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研究一种载有姜黄素的聚乳酸-羟基乙酸共聚物-聚乙二醇-聚乳酸-羟基乙酸共聚物热敏水凝胶用于预防阿尔茨海默病。

Investigating a Curcumin-Loaded PLGA-PEG-PLGA Thermo-Sensitive Hydrogel for the Prevention of Alzheimer's Disease.

作者信息

Lin Yi-Wen, Fang Chih-Hsiang, Yang Ching-Yun, Liang Ya-Jyun, Lin Feng-Huei

机构信息

Institute of Biomedical Engineering, National Taiwan University, No.1, Sec. 1, Jen-Ai Road, Taipei 10617, Taiwan.

Trauma and Emergency Center, China Medical University Hospital, No.2, Xueshi Rd., North Dist., Taichung 40454, Taiwan.

出版信息

Antioxidants (Basel). 2022 Apr 7;11(4):727. doi: 10.3390/antiox11040727.

Abstract

In Alzheimer's disease (AD), the most common cause of dementia, patients generally forget to take pills or skip medication due to side effects, affecting the treatment efficacy. In this study, we combined a poly(lactic-co-glycolic acid), (PLGA)-poly(ethylene glycol), and (PEG)-PLGA thermo-sensitive hydrogel with curcumin (PGC) to deliver an intramuscular injection that could continuously release curcumin and maintain it at a constant level in blood to prevent AD development or progression. We evaluated the drug release profile and cytotoxicity of PGC and its effects on AD pathology through in vitro and in vivo studies and on cognitive function through an aluminum-chloride-induced AD rat model. In the in vitro study, PGC exhibited a lack of cytotoxicity, excellent anti-inflammatory and antioxidant properties, and microglial modulation. In the Morris water maze test, the PGC injection-administered AD rats presented well-focused searching behavior with the shortest swimming path and longest retention times in the quadrant where the platform was initially located. Furthermore, PGC reduced amyloid-beta aggregation and deposition and significantly increased hippocampal activity. This study demonstrated that intramuscular PGC injection can effectively prevent AD development or progression in rats without inducing toxicity; therefore, this strategy could help overcome the present challenges in AD management in humans.

摘要

在最常见的痴呆病因阿尔茨海默病(AD)中,患者通常会因副作用而忘记服药或漏服,从而影响治疗效果。在本研究中,我们将聚乳酸 - 乙醇酸共聚物(PLGA)-聚乙二醇(PEG)-PLGA热敏水凝胶与姜黄素(PGC)结合,制成可进行肌肉注射的制剂,使其能够持续释放姜黄素并在血液中维持恒定水平,以预防AD的发生或进展。我们通过体外和体内研究评估了PGC的药物释放曲线、细胞毒性及其对AD病理的影响,并通过氯化铝诱导的AD大鼠模型评估了其对认知功能的影响。在体外研究中,PGC表现出无细胞毒性、优异的抗炎和抗氧化特性以及对小胶质细胞的调节作用。在莫里斯水迷宫试验中,注射PGC的AD大鼠表现出良好的聚焦搜索行为,在平台最初所在象限的游泳路径最短,停留时间最长。此外,PGC减少了β-淀粉样蛋白的聚集和沉积,并显著增强了海马体的活性。本研究表明,肌肉注射PGC可有效预防大鼠AD的发生或进展,且不会产生毒性;因此,该策略有助于克服目前人类AD治疗中的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54fd/9026862/7ae10e8b2370/antioxidants-11-00727-g001.jpg

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