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Current treatment for Alzheimer disease and future prospects.阿尔茨海默病的当前治疗方法及未来前景。
Alzheimer Dis Assoc Disord. 2003 Jul-Sep;17 Suppl 4:S105-13. doi: 10.1097/00002093-200307004-00005.
2
Cholinergic function and Alzheimer's disease.胆碱能功能与阿尔茨海默病。
Int J Geriatr Psychiatry. 2003 Sep;18(Suppl 1):S1-5. doi: 10.1002/gps.935.
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The protective effect of ganstigmine against amyloid beta 25-35 neurotoxicity on chicken cortical neurons is independent from the cholinesterase inhibition.
Neurosci Lett. 2003 May 8;341(3):181-4. doi: 10.1016/s0304-3940(03)00125-3.
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Beta-amyloid plaques in a model for sporadic Alzheimer's disease based on transgenic anti-nerve growth factor antibodies.基于转基因抗神经生长因子抗体的散发性阿尔茨海默病模型中的β-淀粉样蛋白斑块
Mol Cell Neurosci. 2002 Sep;21(1):15-28. doi: 10.1006/mcne.2002.1163.
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Nerve growth factor and galantamine ameliorate early signs of neurodegeneration in anti-nerve growth factor mice.神经生长因子和加兰他敏可改善抗神经生长因子小鼠的早期神经退行性变迹象。
Proc Natl Acad Sci U S A. 2002 Sep 17;99(19):12432-7. doi: 10.1073/pnas.192442999. Epub 2002 Aug 30.
6
Acute cholinergic rescue of synaptic plasticity in the neurodegenerating cortex of anti-nerve-growth-factor mice.急性胆碱能挽救抗神经生长因子小鼠神经退行性变皮质中的突触可塑性。
Eur J Neurosci. 2002 Mar;15(6):1030-6. doi: 10.1046/j.1460-9568.2002.01937.x.
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Alzheimer's disease: genes, proteins, and therapy.阿尔茨海默病:基因、蛋白质与治疗
Physiol Rev. 2001 Apr;81(2):741-66. doi: 10.1152/physrev.2001.81.2.741.
8
Amino-terminal modification and tyrosine phosphorylation of [corrected] carboxy-terminal fragments of the amyloid precursor protein in Alzheimer's disease and Down's syndrome brain.阿尔茨海默病和唐氏综合征大脑中淀粉样前体蛋白羧基末端片段的氨基末端修饰和酪氨酸磷酸化[校正后]
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9
Cholinesterase inhibitors stabilize Alzheimer disease.胆碱酯酶抑制剂可稳定阿尔茨海默病病情。
Neurochem Res. 2000 Oct;25(9-10):1185-90. doi: 10.1023/a:1007679709322.
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Biochemical and neurobehavioral profile of CHF2819, a novel, orally active acetylcholinesterase inhibitor for Alzheimer's disease.
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加兰他敏和多奈哌齐可改善AD11抗神经生长因子转基因小鼠的神经退行性变。

Ganstigmine and donepezil improve neurodegeneration in AD11 antinerve growth factor transgenic mice.

作者信息

Capsoni Simona, Giannotta Sabina, Stebel Marco, Garcia Addys Ancheta, De Rosa Roberta, Villetti Gino, Imbimbo Bruno Pietro, Pietra Claudio, Cattaneo Antonino

机构信息

Lay Line Genomics S.p.A., Rome, Italy.

出版信息

Am J Alzheimers Dis Other Demen. 2004 May-Jun;19(3):153-60. doi: 10.1177/153331750401900303.

DOI:10.1177/153331750401900303
PMID:15214201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10833932/
Abstract

Ganstigmine (CHF2819) is an acetylcholinesterase inhibitor that increases acetylcholine in rat hippocampus and ameliorates scopolamine-induced amnesia. In this article, we examined whether and how ganstigmine might prevent or rescue the neurodegenerative phenotype in AD11 antinerve growth factor (anti-NGF) mice, a transgenic model for Alzheimer's disease. The effects of ganstigmine were compared with those obtained after administration of donepezil. Results demonstrate that intraperitoneal and oral administration of ganstigmine and donepezil can reverse the cholinergic and behavioral deficit in AD11 mice but not the amyloid and phosphotau accumulation, uncovering different mechanisms leading to neurodegeneration in AD11 mice.

摘要

加兰他敏(CHF2819)是一种乙酰胆碱酯酶抑制剂,可增加大鼠海马体中的乙酰胆碱,并改善东莨菪碱诱导的失忆。在本文中,我们研究了加兰他敏是否以及如何预防或挽救AD11抗神经生长因子(anti-NGF)小鼠(一种阿尔茨海默病转基因模型)的神经退行性表型。将加兰他敏的作用与服用多奈哌齐后的作用进行了比较。结果表明,腹腔注射和口服加兰他敏及多奈哌齐可逆转AD11小鼠的胆碱能和行为缺陷,但不能逆转淀粉样蛋白和磷酸化tau蛋白的积累,揭示了AD11小鼠神经退行性变的不同机制。