作为潜在抗老年痴呆药物的酰胺羧酸盐的药理评估:抗自由基、酶抑制、动物模型模拟和行为研究。

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mater H Mahnashi, Saqib Ali, Osama M Alshehri, Ibrahim Abdullah Almazni, Saeed Ahmed Asiri, Abdul Sadiq, Rehman Zafar, Muhammad Saeed Jan
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种神经系统疾病,会逐渐发展但不可逆转地导致痴呆,并且难以预防和治疗。这种疾病的发展有相当长的时间可以干预。需要科学进步来帮助研究人员确定预防和治疗疾病的有效方法。本研究旨在探究治疗注意力缺失症的潜在介质,合成了五种新的羧酸酰胺锌复合物(AAZ9-AAZ13),并通过光谱和理化技术对其进行了表征。根据胆碱酯酶抑制机制进行了生物学评价。该制备方法有效地合成了目标分子。体外药理活性评估涉及 AChE/BChE 抑制作用和抗氧化潜力。所有合成化合物对这两种酶的活性都高于或相当于标准药物金刚烷胺(一种可逆性抑制剂),但化合物 AAZ10 显示的 IC50 值为 0.0013 µM(AChE)和 0.061 µM(BChE),是 AChE/BChE 双重抑制的高值,并具有强大的抗氧化效果。结构活性关系(SAR)表明,化合物 AAZ10 的强效活性是由于在芳香环的正交位置存在硝基簇。研究人员还对合成的强效化合物 AAZ10 进行了体内抗老年痴呆活性和抗氧化活性的研究。通过分子对接研究揭示了所有合成化合物与酶结合口袋的结合方式,分析了与氨基酸(AA)残基的最佳姿势相互作用,从而对酶抑制机制有了更深入的了解。结果表明,合成的酰胺羧酸锌(II)可作为治疗阿尔茨海默氏症的有效药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological evaluations of amide carboxylates as potential anti-Alzheimer agents: anti-radicals, enzyme inhibition, simulation and behavioral studies in animal models.

Alzheimer's disease (AD) is a neurological disorder that progresses gradually but irreversibly leading to dementia and is difficult to prevent and treat. There is a considerable time window in which the progression of the disease can be intervened. Scientific advances were required to help the researchers to identify the effective methods for the prevention and treatment of disease. This research was designed to investigate potential mediators for the remedy of AD, five new carboxylate amide zinc complexes (AAZ9-AAZ13) were synthesized and characterized by spectroscopic and physicochemical techniques. The biological evaluation was carried out based on the cholinesterase inhibitory mechanism. The preparation methodology provided the effective synthesis of targeted moieties. The in vitro pharmacological activities were evaluated involving AChE/BChE inhibition and antioxidant potential. All synthesized compounds displayed activity against both enzymes in higher or comparable to the standard drug Galantamine, a reversible inhibitor but the results displayed by compound AAZ10 indicated IC50 of 0.0013 µM (AChE) and 0.061 µM (BChE) as high values for dual AChE/BChE inhibition with potent anti-oxidant results. Structure activity relationship (SAR) indicated that the potent activity of compound AAZ10 appeared due to the presence of nitro clusters at the ortho position of an aromatic ring. The potent synthesized compound AAZ10 was also explored for the in-vivo Anti-Alzheimer activity and anti-oxidant activity. Binding approaches of all synthesized compounds were revealed through molecular docking studies concerning binding pockets of enzymes that analyzed the best posture interaction with amino acid (AA) residues providing an appreciable understanding of enzyme inhibitory mechanisms. Results indicate that synthesized zinc (II) amide carboxylates can behave as an effective remedy in the treatment of Alzheimer's disease.Communicated by Ramaswamy H. Sarma.

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来源期刊
Journal of Biomolecular Structure & Dynamics
Journal of Biomolecular Structure & Dynamics 生物-生化与分子生物学
CiteScore
8.90
自引率
9.10%
发文量
597
审稿时长
2 months
期刊介绍: The Journal of Biomolecular Structure and Dynamics welcomes manuscripts on biological structure, dynamics, interactions and expression. The Journal is one of the leading publications in high end computational science, atomic structural biology, bioinformatics, virtual drug design, genomics and biological networks.
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