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Drugs Aging. 2021 May;38(5):407-415. doi: 10.1007/s40266-021-00845-7. Epub 2021 Mar 15.
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Participation of Amyloid and Tau Protein in Post-Ischemic Neurodegeneration of the Hippocampus of a Nature Identical to Alzheimer's Disease.淀粉样蛋白和 Tau 蛋白参与与阿尔茨海默病相似的自然状态下缺血性海马神经退行性变。
Int J Mol Sci. 2021 Feb 28;22(5):2460. doi: 10.3390/ijms22052460.
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Protective effects of antidepressant citalopram against abnormal APP processing and amyloid beta-induced mitochondrial dynamics, biogenesis, mitophagy and synaptic toxicities in Alzheimer's disease.抗抑郁药西酞普兰对阿尔茨海默病中异常 APP 处理及淀粉样β诱导的线粒体动力学、生物发生、线粒体自噬和突触毒性的保护作用。
Hum Mol Genet. 2021 May 29;30(10):847-864. doi: 10.1093/hmg/ddab054.
4
The pleiotropic neuroprotective effects of resveratrol in cognitive decline and Alzheimer's disease pathology: From antioxidant to epigenetic therapy.白藜芦醇在认知能力下降和阿尔茨海默病病理中的多效神经保护作用:从抗氧化剂到表观遗传疗法。
Ageing Res Rev. 2021 May;67:101271. doi: 10.1016/j.arr.2021.101271. Epub 2021 Feb 8.
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New Frontiers in the Prevention, Diagnosis, and Treatment of Alzheimer's Disease.阿尔茨海默病预防、诊断和治疗的新前沿。
J Alzheimers Dis. 2021;82(s1):S51-S63. doi: 10.3233/JAD-201059.
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Intranasal Insulin for Alzheimer's Disease.用于治疗阿尔茨海默病的鼻内胰岛素
CNS Drugs. 2021 Jan;35(1):21-37. doi: 10.1007/s40263-020-00781-x. Epub 2021 Jan 30.
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Intranasal insulin.鼻内胰岛素。
J Neuroendocrinol. 2021 Apr;33(4):e12934. doi: 10.1111/jne.12934. Epub 2021 Jan 28.
8
Myricetin as a Promising Molecule for the Treatment of Post-Ischemic Brain Neurodegeneration.杨梅素作为治疗缺血性脑神经退行性变的有前途的分子。
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Defective Autophagy and Mitophagy in Aging and Alzheimer's Disease.衰老与阿尔茨海默病中的自噬和线粒体自噬缺陷
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一些用于阿尔茨海默病药物治疗的候选药物。

Some Candidate Drugs for Pharmacotherapy of Alzheimer's Disease.

作者信息

Miziak Barbara, Błaszczyk Barbara, Czuczwar Stanisław J

机构信息

Department of Pathophysiology, Medical University of Lublin, 20-090 Lublin, Poland.

Faculty of Health Sciences, High School of Economics, Law and Medical Sciences, 25-734 Kielce, Poland.

出版信息

Pharmaceuticals (Basel). 2021 May 13;14(5):458. doi: 10.3390/ph14050458.

DOI:10.3390/ph14050458
PMID:34068096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8152728/
Abstract

Alzheimer's disease (AD; progressive neurodegenerative disorder) is associated with cognitive and functional impairment with accompanying neuropsychiatric symptoms. The available pharmacological treatment is of a symptomatic nature and, as such, it does not modify the cause of AD. The currently used drugs to enhance cognition include an N-methyl-d-aspartate receptor antagonist (memantine) and cholinesterase inhibitors. The PUBMED, Medical Subject Heading and Clinical Trials databases were used for searching relevant data. Novel treatments are focused on already approved drugs for other conditions and also searching for innovative drugs encompassing investigational compounds. Among the approved drugs, we investigated, are intranasal insulin (and other antidiabetic drugs: liraglitude, pioglitazone and metformin), bexarotene (an anti-cancer drug and a retinoid X receptor agonist) or antidepressant drugs (citalopram, escitalopram, sertraline, mirtazapine). The latter, especially when combined with antipsychotics (for instance quetiapine or risperidone), were shown to reduce neuropsychiatric symptoms in AD patients. The former enhanced cognition. Procognitive effects may be also expected with dietary antioxidative and anti-inflammatory supplements-curcumin, myricetin, and resveratrol. Considering a close relationship between brain ischemia and AD, they may also reduce post-brain ischemia neurodegeneration. An investigational compound, CN-105 (a lipoprotein E agonist), has a very good profile in AD preclinical studies, and its clinical trial for postoperative dementia is starting soon.

摘要

阿尔茨海默病(AD;进行性神经退行性疾病)与认知和功能障碍以及伴随的神经精神症状相关。现有的药物治疗具有对症性质,因此,它并不能改变AD的病因。目前用于增强认知的药物包括N-甲基-D-天冬氨酸受体拮抗剂(美金刚)和胆碱酯酶抑制剂。使用了PUBMED、医学主题词和临床试验数据库来搜索相关数据。新型治疗方法专注于已批准用于其他病症的药物,同时也在寻找包括研究性化合物在内的创新药物。在已批准的药物中,我们研究了鼻内胰岛素(以及其他抗糖尿病药物:利拉鲁肽、吡格列酮和二甲双胍)、贝沙罗汀(一种抗癌药物和视黄酸X受体激动剂)或抗抑郁药物(西酞普兰、艾司西酞普兰、舍曲林、米氮平)。后者,尤其是与抗精神病药物(如喹硫平或利培酮)联合使用时,已被证明可减轻AD患者的神经精神症状。前者可增强认知。饮食中的抗氧化和抗炎补充剂——姜黄素、杨梅素和白藜芦醇也可能具有促认知作用。考虑到脑缺血与AD之间的密切关系,它们还可能减少脑缺血后的神经变性。一种研究性化合物CN-105(一种载脂蛋白E激动剂)在AD临床前研究中表现出非常好的效果,其针对术后痴呆的临床试验即将开始。