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迷迭香中分离得到的 Nepitrin 通过分子对接和抗东莨菪碱诱导的记忆障碍对小鼠的作用。

Molecular docking and antiamnesic effects of nepitrin isolated from Rosmarinus officinalis on scopolamine-induced memory impairment in mice.

机构信息

Department of Pharmacy, University of Malakand, Chakdara, Dir (Lower), KPK, Pakistan.

Department of Pharmacy, University of Swabi, KPK, Pakistan.

出版信息

Biomed Pharmacother. 2017 Dec;96:700-709. doi: 10.1016/j.biopha.2017.09.121. Epub 2017 Nov 6.

DOI:10.1016/j.biopha.2017.09.121
PMID:29040957
Abstract

Rosmarinus officinalis has long been known as the herb of remembrance. The present study was undertaken to investigate the anti-amnesic effects of nepitrin isolated from Rosmarinus officinalis using in-vivo models of Y-maze and novel object recognition test (NORT) along with in vitro antioxidant and acetylcholinesterase (AChE) and buterylcholinesterase (BuChE) inhibition potential. Nepitrin showed a concentration dependent inhibition of AChE and BuChE enzymes with IC values of 65 and 72μg/mL, respectively and antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2, 2'-azinobis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS) with IC values 270 and 210μg/mL, respectively. In mice, nepitrin reversed the amnesia induced by scopolamine as indicated by a dose-dependent increase in spontaneous alternation performance in the Y-maze task (p <0.05 versus scopolamine) and increase in the discrimination index in the novel object recognition test (NORT) comparable to the standard drug donepezil 2mg/kg. Molecular docking studies were performed and the GlideScore of nepitrin was consistent with its experimental AChE inhibitory activities. Nepitrin occupied the same binding site forming similar interactions to those formed by donepezil in the crystal structure. Thus, nepitrin could provide a lead for the development of therapeutic agent useful in cognition and memory disorders such as Alzheimer's disease.

摘要

迷迭香自古以来就被称为记忆之草。本研究旨在通过 Y 型迷宫和新物体识别测试(NORT)体内模型以及体外抗氧化和乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BuChE)抑制潜力,来研究从迷迭香中分离得到的尼泊亭的抗健忘作用。尼泊亭对 AChE 和 BuChE 酶表现出浓度依赖性抑制作用,IC 值分别为 65 和 72μg/mL,并且对 2,2-二苯基-1-苦基肼基(DPPH)和 2,2'-联氮双-3-乙基苯并噻唑啉-6-磺酸(ABTS)具有抗氧化活性,IC 值分别为 270 和 210μg/mL。在小鼠中,尼泊亭可逆转东莨菪碱引起的健忘症,表现在 Y 型迷宫任务中自发交替性能呈剂量依赖性增加(与东莨菪碱相比,p <0.05),并且新物体识别测试(NORT)中的辨别指数增加,与标准药物多奈哌齐 2mg/kg 相当。进行了分子对接研究,尼泊亭的 GlideScore 与其实验性 AChE 抑制活性一致。尼泊亭占据相同的结合位点,与晶体结构中多奈哌齐形成相似的相互作用。因此,尼泊亭可能为开发治疗阿尔茨海默病等认知和记忆障碍的治疗剂提供线索。

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