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多奈哌齐对阿尔茨海默病患者胆固醇和氧化固醇血浆水平的影响。

Donepezil effects on cholesterol and oxysterol plasma levels of Alzheimer's disease patients.

机构信息

Laboratory of Neuroscience (LIM-27), Department and Institute of Psychiatry, University of Sao Paulo, Rua Dr. Ovídio Pires de Campos, 785, 3º andar, São Paulo, SP, 05403-010, Brazil.

Lipids Laboratory (LIM10), Faculty of Medical Sciences of the University of Sao Paulo, São Paulo, Brazil.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2018 Aug;268(5):501-507. doi: 10.1007/s00406-017-0838-2. Epub 2017 Aug 31.

Abstract

Cholesterol is an essential component in the structure and function of cell membranes and has been associated with the major pathological signatures of Alzheimer's disease (AD). To maintain brain cholesterol homeostasis, it is converted into 24(S)-hydroxycholesterol (24OHC) which can be driven through the blood-brain barrier. Several studies have already described a decrease in 24OHC and an increase of 27(S)-hydroxycholesterol (27OHC) in AD, as a reflection of disease burden, the loss of metabolically active neurons and the degree of structural atrophy. It is also well known that peripheral cholesterol is altered in AD patients. However, there are no data regarding effects of AD treatment in this cholesterol pathway. Since a study from our group indicated a significant increase in membrane phospholipid metabolism by donepezil, the aim of this study was to evaluate the effect of short- and long-term donepezil treatment on cholesterol and metabolites 24OHC and 27OHC in plasma of AD patients and in healthy volunteers. At baseline, we found a decrease of 24OHC (p = 0.003) in AD patients. Cholesterol levels increased with donepezil treatment (p = 0.04) but no differences were observed regarding 24OHC and 27OHC. However, these results confirm and extend previous studies demonstrating disturbed cholesterol turnover in Alzheimer's disease.

摘要

胆固醇是细胞膜结构和功能的重要组成部分,与阿尔茨海默病(AD)的主要病理特征有关。为了维持大脑胆固醇的平衡,胆固醇会转化为 24(S)-羟基胆固醇(24OHC),可以通过血脑屏障驱动。已有几项研究描述了 AD 患者中 24OHC 的减少和 27(S)-羟基胆固醇(27OHC)的增加,这反映了疾病负担、代谢活跃神经元的丧失和结构萎缩的程度。众所周知,AD 患者外周胆固醇也发生改变。然而,关于 AD 治疗对该胆固醇途径的影响尚无数据。由于我们的一项研究表明多奈哌齐显著增加了膜磷酯代谢,因此本研究旨在评估短期和长期多奈哌齐治疗对 AD 患者和健康志愿者血浆中胆固醇及其代谢物 24OHC 和 27OHC 的影响。在基线时,我们发现 AD 患者的 24OHC 减少(p=0.003)。胆固醇水平随多奈哌齐治疗而升高(p=0.04),但 24OHC 和 27OHC 无差异。然而,这些结果证实并扩展了先前的研究,表明阿尔茨海默病中胆固醇周转率紊乱。

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