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美金刚可改善转基因小鼠的认知功能并减少类似阿尔茨海默病的神经病理学改变。

Memantine improves cognition and reduces Alzheimer's-like neuropathology in transgenic mice.

机构信息

Department of Neurobiology and Behavior, University of California, Irvine, 3400A Biological Sciences III, Irvine, CA 92697-4545, USA.

出版信息

Am J Pathol. 2010 Feb;176(2):870-80. doi: 10.2353/ajpath.2010.090452. Epub 2009 Dec 30.

Abstract

Memantine is an N-methyl-d-aspartate receptor antagonist that is approved for the treatment of moderate to severe Alzheimer's disease (AD). In this study, three groups of triple-transgenic (3xTg-AD) mice with differing levels of AD-like pathology (6, 9, and 15 months of age) were treated for 3 months with doses of memantine equivalent to those used in humans. After the treatment, memantine-treated mice had restored cognition and significantly reduced the levels of insoluble amyloid-beta (Abeta), Abeta dodecamers (Abeta*56), prefibrillar soluble oligomers, and fibrillar oligomers. The effects on pathology were stronger in older, more impaired animals. Memantine treatment also was associated with a decline in the levels of total tau and hyperphosphorylated tau. Finally, memantine pre-incubation prevented Abeta-induced inhibition of long-term potentiation in hippocampal slices of cognitively normal mice. These results suggest that the effects of memantine treatment on AD brain include disease modification and prevention of synaptic dysfunction.

摘要

美金刚是一种 N-甲基-D-天冬氨酸受体拮抗剂,已被批准用于治疗中重度阿尔茨海默病(AD)。在这项研究中,三组具有不同程度 AD 样病理学的三转基因(3xTg-AD)小鼠(6、9 和 15 月龄)接受了相当于人类使用剂量的美金刚治疗 3 个月。治疗后,美金刚治疗的小鼠认知能力得到恢复,可溶性淀粉样β(Abeta)、Abeta 十二聚体(Abeta*56)、前纤维状可溶性寡聚物和纤维状寡聚物的水平显著降低。在年龄更大、损伤更严重的动物中,这些作用更为明显。美金刚治疗还与总 tau 和过度磷酸化 tau 水平的下降有关。最后,美金刚孵育前处理可预防认知正常小鼠海马切片中 Abeta 诱导的长时程增强抑制。这些结果表明,美金刚治疗 AD 脑的作用包括疾病修饰和预防突触功能障碍。

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