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生物分子筛选 L. 对小鼠脑抗氧化和乙酰胆碱酯酶活性的影响。

Biomolecular Screening of L. for Antioxidant and Anticholinesterase Activity in Mice Brain.

机构信息

Department of Pharmaceutical Sciences, Government College University, Lahore 54000, Pakistan.

Gulab Devi Institute of Pharmacy, Gulab Devi Educational Complex, Lahore 54000, Pakistan.

出版信息

Molecules. 2023 Feb 27;28(5):2217. doi: 10.3390/molecules28052217.

Abstract

Hundreds of the plants have been explored and evaluated for antioxidant and anti-amnesic activities, so far. This study was designed to report the biomolecules of L. for the said activities. The aqueous extract of dried seeds was fractionated via column chromatography and the fractions so obtained were assessed for the inhibition of acetylcholinesterase (AChE) via in vitro analysis. The fraction which best inhibited AChE was so named as the active fraction (P.aAF). The P.aAF was then chemically analyzed via GCMS, which indicated that oxadiazole compounds were present in it. The P.aAF was then administered to albino mice to conduct the in vivo (behavioral and biochemical) studies. The results of the behavioral studies indicated the significant ( < 0.001) increase in inflexion ratio, by the number of hole-pokings through holes and time spent in a dark area by P.aAF treated mice. Biochemical studies demonstrated that the oxadiazole present in P.aAF on one hand presented a noteworthy reduction in MDA and the AChE level and on the other hand promoted the levels of CAT, SOD and GSH in mice brain. The LD for P.aAF was calculated as 95 mg/Kg/p.o. The findings thus supported that the antioxidant and anticholinesterase activities of are due to its oxadiazole compounds.

摘要

迄今为止,已有数百种植物因其抗氧化和抗健忘活性而被探索和评估。本研究旨在报告 L. 的生物分子具有所述活性。通过柱层析对干燥 种子的水提取物进行分级,所得各馏分通过体外分析评估对乙酰胆碱酯酶(AChE)的抑制作用。对 AChE 抑制作用最佳的馏分被命名为 活性馏分(P.aAF)。然后通过 GCMS 对 P.aAF 进行化学分析,结果表明其中存在恶二唑化合物。然后将 P.aAF 给予白化病小鼠进行体内(行为和生化)研究。行为研究的结果表明,P.aAF 处理的小鼠通过孔刺的次数和在暗区停留的时间的转弯比有显著(<0.001)增加。生化研究表明,P.aAF 中存在的恶二唑一方面显著降低 MDA 和 AChE 水平,另一方面促进了 CAT、SOD 和 GSH 在小鼠大脑中的水平。P.aAF 的 LD 计算为 95 mg/Kg/p.o。因此,研究结果支持 的抗氧化和抗胆碱酯酶活性归因于其恶二唑化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6964/10005257/0e32a7618da8/molecules-28-02217-g001.jpg

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