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本文引用的文献

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Mechanisms of action of non-steroidal anti-inflammatory drugs for the prevention of Alzheimer's disease.非甾体抗炎药预防阿尔茨海默病的作用机制。
CNS Neurol Disord Drug Targets. 2010 Apr;9(2):140-8. doi: 10.2174/187152710791011991.
2
Sertraline for the treatment of depression in Alzheimer disease.舍曲林治疗阿尔茨海默病中的抑郁症。
Am J Geriatr Psychiatry. 2010 Feb;18(2):136-45. doi: 10.1097/JGP.0b013e3181c796eb.
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Oxidative stress in the progression of Alzheimer disease in the frontal cortex.阿尔茨海默病患者额叶皮质病变过程中的氧化应激。
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Increased iron and free radical generation in preclinical Alzheimer disease and mild cognitive impairment.临床前阿尔茨海默病和轻度认知障碍中铁的增加和自由基的产生。
J Alzheimers Dis. 2010;19(1):363-72. doi: 10.3233/JAD-2010-1239.
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Review: cell cycle aberrations and neurodegeneration.综述:细胞周期异常与神经退行性变。
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Intraneuronal amyloid beta accumulation and oxidative damage to nucleic acids in Alzheimer disease.阿尔茨海默病患者神经元内淀粉样β的积累及核酸的氧化损伤。
Neurobiol Dis. 2010 Mar;37(3):731-7. doi: 10.1016/j.nbd.2009.12.012. Epub 2009 Dec 23.
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Evidence for the progression through S-phase in the ectopic cell cycle re-entry of neurons in Alzheimer disease.阿尔茨海默病中神经元异位细胞周期重新进入时S期进程的证据。
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Promising strategies for the prevention of dementia.预防痴呆症的有前景的策略。
Arch Neurol. 2009 Oct;66(10):1210-5. doi: 10.1001/archneurol.2009.201.
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Abnormal mitochondrial dynamics and neurodegenerative diseases.异常的线粒体动力学与神经退行性疾病。
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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.

阿尔茨海默病治疗的前沿。

Frontiers in Alzheimer's disease therapeutics.

机构信息

Department of Pathology, Case Western Reserve University, Cleveland, Ohio, USA.

出版信息

Ther Adv Chronic Dis. 2011 Jan 1;2(1):9-23. doi: 10.1177/2040622310382817.

DOI:10.1177/2040622310382817
PMID:21743833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3129861/
Abstract

Alzheimer disease (AD) is a progressive neurodegenerative disease which begins with insidious deterioration of higher cognition and progresses to severe dementia. Clinical symptoms typically involve impairment of memory and at least one other cognitive domain. Because of the exponential increase in the incidence of AD with age, the aging population across the world has seen a congruous increase AD, emphasizing the importance of disease altering therapy. Current therapeutics on the market, including cholinesterase inhibitors and N-methyl-D-aspartate receptor antagonists, provide symptomatic relief but do not alter progression of the disease. Therefore, progress in the areas of prevention and disease modification may be of critical interest. In this review, we summarize novel AD therapeutics that are currently being explored, and also mechanisms of action of specific drugs within the context of current knowledge of AD pathologic pathways.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,始于高级认知功能的隐匿性恶化,并进展为严重痴呆。临床症状通常包括记忆障碍和至少其他一个认知领域的损害。由于 AD 的发病率随年龄呈指数增长,全球老龄化人口中 AD 的发病率相应增加,这强调了改变疾病治疗方法的重要性。目前市场上的治疗方法,包括胆碱酯酶抑制剂和 N-甲基-D-天冬氨酸受体拮抗剂,仅能提供症状缓解,而不能改变疾病的进展。因此,预防和疾病修饰领域的进展可能具有重要意义。在这篇综述中,我们总结了目前正在探索的新型 AD 治疗方法,并根据 AD 病理途径的现有知识,总结了特定药物的作用机制。