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重新审视阿尔茨海默病发病机制中的胆碱能假说。

Revisiting the cholinergic hypothesis in the development of Alzheimer's disease.

机构信息

Canadian Centre for Behavioural Neuroscience, Department of Neuroscience, University of Lethbridge; 4401 University Drive, Lethbridge, AB, Canada.

出版信息

Neurosci Biobehav Rev. 2011 May;35(6):1397-409. doi: 10.1016/j.neubiorev.2011.03.001. Epub 2011 Mar 12.

Abstract

Alzheimer's disease (AD) is the most common form of dementia affecting the elderly population today; however, there is currently no accurate description of the etiology of this devastating disorder. No single factor has been demonstrated as being causative; however, an alternative co-factors theory suggests that the interaction of multiple risk factors is responsible for AD. We have used this model, in combination with the original cholinergic hypothesis of AD to propose a "new" cholinergic hypothesis that we present in this review. This new version takes into account recent findings from the literature and our reports of removal of medial septum cholinergic projections to the hippocampus reduces both behavioural and anatomical plasticity, resulting in greater cognitive impairment in response to secondary insults (stress, injury, disease, etc.). We will first summarize the experimental results and discuss some potential mechanisms that could explain our results. We will then present our 'new' version of the cholinergic hypothesis and how it relates to the field of AD research today. Finally we will discuss some of the implications for treatment that arise from this model and present directions for future study.

摘要

阿尔茨海默病(AD)是当今影响老年人群体的最常见的痴呆形式;然而,目前对于这种破坏性疾病的病因还没有准确的描述。没有单一的因素被证明是致病的;然而,一种替代的共同因素理论表明,多种危险因素的相互作用是导致 AD 的原因。我们使用了这种模型,结合 AD 的原始胆碱能假说,提出了一个“新”的胆碱能假说,我们在这篇综述中提出。这个新版本考虑了来自文献的最新发现和我们的报告,即去除内侧隔胆碱能投射到海马体减少了行为和解剖可塑性,导致对二次损伤(压力、损伤、疾病等)的认知损伤更大。我们将首先总结实验结果,并讨论一些可能解释我们结果的潜在机制。然后,我们将提出我们的“新”胆碱能假说版本,以及它与当今 AD 研究领域的关系。最后,我们将讨论从该模型中产生的一些治疗意义,并为未来的研究提供方向。

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