Reyna Nicole C, Clark Benjamin J, Hamilton Derek A, Pentkowski Nathan S
Department of Psychology, University of New Mexico, Albuquerque, NM, United States.
Front Aging Neurosci. 2023 Nov 10;15:1251075. doi: 10.3389/fnagi.2023.1251075. eCollection 2023.
Dementia remains one of the leading causes of morbidity and mortality in older adults. Alzheimer's disease (AD) is the most common type of dementia, affecting over 55 million people worldwide. AD is characterized by distinct neurobiological changes, including amyloid-beta protein deposits and tau neurofibrillary tangles, which cause cognitive decline and subsequent behavioral changes, such as distress, insomnia, depression, and anxiety. Recent literature suggests a strong connection between stress systems and AD progression. This presents a promising direction for future AD research. In this review, two systems involved in regulating stress and AD pathogenesis will be highlighted: serotonin (5-HT) and corticotropin releasing factor (CRF). Throughout the review, we summarize critical findings in the field while discussing common limitations with two animal models (3xTg-AD and TgF344-AD), novel pharmacotherapies, and potential early-intervention treatment options. We conclude by highlighting promising future pharmacotherapies and translational animal models of AD and anxiety.
痴呆症仍然是老年人发病和死亡的主要原因之一。阿尔茨海默病(AD)是最常见的痴呆类型,全球有超过5500万人受其影响。AD的特征是明显的神经生物学变化,包括β-淀粉样蛋白沉积和tau神经原纤维缠结,这些变化会导致认知能力下降以及随后的行为改变,如痛苦、失眠、抑郁和焦虑。最近的文献表明,应激系统与AD进展之间存在密切联系。这为未来的AD研究提供了一个有前景的方向。在这篇综述中,将重点介绍参与调节应激和AD发病机制的两个系统:血清素(5-HT)和促肾上腺皮质激素释放因子(CRF)。在整个综述过程中,我们总结了该领域的关键发现,同时讨论了两种动物模型(3xTg-AD和TgF344-AD)的常见局限性、新型药物疗法以及潜在的早期干预治疗方案。我们通过强调未来有前景的药物疗法以及AD和焦虑症的转化动物模型来结束本文。