Riekkinen P J, Laulumaa V, Sirviö J, Soininen H, Helkala E L
Department of Neurology, University of Kuopio, Finland.
Med Biol. 1987;65(2-3):83-8.
The purpose of this review is to survey some of the recent advances made in the understanding of the basic mechanisms underlying cognitive functions and dysfunctions in Alzheimer's disease (AD). Cholinergic projections from the nucleus basalis of Meynert (nbM), which are involved in AD, have been related to certain memory functions. Information processing, attention or arousal may, however, be influenced by nbM neurons more than primary memory mechanisms. Perforant pathway and subiculum projections, which presumably use glutamate as a neurotransmitter, are involved in AD leading to the disconnection of the hippocampus from the neocortical areas. The hippocampus and entorhinal cortex seem to play an important role in learning and memory. The hippocampus can be regarded as a relay station for the processing of recent episodic memory, but information is bound to memory storage in the cortical association areas. An important finding has been the plasticity changes in the hippocampus seen after the destruction of entorhinal cortex. Antemortem markers of AD have been under extensive study. Alz-50 antigen may be one of the most promising findings in this area, but no definite biological marker of AD currently exists. A medication for treatment of AD is also under development.
本综述的目的是概述近期在理解阿尔茨海默病(AD)认知功能及功能障碍的基本机制方面取得的一些进展。参与AD的来自梅纳特基底核(nbM)的胆碱能投射与某些记忆功能有关。然而,信息处理、注意力或觉醒可能比初级记忆机制更容易受到nbM神经元的影响。穿通通路和下托投射可能以谷氨酸作为神经递质,参与AD导致海马与新皮质区域断开连接。海马体和内嗅皮质似乎在学习和记忆中起重要作用。海马体可被视为处理近期情景记忆的中继站,但信息与皮质联合区的记忆存储相关。一个重要发现是在内嗅皮质受损后海马体出现的可塑性变化。AD的生前标志物一直在进行广泛研究。Alz-50抗原可能是该领域最有前景的发现之一,但目前尚无明确的AD生物学标志物。一种治疗AD的药物也正在研发中。