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胆固醇转移抑制剂 U18666A 在神经退行性疾病中胆固醇机制研究中的潜在应用作为一种有效的研究工具。

Potential Use of the Cholesterol Transfer Inhibitor U18666A as a Potent Research Tool for the Study of Cholesterol Mechanisms in Neurodegenerative Disorders.

机构信息

Viro & Biotech, Tehran, Iran.

Department of Nanobiotechnology, Tehran, Iran.

出版信息

Mol Neurobiol. 2024 Jun;61(6):3503-3527. doi: 10.1007/s12035-023-03798-7. Epub 2023 Nov 23.

Abstract

Cholesterol is an essential component of mammalian cell membranes and a precursor for crucial signaling molecules. The brain contains the highest level of cholesterol in the body, and abnormal cholesterol metabolism links to many neurodegenerative disorders. The results indicate that faulty cholesterol metabolism is a common feature among people living with neurodegenerative conditions. The researchers suggest that restoring cholesterol levels may become a beneficial new strategy in treating certain neurodegenerative conditions. Several neurodegenerative disorders, such as Alzheimer's disease (AD), Niemann-Pick type C (NPC) disease, and Parkinson's disease (PD), have been connected to abnormalities in brain cholesterol metabolism. Consequently, using a lipid research tool is vital to study further and understand the effect of lipids in neurodegenerative disorders such as NPC, AD, PD, and Huntington's disease (HD). U18666A, also known as 3-(2-(diethylamino) ethoxy) androst-5-en-17-one, is a pharmaceutical drug that suppresses cholesterol trafficking and is a well-known class-2 amphiphile. U18666A has performed many functions, allowing for essential discoveries in lipid studies and shedding light on the pathophysiology of neurodegenerative disorders. Additionally, U18666A prevented the downregulation of low-density lipoprotein (LDL) receptors that are induced by LDL and led to the buildup of cholesterol in lysosomes. Numerous studies show that U18666A impacts the function of cholesterol trafficking to control the metabolism and transport of amyloid precursor proteins (APPs). Treating cortical neurons with U18666A may provide a new in vitro model system for studying the underlying molecular process of NPC, AD, HD, and PD. In this article, we review the mechanism and function of U18666A as a vital tool for studying cholesterol mechanisms in neurological diseases related to abnormal cholesterol metabolism, such as AD, NPC, HD, and PD.

摘要

胆固醇是哺乳动物细胞膜的重要组成部分,也是关键信号分子的前体。大脑中含有体内最高水平的胆固醇,异常的胆固醇代谢与许多神经退行性疾病有关。结果表明,胆固醇代谢异常是许多患有神经退行性疾病的人的共同特征。研究人员提出,恢复胆固醇水平可能成为治疗某些神经退行性疾病的有益新策略。几种神经退行性疾病,如阿尔茨海默病(AD)、尼曼-匹克 C 型(NPC)病和帕金森病(PD),都与大脑胆固醇代谢异常有关。因此,使用脂质研究工具对于进一步研究和了解 NPC、AD、PD 和亨廷顿病(HD)等神经退行性疾病中的脂质作用至关重要。U18666A,也称为 3-(2-(二乙氨基)乙氧基)雄甾-5-烯-17-酮,是一种抑制胆固醇转运的药物,是一种众所周知的 2 类两亲性化合物。U18666A 具有多种功能,为脂质研究中的重要发现提供了可能,并揭示了神经退行性疾病的病理生理学。此外,U18666A 阻止了 LDL 诱导的 LDL 受体下调,导致溶酶体中胆固醇的积累。许多研究表明,U18666A 影响胆固醇转运的功能,以控制淀粉样前体蛋白(APPs)的代谢和转运。用 U18666A 处理皮质神经元可能为研究 NPC、AD、HD 和 PD 等与异常胆固醇代谢相关的神经退行性疾病的潜在分子过程提供新的体外模型系统。在本文中,我们综述了 U18666A 作为研究与异常胆固醇代谢相关的神经退行性疾病(如 AD、NPC、HD 和 PD)中胆固醇机制的重要工具的作用机制和功能。

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