Florent-Béchard Sabrina, Desbène Cédric, Garcia Pierre, Allouche Ahmad, Youssef Ihsen, Escanyé Marie-Christine, Koziel Violette, Hanse Marine, Malaplate-Armand Catherine, Stenger Christophe, Kriem Badreddine, Yen-Potin Frances T, Olivier Jean Luc, Pillot Thierry, Oster Thierry
Lipidomix, ENSAIA - INPL, Nancy-Université, France.
Biochimie. 2009 Jun;91(6):804-9. doi: 10.1016/j.biochi.2009.03.004. Epub 2009 Mar 18.
In the absence of efficient diagnostic and therapeutic tools, Alzheimer's disease (AD) is a major public health concern due to longer life expectancy in the Western countries. Although the precise cause of AD is still unknown, soluble beta-amyloid (Abeta) oligomers are considered the proximate effectors of the synaptic injury and neuronal death occurring in the early stages of AD. Abeta oligomers may directly interact with the synaptic membrane, leading to impairment of synaptic functions and subsequent signalling pathways triggering neurodegeneration. Therefore, membrane structure and lipid status should be considered determinant factors in Abeta-oligomer-induced synaptic and cell injuries, and therefore AD progression. Numerous epidemiological studies have highlighted close relationships between AD incidence and dietary patterns. Among the nutritional factors involved, lipids significantly influence AD pathogenesis. It is likely that maintenance of adequate membrane lipid content could prevent the production of Abeta peptide as well as its deleterious effects upon its interaction with synaptic membrane, thereby protecting neurons from Abeta-induced neurodegeneration. As major constituents of neuronal lipids, n-3 polyunsaturated fatty acids are of particular interest in the prevention of AD valuable diet ingredients whose neuroprotective properties could be essential for designing preventive nutrition-based strategies. In this review, we discuss the functional relevance of neuronal membrane features with respect to susceptibility to Abeta oligomers and AD pathogenesis, as well as the prospective capacities of lipids to prevent or to delay the disease.
在缺乏有效诊断和治疗工具的情况下,由于西方国家预期寿命延长,阿尔茨海默病(AD)成为一个主要的公共卫生问题。尽管AD的确切病因仍不清楚,但可溶性β-淀粉样蛋白(Aβ)寡聚体被认为是AD早期发生的突触损伤和神经元死亡的直接效应物。Aβ寡聚体可能直接与突触膜相互作用,导致突触功能受损以及随后触发神经退行性变的信号通路异常。因此,膜结构和脂质状态应被视为Aβ寡聚体诱导的突触和细胞损伤以及AD进展的决定性因素。众多流行病学研究强调了AD发病率与饮食模式之间的密切关系。在涉及的营养因素中,脂质对AD发病机制有显著影响。维持适当的膜脂质含量可能会阻止Aβ肽的产生及其与突触膜相互作用时的有害影响,从而保护神经元免受Aβ诱导的神经退行性变。作为神经元脂质的主要成分,n-3多不饱和脂肪酸在预防AD方面特别受关注,其神经保护特性对于设计基于预防性营养的策略可能至关重要。在这篇综述中,我们讨论了神经元膜特征与对Aβ寡聚体的易感性和AD发病机制的功能相关性,以及脂质预防或延缓该疾病的潜在能力。