Olejnik Piotr, Golenia Aleksandra
Department of Neurology, Medical University of Warsaw, 02-091 Warsaw, Poland.
Cells. 2024 Nov 27;13(23):1962. doi: 10.3390/cells13231962.
Cognitive impairment is a major healthcare challenge worldwide, with vascular cognitive impairment (VCI) being its second leading cause after Alzheimer's disease. VCI is a heterogeneous group of cognitive disorders resulting from various vascular pathologies. Therefore, it is particularly difficult to determine its underlying cause and exact molecular basis. Nevertheless, the current understanding of the pathophysiological processes underlying VCI has changed and evolved in the last decades. The aim of this narrative review is to summarize the current state of knowledge on VCI pathogenesis and to analyze the potential role of the gut microbiota in this process, considering the most recent scientific reports and in accordance with the current understanding of these processes. Chronic cerebral hypoperfusion, which results in impaired blood supply, i.e., oxygen and nutrient deficiency, is the main underlying mechanism of VCI. Furthermore, chronic cerebral hypoperfusion triggers a cascade of molecular changes, starting with an energy imbalance, leading to glutamate excitotoxicity, acidotoxicity, and oxidative stress. Also, all of the above provoke the activation of microglia and the release of pro-inflammatory cytokines that recruit systemic immune cells and lead to their infiltration into the central nervous system, resulting in neuroinflammation. Blood-brain barrier dysfunction may occur at various stages of chronic cerebral hypoperfusion, ultimately increasing its permeability and allowing potentially toxic substances to enter the brain parenchyma. Gut microbiota and their metabolites, which have been identified in numerous inflammatory conditions, may also influence the pathophysiological processes of VCI.
认知障碍是全球主要的医疗保健挑战,血管性认知障碍(VCI)是仅次于阿尔茨海默病的第二大病因。VCI是一组由各种血管病变导致的异质性认知障碍。因此,确定其潜在病因和确切分子基础特别困难。然而,在过去几十年里,目前对VCI潜在病理生理过程的理解已经发生了变化和演变。本叙述性综述的目的是总结VCI发病机制的当前知识状态,并根据最新的科学报告以及对这些过程的当前理解,分析肠道微生物群在此过程中的潜在作用。慢性脑灌注不足会导致血液供应受损,即氧气和营养物质缺乏,这是VCI的主要潜在机制。此外,慢性脑灌注不足会引发一系列分子变化,始于能量失衡,导致谷氨酸兴奋性毒性、酸毒性和氧化应激。而且,上述所有情况都会引发小胶质细胞的激活和促炎细胞因子的释放,这些细胞因子会募集全身免疫细胞并导致它们浸润到中枢神经系统,从而导致神经炎症。血脑屏障功能障碍可能发生在慢性脑灌注不足的各个阶段,最终增加其通透性,使潜在的有毒物质进入脑实质。肠道微生物群及其代谢产物在多种炎症性疾病中已被确认,它们也可能影响VCI的病理生理过程。