Department of Neurobiology and Behavior, University of California, Irvine, 3400A Biological Sciences III, Irvine, CA 92697-4545, USA.
Am J Pathol. 2010 Feb;176(2):870-80. doi: 10.2353/ajpath.2010.090452. Epub 2009 Dec 30.
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.
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。