Multifunctional Fluorescent Probes Unveiling Complex Pathways in Alzheimer’s Disease Pathogenesis

IF 14 Q1 CHEMISTRY, MULTIDISCIPLINARY Accounts of materials research Pub Date : 2024-12-03 DOI:10.1021/accountsmr.4c00303
Priyam Ghosh, Parameswar Krishnan Iyer
{"title":"Multifunctional Fluorescent Probes Unveiling Complex Pathways in Alzheimer’s Disease Pathogenesis","authors":"Priyam Ghosh, Parameswar Krishnan Iyer","doi":"10.1021/accountsmr.4c00303","DOIUrl":null,"url":null,"abstract":"Alzheimer’s disease (AD) is a complex neurological disorder with a progressive nature, posing challenges in diagnosis and treatment. It is characterized by the formation of Aβ plaques and neurofibrillary tangles (NFTs), which have been the focus of clinical diagnosis and treatment. Despite decades of research, the elusive nature of AD has made it difficult to develop widely recognized diagnostic and treatment methods. However, recent advances have led to new diagnostic and therapeutic techniques targeting Aβ and tau. These technologies aim to address gaps in our understanding by targeting biomarkers using multifunctional fluorescent organic-molecule-based theranostics. There is a leading hypothesis that Aβ and its oligomers are crucial pathogenic features in AD-afflicted brains. Metals found in Aβ plaques have been linked to AD, contributing to oxidative stress and stabilizing toxic Aβ oligomers. Drug research is addressing AD’s diverse toxicity, including protein aggregation, metal toxicity, oxidative stress, mitochondrial damage, and neuroinflammation. Drug development is adopting multifaceted approaches, focusing on the intricate interaction of AD contributors. Diverse diagnostic techniques and innovative drug development tactics are crucial for AD diagnosis and therapy advances.","PeriodicalId":72040,"journal":{"name":"Accounts of materials research","volume":"214 1","pages":""},"PeriodicalIF":14.0000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Accounts of materials research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/accountsmr.4c00303","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Alzheimer’s disease (AD) is a complex neurological disorder with a progressive nature, posing challenges in diagnosis and treatment. It is characterized by the formation of Aβ plaques and neurofibrillary tangles (NFTs), which have been the focus of clinical diagnosis and treatment. Despite decades of research, the elusive nature of AD has made it difficult to develop widely recognized diagnostic and treatment methods. However, recent advances have led to new diagnostic and therapeutic techniques targeting Aβ and tau. These technologies aim to address gaps in our understanding by targeting biomarkers using multifunctional fluorescent organic-molecule-based theranostics. There is a leading hypothesis that Aβ and its oligomers are crucial pathogenic features in AD-afflicted brains. Metals found in Aβ plaques have been linked to AD, contributing to oxidative stress and stabilizing toxic Aβ oligomers. Drug research is addressing AD’s diverse toxicity, including protein aggregation, metal toxicity, oxidative stress, mitochondrial damage, and neuroinflammation. Drug development is adopting multifaceted approaches, focusing on the intricate interaction of AD contributors. Diverse diagnostic techniques and innovative drug development tactics are crucial for AD diagnosis and therapy advances.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
揭示阿尔茨海默病发病机制复杂途径的多功能荧光探针
阿尔茨海默病(AD)是一种复杂的进行性神经系统疾病,在诊断和治疗方面都具有挑战性。其特点是形成β斑块和神经原纤维缠结(nft),一直是临床诊断和治疗的重点。尽管经过了几十年的研究,但阿尔茨海默病难以捉摸的性质使得很难开发出广泛认可的诊断和治疗方法。然而,最近的进展已经导致了针对Aβ和tau的新的诊断和治疗技术。这些技术旨在通过使用多功能荧光有机分子为基础的治疗方法靶向生物标志物来解决我们在理解上的差距。有一个主要的假设是,a β及其低聚物是ad患者大脑的关键致病特征。在Aβ斑块中发现的金属与AD有关,有助于氧化应激和稳定有毒的Aβ低聚物。药物研究正在研究阿尔茨海默病的多种毒性,包括蛋白质聚集、金属毒性、氧化应激、线粒体损伤和神经炎症。药物开发正在采用多方面的方法,重点关注阿尔茨海默病致病因子之间复杂的相互作用。多样化的诊断技术和创新的药物开发策略对阿尔茨海默病的诊断和治疗进展至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
17.70
自引率
0.00%
发文量
0
期刊最新文献
Thermoresponsive Hydrogels for the Construction of Smart Windows, Sensors, and Actuators Perspectives of Flexible Thermoelectric Fibers by Thermal Drawing Techniques Constructing High-Performance Heterogeneous Catalysts through Interface Engineering on Metal–Organic Framework Platforms Block Copolymer Based Porous Carbon Fiber─Synthesis, Processing, and Applications Why and How to Investigate Biological Materials Processing: A Cross-Disciplinary Approach for Inspiring Sustainable Materials Fabrication
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1