Xie Guanfeng, Jiang Gege, Huang Liqin, Sun Shangqi, Wan Yuwei, Li Fang, Wu Bingjie, Zhang Ying, Li Xiaoyi, Xiong Bingwan, Xiong Jing
Department of Neurology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Pharmaceuticals (Basel). 2025 May 25;18(6):790. doi: 10.3390/ph18060790.
Lipid metabolism disorders represent a significant risk factor for the pathogenesis of Alzheimer's disease (AD). Apolipoprotein E (APOE) has been regarded as a pivotal regulator of lipid homeostasis in the central nervous system (CNS), with polymorphic alleles identified as genetic risk factors for late-onset AD. Despite advances in APOE research and the development of numerous pharmaceutical approaches targeting distinct APOE isoforms, there remain limited treatment approaches for AD that focus on lipid metabolic homeostasis. Consequently, it is necessary to reevaluate the lipid metabolic process in the CNS. Apolipoprotein A1 (APOA-I), a major component of high-density lipoprotein (HDL), plays a crucial role in reverse cholesterol transport from tissues to the liver to maintain lipid homeostasis. Over the past few decades, numerous studies have suggested a connection between reduced APOA-I levels and a higher risk of AD. APOA-I is synthesized exclusively in the liver and intestines, and there is a lack of conclusive evidence supporting its functional significance within the central nervous system, in contrast to APOE, which is produced locally by glial cells and neurons within the CNS. Moreover, APOA-I's ability to penetrate the blood-brain barrier (BBB) is still poorly understood, which causes its significance in central lipid metabolism and AD pathophysiology to be mainly disregarded. Recent advancements in tracing methodologies have underscored the essential role of APOA-I in regulating lipid metabolism in the CNS. This review aims to elucidate the physiological functions and metabolic pathways of APOA-I, integrating its associations with AD-related pathologies, risk factors, and potential therapeutic targets. Through this discourse, we aim to provide novel insights into the intricate relationship between AD and APOA-I, paving the way for future research in this field.
脂质代谢紊乱是阿尔茨海默病(AD)发病机制的一个重要风险因素。载脂蛋白E(APOE)被视为中枢神经系统(CNS)脂质稳态的关键调节因子,其多态性等位基因被确定为晚发性AD的遗传风险因素。尽管APOE研究取得了进展,并且开发了许多针对不同APOE异构体的药物方法,但针对AD的以脂质代谢稳态为重点的治疗方法仍然有限。因此,有必要重新评估CNS中的脂质代谢过程。载脂蛋白A1(APOA-I)是高密度脂蛋白(HDL)的主要成分,在胆固醇从组织逆向转运至肝脏以维持脂质稳态方面发挥着关键作用。在过去几十年中,大量研究表明APOA-I水平降低与AD风险升高之间存在关联。APOA-I仅在肝脏和肠道中合成,与CNS内由神经胶质细胞和神经元局部产生的APOE不同,目前缺乏确凿证据支持其在中枢神经系统中的功能意义。此外,APOA-I穿透血脑屏障(BBB)的能力仍知之甚少,这导致其在中枢脂质代谢和AD病理生理学中的重要性主要被忽视。追踪方法的最新进展强调了APOA-I在调节CNS脂质代谢中的重要作用。本综述旨在阐明APOA-I的生理功能和代谢途径,整合其与AD相关病理、风险因素和潜在治疗靶点的关联。通过这一论述,我们旨在为AD与APOA-I之间的复杂关系提供新的见解,为该领域的未来研究铺平道路。