• 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

阿尔茨海默病的治疗现状和新策略。

Current therapies and new strategies for the management of Alzheimer's disease.

机构信息

The Pharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Rensselaer, NY 12144, USA.

出版信息

Am J Alzheimers Dis Other Demen. 2010 Aug;25(5):414-24. doi: 10.1177/1533317510372372. Epub 2010 Jul 2.

DOI:10.1177/1533317510372372
PMID:20601643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10845420/
Abstract

Alzheimer's disease (AD) is a devastating neurodegenerative disorder that currently affects millions of Americans. There is no cure at present and no real long-term hope for patients with AD. While partially effective in improving symptoms, currently available treatments approved by the US Food and Drug Administration (FDA) do not halt progression of AD, or address the underlying mechanism of the disease, in part because the etiology of AD is still an active area of investigation. Identification of risk factors and the pathogenic mechanism of AD hold the promise of bringing forth novel treatments and perhaps even a cure. In this review, we will summarize some of the risk factors for AD, AD diagnosis, and current treatments. Novel therapeutic strategies such as inhibition of beta-amyloid peptide (Abeta), tau-mediated pathogenesis, and receptors for advanced glycation end products (RAGE), as well as neuroprotective and anti-inflammatory approaches and the impact of cholesterol-lowering, botanical, and nutritional agents are also reviewed.

摘要

阿尔茨海默病(AD)是一种破坏性的神经退行性疾病,目前影响着数以百万计的美国人。目前尚无治愈方法,AD 患者也没有真正的长期希望。虽然部分有效改善症状,但目前美国食品和药物管理局(FDA)批准的可用治疗方法并不能阻止 AD 的进展,也不能解决疾病的根本机制,部分原因是 AD 的病因仍然是一个活跃的研究领域。确定 AD 的风险因素和发病机制有望带来新的治疗方法,甚至可能治愈。在这篇综述中,我们将总结 AD 的一些风险因素、AD 的诊断和当前的治疗方法。还回顾了新型治疗策略,如抑制β-淀粉样肽(Abeta)、tau 介导的发病机制和晚期糖基化终产物受体(RAGE),以及神经保护和抗炎方法,以及降低胆固醇、植物和营养剂的影响。

相似文献

1
Current therapies and new strategies for the management of Alzheimer's disease.阿尔茨海默病的治疗现状和新策略。
Am J Alzheimers Dis Other Demen. 2010 Aug;25(5):414-24. doi: 10.1177/1533317510372372. Epub 2010 Jul 2.
2
Progress in the development of new drugs in Alzheimer's disease.阿尔茨海默病新药研发进展。
J Nutr Health Aging. 2011 Jan;15(1):45-57. doi: 10.1007/s12603-011-0012-x.
3
A review on ferulic acid and analogs based scaffolds for the management of Alzheimer's disease.阿魏酸及其类似物基于支架治疗阿尔茨海默病的研究进展。
Eur J Med Chem. 2021 Apr 5;215:113278. doi: 10.1016/j.ejmech.2021.113278. Epub 2021 Feb 15.
4
Beneficial Effects of Fingolimod in Alzheimer's Disease: Molecular Mechanisms and Therapeutic Potential.芬戈莫德在阿尔茨海默病中的有益作用:分子机制和治疗潜力。
Neuromolecular Med. 2019 Sep;21(3):227-238. doi: 10.1007/s12017-019-08558-2. Epub 2019 Jul 16.
5
An update on treatment and prevention strategies for Alzheimer's disease.阿尔茨海默病治疗与预防策略的最新进展。
Curr Neurol Neurosci Rep. 2009 Sep;9(5):368-76. doi: 10.1007/s11910-009-0054-1.
6
Role of natural products for the treatment of Alzheimer's disease.天然产物在治疗阿尔茨海默病中的作用。
Eur J Pharmacol. 2021 May 5;898:173974. doi: 10.1016/j.ejphar.2021.173974. Epub 2021 Feb 27.
7
Pinocembrin protects against β-amyloid-induced toxicity in neurons through inhibiting receptor for advanced glycation end products (RAGE)-independent signaling pathways and regulating mitochondrion-mediated apoptosis.白杨素通过抑制晚期糖基化终产物受体(RAGE)非依赖性信号通路和调节线粒体介导的细胞凋亡来保护神经元免受β-淀粉样蛋白诱导的毒性。
BMC Med. 2012 Sep 18;10:105. doi: 10.1186/1741-7015-10-105.
8
Therapeutic potentials of plant iridoids in Alzheimer's and Parkinson's diseases: A review.植物环烯醚萜类化合物在阿尔茨海默病和帕金森病中的治疗潜力:综述。
Eur J Med Chem. 2019 May 1;169:185-199. doi: 10.1016/j.ejmech.2019.03.009. Epub 2019 Mar 8.
9
Mechanistic Insight into the Design of Chemical Tools to Control Multiple Pathogenic Features in Alzheimer's Disease.深入了解化学工具设计的机制,以控制阿尔茨海默病中的多种致病特征。
Acc Chem Res. 2021 Oct 19;54(20):3930-3940. doi: 10.1021/acs.accounts.1c00457. Epub 2021 Oct 4.
10
Advances in Alzheimer's disease drug development.阿尔茨海默病药物研发进展。
BMC Med. 2015 Mar 25;13:62. doi: 10.1186/s12916-015-0297-4.

引用本文的文献

1
Adherence to the Mediterranean Diet Is not Related to Beta-Amyloid Deposition: Data from the Women's Healthy Ageing Project.坚持地中海饮食与β-淀粉样蛋白沉积无关:来自妇女健康老龄化项目的数据。
J Prev Alzheimers Dis. 2018;5(2):137-141. doi: 10.14283/jpad.2018.12.
2
Nature Versus Nurture: Does Proteostasis Imbalance Underlie the Genetic, Environmental, and Age-Related Risk Factors for Alzheimer's Disease?先天与后天:蛋白质稳态失衡是否为阿尔茨海默病的遗传、环境及年龄相关风险因素的潜在原因?
Healthcare (Basel). 2017 Aug 22;5(3):46. doi: 10.3390/healthcare5030046.
3
Effects of spaced retrieval training with errorless learning in the rehabilitation of patients with dementia.间隔检索训练结合无错误学习在痴呆患者康复中的作用。
J Phys Ther Sci. 2015 Sep;27(9):2735-8. doi: 10.1589/jpts.27.2735. Epub 2015 Sep 30.
4
High-mobility group box-1 protein and β-amyloid oligomers promote neuronal differentiation of adult hippocampal neural progenitors via receptor for advanced glycation end products/nuclear factor-κB axis: relevance for Alzheimer's disease.高迁移率族蛋白 B1 与β-淀粉样寡聚体通过晚期糖基化终产物受体/核因子-κB 通路促进成年海马神经前体细胞的神经元分化:与阿尔茨海默病的相关性。
J Neurosci. 2013 Apr 3;33(14):6047-59. doi: 10.1523/JNEUROSCI.2052-12.2013.
5
Cryptotanshinione inhibits β-amyloid aggregation and protects damage from β-amyloid in SH-SY5Y cells.隐丹参酮抑制β-淀粉样蛋白聚集,并保护 SH-SY5Y 细胞免受β-淀粉样蛋白的损伤。
Neurochem Res. 2012 Mar;37(3):622-8. doi: 10.1007/s11064-011-0652-6. Epub 2011 Nov 19.
6
Therapeutic potential and anti-amyloidosis mechanisms of tert-butylhydroquinone for Alzheimer's disease.特丁基对苯二酚治疗阿尔茨海默病的潜力及抗淀粉样变性机制。
J Alzheimers Dis. 2011;26(4):767-78. doi: 10.3233/JAD-2011-110512.

本文引用的文献

1
Biomarkers for Alzheimer's disease and other forms of dementia: clinical needs, limitations and future aspects.阿尔茨海默病和其他形式痴呆症的生物标志物:临床需求、局限性和未来方面。
Exp Gerontol. 2010 Jan;45(1):5-14. doi: 10.1016/j.exger.2009.09.008. Epub 2009 Sep 29.
2
Advances in tau-focused drug discovery for Alzheimer's disease and related tauopathies.针对阿尔茨海默病及相关tau蛋白病的tau靶向药物研发进展。
Nat Rev Drug Discov. 2009 Oct;8(10):783-93. doi: 10.1038/nrd2959.
3
Imaging and biomarkers in early Alzheimer's disease and mild cognitive impairment.早期阿尔茨海默病和轻度认知障碍中的影像学与生物标志物
Clin Pharmacol Ther. 2009 Oct;86(4):438-41. doi: 10.1038/clpt.2009.166. Epub 2009 Aug 26.
4
Baseline MRI predictors of conversion from MCI to probable AD in the ADNI cohort.阿尔茨海默病神经成像计划(ADNI)队列中从轻度认知障碍(MCI)转变为可能的阿尔茨海默病(AD)的基线磁共振成像(MRI)预测指标。
Curr Alzheimer Res. 2009 Aug;6(4):347-61. doi: 10.2174/156720509788929273.
5
Pyrano[3,2-c]quinoline-6-chlorotacrine hybrids as a novel family of acetylcholinesterase- and beta-amyloid-directed anti-Alzheimer compounds.吡喃并[3,2-c]喹啉-6-氯他克林杂合物作为一类新型的乙酰胆碱酯酶和β-淀粉样蛋白导向的抗阿尔茨海默病化合物。
J Med Chem. 2009 Sep 10;52(17):5365-79. doi: 10.1021/jm900859q.
6
MRI and CSF biomarkers in normal, MCI, and AD subjects: predicting future clinical change.正常、轻度认知障碍和阿尔茨海默病患者的MRI及脑脊液生物标志物:预测未来临床变化
Neurology. 2009 Jul 28;73(4):294-301. doi: 10.1212/WNL.0b013e3181af79fb.
7
MRI and CSF biomarkers in normal, MCI, and AD subjects: diagnostic discrimination and cognitive correlations.正常、轻度认知障碍和阿尔茨海默病受试者的MRI和脑脊液生物标志物:诊断鉴别及认知相关性
Neurology. 2009 Jul 28;73(4):287-93. doi: 10.1212/WNL.0b013e3181af79e5.
8
Alzheimer's Disease in Adults with Down Syndrome.唐氏综合征成年患者中的阿尔茨海默病
Int Rev Res Ment Retard. 2008 Jan 1;36:103-145. doi: 10.1016/S0074-7750(08)00004-9.
9
Drug development for Alzheimer's disease: where are we now and where are we headed?阿尔茨海默病的药物研发:我们现在何处,又将走向何方?
Am J Geriatr Pharmacother. 2009 Jun;7(3):167-85. doi: 10.1016/j.amjopharm.2009.06.003.
10
Neprilysin and insulin-degrading enzyme levels are increased in Alzheimer disease in relation to disease severity.在阿尔茨海默病中,中性内肽酶和胰岛素降解酶水平随疾病严重程度增加。
J Neuropathol Exp Neurol. 2009 Aug;68(8):902-14. doi: 10.1097/NEN.0b013e3181afe475.