Hassan E Mohammed, James C Nelson, S Alex Marshall
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引用次数: 0
摘要
阿尔茨海默病(AD)是最常见的痴呆症形式,具有特征性的生物标志物。临床上,阿尔茨海默病表现为记忆、推理和决策能力下降,但记忆丧失与海马损伤特别相关。同样,过量的乙醇摄入也会破坏海马的功能和完整性。为了评估AD病理和乙醇的潜在共同后果,5xFAD小鼠每天给予5 g/kg乙醇,持续10天。免疫组织化学分析显示,乙醇和AD融合导致小胶质细胞和星形胶质细胞衰老,并增加海马a ß-斑块形成。尽管这些潜在的神经退行性变机制加剧,但乙醇暴露和ad相关基因型对氟jade C (FJC)+细胞或新物体识别任务中的认知缺陷没有加性影响。总的来说,这些结果首次描述了乙醇暴露对5xFAD小鼠模型成年早期的影响。总之,这些发现支持了酒精可以影响阿尔茨海默病病理的观点;然而,参与AD进展的机制(例如,神经胶质活化和a ß-斑块)可能在病理证据(例如,认知能力下降或神经元丧失)之前受到影响。
Ethanol Exacerbates the Alzheimer's Disease Pathology in the 5xFAD Mouse Model.
Alzheimer's disease (AD) is the most common form of dementia with characteristic biological markers. Clinically, AD presents as declines in memory, reasoning, and decision making, but the loss of memory is particularly associated with hippocampal damage. Likewise, excessive ethanol consumption has been found to disrupt hippocampal function and integrity. To assess the potential shared consequences of AD pathology and ethanol, 5xFAD mice were administered 5 g/kg ethanol daily for 10 days. Immunohistochemical analysis revealed ethanol and AD converged to lead to microglial and astrocytic senescence as well as increased Aß-plaque formation in the hippocampus. Despite the exacerbation of these potential mechanisms of neurodegeneration, there were no additive effects of ethanol exposure and AD-related genotype on Fluoro-Jade C (FJC)+ cells or cognitive deficits in the novel object recognition task. Overall, these results are the first to characterize the effects of ethanol exposure on early adulthood in the 5xFAD mouse model. Together these findings support the idea that alcohol can influence AD pathology; however, the mechanisms involved in AD progression (e.g., glial activation and Aß-plaque) may be impacted prior to evidence of pathology (e.g., cognitive decline or neuronal loss).