性]
Brain Nerve. 2012 Jun;64(6):665-74.
6
An Insight into the Protein Aggregation in Alzheimer's Disease and its Inhibition.深入了解阿尔茨海默病中的蛋白质聚集及其抑制作用。
Protein Pept Lett. 2023;30(11):900-912. doi: 10.2174/0109298665247757231020044633.
7
Process, Outcomes and Possible Elimination of Aggregation with Special Reference to Heme Proteins; Likely Remediations of Proteinopathies.过程、结果和聚集的可能消除,特别参考血红素蛋白;蛋白构象病的可能修复。
Curr Protein Pept Sci. 2020;21(6):573-583. doi: 10.2174/1389203721666200204122732.
8
Cross-Linking Mass Spectrometry Analysis of Metastable Compact Structures in Intrinsically Disordered Proteins.交联质谱分析无序蛋白质中亚稳态致密结构。
Methods Mol Biol. 2023;2551:189-201. doi: 10.1007/978-1-0716-2597-2_13.
9
Alzheimer's disease, beta-amyloidosis, and aging.阿尔茨海默病、β-淀粉样变性与衰老。
Rev Neurosci. 1994 Oct-Dec;5(4):275-92. doi: 10.1515/revneuro.1994.5.4.275.
10
Molecular and clinical insights into protein misfolding and associated amyloidosis.蛋白质错误折叠与相关淀粉样变性的分子与临床研究进展
Eur J Med Chem. 2019 Dec 15;184:111753. doi: 10.1016/j.ejmech.2019.111753. Epub 2019 Oct 7.

引用本文的文献

1
Unraveling APOE4's Role in Alzheimer's Disease: Pathologies and Therapeutic Strategies.解析载脂蛋白E4在阿尔茨海默病中的作用:病理与治疗策略
Curr Protein Pept Sci. 2025;26(4):259-281. doi: 10.2174/0113892037326839241014054430.
2
CRISPR/Cas9 Gene Editing: A Novel Approach Towards Alzheimer's Disease Treatment.CRISPR/Cas9 基因编辑:治疗阿尔茨海默病的新方法。
CNS Neurol Disord Drug Targets. 2024;23(12):1405-1424. doi: 10.2174/0118715273283786240408034408.
3
Revolutionizing the Early Detection of Alzheimer's Disease through Non-Invasive Biomarkers: The Role of Artificial Intelligence and Deep Learning.

本文引用的文献

1
Modulation of aggregation with an electric field; scientific roadmap for a potential non-invasive therapy against tauopathies.电场对聚集的调节;针对tau蛋白病的潜在非侵入性治疗的科学路线图。
RSC Adv. 2019 Feb 6;9(9):4744-4750. doi: 10.1039/c8ra09993f. eCollection 2019 Feb 5.
2
Modulation of tau protein aggregation using 'Trojan' sequences.利用“木马”序列调节 tau 蛋白聚集。
Biochim Biophys Acta Gen Subj. 2020 Jul;1864(7):129569. doi: 10.1016/j.bbagen.2020.129569. Epub 2020 Feb 27.
3
Recent advances in the design and applications of amyloid-β peptide aggregation inhibitors for Alzheimer's disease therapy.
通过非侵入性生物标志物实现阿尔茨海默病的早期检测的革命:人工智能和深度学习的作用。
Sensors (Basel). 2023 Apr 22;23(9):4184. doi: 10.3390/s23094184.
4
Efficient Biosorption of Hexavalent Chromium from Water with Human Hair.人发对水中六价铬的高效生物吸附
ACS Omega. 2022 Dec 20;8(1):915-924. doi: 10.1021/acsomega.2c06268. eCollection 2023 Jan 10.
5
Therapeutic non-invasive brain treatments in Alzheimer's disease: recent advances and challenges.阿尔茨海默病的治疗性非侵入性脑治疗:最新进展与挑战
Inflamm Regen. 2022 Oct 3;42(1):31. doi: 10.1186/s41232-022-00216-8.
6
CRISPR/Cas9 gene editing: New hope for Alzheimer's disease therapeutics.CRISPR/Cas9 基因编辑:阿尔茨海默病治疗的新希望。
J Adv Res. 2022 Sep;40:207-221. doi: 10.1016/j.jare.2021.07.001. Epub 2021 Jul 6.
7
Biophysical Reviews: a Q1 ranked journal in biophysics and structural biology.《生物物理评论》:生物物理学和结构生物学领域排名第一季度的期刊。
Biophys Rev. 2020 Oct;12(5):1085-1089. doi: 10.1007/s12551-020-00764-8. Epub 2020 Sep 29.
用于阿尔茨海默病治疗的淀粉样β肽聚集抑制剂的设计与应用的最新进展。
Biophys Rev. 2019 Nov 12. doi: 10.1007/s12551-019-00606-2.
4
Peptide-/Drug-Directed Self-Assembly of Hybrid Polyurethane Hydrogels for Wound Healing.肽/药物导向的杂化聚氨酯水凝胶用于伤口愈合的自组装。
ACS Appl Mater Interfaces. 2019 Oct 9;11(40):37147-37155. doi: 10.1021/acsami.9b13708. Epub 2019 Sep 24.
5
Mimicking Molecular Chaperones to Regulate Protein Folding.模拟分子伴侣调节蛋白质折叠。
Adv Mater. 2020 Jan;32(3):e1805945. doi: 10.1002/adma.201805945. Epub 2019 May 2.
6
Therapeutic noninvasive brain stimulation in Alzheimer's disease and related dementias.阿尔茨海默病及相关痴呆的治疗性无创脑刺激。
Curr Opin Neurol. 2019 Apr;32(2):292-304. doi: 10.1097/WCO.0000000000000669.
7
Electric Field Disruption of Amyloid Aggregation: Potential Noninvasive Therapy for Alzheimer's Disease.电场干扰淀粉样蛋白聚集:阿尔茨海默病的潜在非侵入性治疗方法。
ACS Chem Neurosci. 2019 May 15;10(5):2250-2262. doi: 10.1021/acschemneuro.8b00490. Epub 2019 Feb 15.
8
Status of Noninvasive Brain Stimulation in the Therapy of Alzheimer's Disease.非侵入性脑刺激在阿尔茨海默病治疗中的现状
Chin Med J (Engl). 2018 Dec 20;131(24):2899-2903. doi: 10.4103/0366-6999.247217.
9
The search for better animal models of Alzheimer's disease.寻找更好的阿尔茨海默病动物模型。
Nature. 2018 Jul;559(7715):S13-S15. doi: 10.1038/d41586-018-05722-9.
10
Modeling Alzheimer's disease brains in vitro.体外模拟阿尔茨海默病大脑。
Nat Neurosci. 2018 Jul;21(7):899-900. doi: 10.1038/s41593-018-0177-2.