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首页> 外文期刊>Revista Brasileira de Farmacognosia >Acetylcholinesterase inhibitory activity of a neurosteroidal alkaloid from the upside-down jellyfish Cassiopea andromeda venom
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Acetylcholinesterase inhibitory activity of a neurosteroidal alkaloid from the upside-down jellyfish Cassiopea andromeda venom

机译:上下颠倒的水母仙后座蛇毒中神经甾体生物碱的乙酰胆碱酯酶抑制活性

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摘要

Natural compounds from marine organisms have been rarely studied for their acetylcholinesterase inhibitory activities. The aim of this study was to isolate novel compounds with antiAChE activity from the venom of upside-down jellyfish Cassiopea andromeda Forsk?l, 1775. The compounds of the fractionated venom on gel filtration chromatography were identified by analyzing gas chromatography–mass spectroscopy data. The structure of the isolated compound that showed the most potent antiAChE activity in a docking study was elucidated by different spectral data, including 1 H NMR and 13 C NMR. Three compounds, including a neurosteroidal alkaloid androtoxin B, were identified from two venom fractions. This neurosteroidal alkaloid showed strong acetylcholinesterase inhibitory activity (IC 50 2.24 ± 0.1 μM) compared with the reference standard, galantamine. The results obtained by a docking study demonstrated that Androtoxin B had close contact with two of the three amino acid residues of the catalytic triad of acetylcholinesterase gorge and was accommodated within a peripheral hydrophobic pocket composed of numerous aromatic site chains. In conclusion, the isolated neurosteroidal alkaloid from Cassiopea andromeda was a potent antiAChE agent with strong binding to both the catalytic and peripheral sites of acetylcholinesterase that correlated well with the experimental data. Further studies are required to determine whether androtoxin B could be a potential treatment for Alzheimer's disease.
机译:很少研究海洋生物的天然化合物的乙酰胆碱酯酶抑制活性。这项研究的目的是从倒置的水母Cassiopea andromeda Forsk?l的毒液中分离出具有抗AChE活性的新型化合物,1775年。通过分析气相色谱-质谱数据,鉴定了凝胶过滤色谱法上分离出的蛇毒化合物。通过对接的光谱数据(包括1 H NMR和13 C NMR)阐明了在对接研究中显示出最有效的抗AChE活性的分离化合物的结构。从两个毒液组分中鉴定出三种化合物,包括神经甾体生物碱和毒素B。与参考标准加兰他敏相比,这种神经甾体生物碱具有很强的乙酰胆碱酯酶抑制活性(IC 50 2.24±0.1μM)。通过对接研究获得的结果表明,Androtoxin B与乙酰胆碱酯酶峡谷的催化三联体的三个氨基酸残基中的两个紧密接触,并被容纳在由许多芳香位点链组成的外围疏水口袋中。总之,从仙后座中提取的神经甾体生物碱是一种有效的抗AChE剂,与乙酰胆碱酯酶的催化位点和外围位点都具有很强的结合力,与实验数据具有很好的相关性。需要进一步的研究以确定雄激素B是否可以作为阿尔茨海默氏病的潜在治疗方法。

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