Department of Anatomy and Cell Biology, The University of Illinois at Chicago, Chicago, IL, United States.
Department of Pharmacology, The University of Illinois at Chicago, Chicago, IL, United States; Department of Anesthesiology, The University of Illinois at Chicago, Chicago, IL, United States.
Int Rev Neurobiol. 2020;155:235-269. doi: 10.1016/bs.irn.2020.03.020.
Some metabolic disorders, such as type 2 diabetes mellitus (T2DM) are risk factors for the development of cognitive deficits and Alzheimer's disease (AD). Epidemiological studies suggest that in people with T2DM, the risk of developing dementia is 2.5 times higher than that in the non-diabetic population. The signaling pathways that underlie the increased risk and facilitate cognitive deficits are not fully understood. In fact, the cause of memory deficits in AD is not fully elucidated. The dentate gyrus of the hippocampus plays an important role in memory formation. Hippocampal neurogenesis is the generation of new neurons and glia in the adult brain throughout life. New neurons incorporate in the granular cell layer of the dentate gyrus and play a role in learning and memory and hippocampal plasticity. A large body of studies suggests that hippocampal neurogenesis is impaired in mouse models of AD and T2DM. Recent evidence shows that hippocampal neurogenesis is also impaired in human patients exhibiting mild cognitive impairment or AD. This review discusses the role of hippocampal neurogenesis in the development of cognitive deficits and AD, and considers inflammatory and endothelial signaling pathways in T2DM that may compromise hippocampal neurogenesis and cognitive function, leading to AD.
一些代谢紊乱,如 2 型糖尿病(T2DM),是认知障碍和阿尔茨海默病(AD)发展的危险因素。流行病学研究表明,在 2 型糖尿病患者中,痴呆的风险比非糖尿病患者高 2.5 倍。导致风险增加和促进认知障碍的信号通路尚未完全阐明。事实上,AD 患者记忆缺陷的原因尚未完全阐明。海马的齿状回在记忆形成中起着重要作用。海马神经发生是指成年期大脑中不断产生新的神经元和神经胶质。新神经元整合到齿状回的颗粒细胞层中,在学习和记忆以及海马可塑性中发挥作用。大量研究表明,AD 和 T2DM 的小鼠模型中存在海马神经发生受损。最近的证据表明,在表现出轻度认知障碍或 AD 的人类患者中,海马神经发生也受损。这篇综述讨论了海马神经发生在认知障碍和 AD 发展中的作用,并考虑了 T2DM 中的炎症和内皮信号通路,这些信号通路可能损害海马神经发生和认知功能,导致 AD。