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发现天然黄酮异补骨脂查耳酮作为阿尔茨海默病载脂蛋白E4(ApoE4)结构校正剂。

Discovery of Isobavachin, a Natural Flavonoid, as an Apolipoprotein E4 (ApoE4) Structure Corrector for Alzheimer's Disease.

作者信息

Patil Sachin P, Kuehn Bella R, McCullough Christina, Bates Dean, Hazim Hadil, Diallo Mamadou, Francois Naomie

机构信息

NanoBio Laboratory, Widener University, Chester, PA 19013, USA.

Department of Chemical Engineering, Widener University, Chester, PA 19013, USA.

出版信息

Molecules. 2025 Feb 18;30(4):940. doi: 10.3390/molecules30040940.

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by extensive neurodegeneration and consequent severe memory loss. Apolipoprotein E4 (ApoE4) is the strongest genetic risk factor for AD, with its pathological effects linked to structural instability and altered interactions with lipids and other important disease proteins including amyloid beta (Aβ) and tau (). Therefore, correcting and stabilizing the ApoE4 structure has emerged as a promising therapeutic strategy for mitigating its detrimental effects. In this study, we investigated naturally occurring bioavailable flavonoids as ApoE4 stabilizers, focusing on their potential to modulate ApoE4 structure and function. A comprehensive investigation of a focused database using our integrated computational and experimental screening protocol led to the identification of Isobavachin as a potential corrector and stabilizer of ApoE4 structure. In addition, a few other bioavailable flavonoids with similar stabilizing properties were identified, albeit to a much lesser extent as compared to Isobavachin. The findings support the therapeutic potential of flavonoids as ApoE4 modulators and highlight Isobavachin as a lead candidate for further preclinical evaluation. These results provide new insights into the pharmacological targeting of ApoE4 and open avenues for the development of flavonoid-based, ApoE-directed therapies for AD.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,其特征是广泛的神经退行性变以及随之而来的严重记忆丧失。载脂蛋白E4(ApoE4)是AD最强的遗传风险因素,其病理作用与结构不稳定以及与脂质和其他重要疾病蛋白(包括β淀粉样蛋白(Aβ)和tau蛋白)相互作用的改变有关。因此,纠正和稳定ApoE4结构已成为减轻其有害影响的一种有前景的治疗策略。在本研究中,我们研究了天然存在的具有生物利用度的类黄酮作为ApoE4稳定剂,重点关注它们调节ApoE4结构和功能的潜力。使用我们的综合计算和实验筛选方案对一个重点数据库进行全面研究后,确定异补骨脂素是ApoE4结构的潜在校正剂和稳定剂。此外,还鉴定出了其他一些具有类似稳定特性的具有生物利用度的类黄酮,尽管与异补骨脂素相比程度要小得多。这些发现支持了类黄酮作为ApoE4调节剂的治疗潜力,并突出了异补骨脂素作为进一步临床前评估的主要候选物。这些结果为ApoE4的药理学靶向提供了新的见解,并为开发基于类黄酮的、针对ApoE的AD治疗方法开辟了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2089/11858207/1a03b7234c02/molecules-30-00940-g001.jpg

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