Hunan Provincial Key Laboratory of Physical Fitness and Sports Rehabilitation, Hunan Normal University, Changsha, 410012, China.
Key Laboratory of Protein Chemistry and Developmental Biology of Ministry of Education, Hunan Normal University, Changsha, 410081, China.
Mol Neurobiol. 2023 Dec;60(12):6852-6868. doi: 10.1007/s12035-023-03529-y. Epub 2023 Jul 28.
Alzheimer's disease (AD) is a degenerative disease of the central nervous system. Numerous studies have shown that imbalances in cholesterol homeostasis in the brains of AD patients precede the onset of clinical symptoms. In addition, cholesterol deposition has been observed in the brains of AD patients even though peripheral cholesterol does not enter the brain through the blood‒brain barrier (BBB). Studies have demonstrated that cholesterol metabolism in the brain is associated with many pathological conditions, such as amyloid beta (Aβ) production, Tau protein phosphorylation, oxidative stress, and inflammation. In 2022, some scholars put forward a new hypothesis of AD: the disease involves lipid invasion and its exacerbation of the abnormal metabolism of cholesterol in the brain. In this review, by discussing the latest research progress, the causes and effects of cholesterol retention in the brains of AD patients are analyzed and discussed. Additionally, the possible mechanism through which AD may be improved by targeting cholesterol is described. Finally, we propose that improving the impairments in cholesterol removal observed in the brains of AD patients, instead of further reducing the already impaired cholesterol synthesis in the brain, may be the key to preventing cholesterol deposition and improving the corresponding pathological symptoms.
阿尔茨海默病(AD)是一种中枢神经系统退行性疾病。大量研究表明,AD 患者大脑中的胆固醇稳态失衡先于临床症状出现。此外,尽管外周胆固醇不能通过血脑屏障(BBB)进入大脑,但在 AD 患者的大脑中仍观察到胆固醇沉积。研究表明,大脑中的胆固醇代谢与许多病理状况有关,如淀粉样β(Aβ)产生、Tau 蛋白磷酸化、氧化应激和炎症。2022 年,一些学者提出了 AD 的一个新假设:该疾病涉及脂质入侵及其加剧大脑中胆固醇的异常代谢。在这篇综述中,通过讨论最新的研究进展,分析和讨论了 AD 患者大脑中胆固醇滞留的原因和影响。此外,还描述了通过靶向胆固醇可能改善 AD 的可能机制。最后,我们提出,改善 AD 患者大脑中观察到的胆固醇清除受损,而不是进一步降低已经受损的大脑胆固醇合成,可能是防止胆固醇沉积和改善相应病理症状的关键。