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阿尔茨海默病中海马的振荡活动:寻找早期生物标志物?

Hippocampal oscillatory activity in Alzheimer's disease: toward the identification of early biomarkers?

机构信息

Laboratoire de Neurosciences Comportementales et Adaptatives (LNCA),Centre National de la Recherche Scientifique (CNRS), F-67000 Strasbourg, France. ; Université de Strasbourg, Faculté de Psychologie, F-67000 Strasbourg, France.

出版信息

Aging Dis. 2013 Jan 23;4(3):134-40. Print 2013 Jun.

PMID:23730529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3660123/
Abstract

Alzheimer's disease (AD) develops for a yet unknown period of time and can progress undiagnosed for years before its first clinical manifestation consisting of characteristic cognitive impairments. Current AD treatments offer only a small symptomatic benefit, likely because AD is diagnosed when the pathology is already well advanced, whereas treatments may be most efficient in the early phases of pathology. An accurate, early marker of AD is therefore needed to help diagnose AD earlier. It is now well documented that AD patients and animal models of AD exhibit reorganization of hippocampal and cortical networks. This reorganization is initiated by an early imbalance between excitation and inhibition, leading to altered network activity. The mechanisms underlying these changes are unknown but recent evidence suggests that either soluble amyloid-beta (Aß) or fibrillar forms of Aß are central to various network alterations observed in AD. However, recent evidence also suggests that Aβ over-production in animal models is not systematically linked to network over-excitation. We hypothesize here that early changes in the excitation-inhibition balance within the hippocampus occurs much earlier than currently believed and initially produces only slight changes in overall hippocampal activity. In this review, we introduce the concept according to which the subtle changes in theta and gamma rhythms might occur during the very first stages of AD and thus could be used as a possible predictor for the disease.

摘要

阿尔茨海默病(AD)的发展时间尚不清楚,在其首次出现以特征性认知障碍为表现的临床症状之前,可能会未经诊断而持续多年进展。目前的 AD 治疗方法仅提供了很小的对症益处,这可能是因为 AD 在病理已经相当严重时才被诊断出来,而治疗可能在病理的早期阶段最为有效。因此,需要一种准确的、早期的 AD 标志物来帮助更早地诊断 AD。现在已经有充分的证据表明,AD 患者和 AD 的动物模型表现出海马和皮质网络的重组。这种重组是由兴奋和抑制之间的早期失衡引发的,导致网络活动改变。这些变化的机制尚不清楚,但最近的证据表明,可溶性淀粉样蛋白-β(Aβ)或 Aβ 的纤维形式是 AD 中观察到的各种网络改变的核心。然而,最近的证据还表明,动物模型中的 Aβ 过度产生与网络过度兴奋并不系统相关。我们在这里假设,海马内兴奋-抑制平衡的早期变化发生得比目前认为的要早得多,并且最初只会导致整体海马活动的轻微变化。在这篇综述中,我们介绍了这样一个概念,即在 AD 的最初阶段,θ 和γ 节律的细微变化可能就已经发生,因此可以作为疾病的一个可能预测指标。

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