首页> 美国卫生研究院文献>other >Antiaggregation Potential of Padina gymnospora against the Toxic Alzheimer’s Beta-Amyloid Peptide 25–35 and Cholinesterase Inhibitory Property of Its Bioactive Compounds
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Antiaggregation Potential of Padina gymnospora against the Toxic Alzheimer’s Beta-Amyloid Peptide 25–35 and Cholinesterase Inhibitory Property of Its Bioactive Compounds

机译:Padina Gymnospora对有毒阿尔茨海默氏β-淀粉样肽25-35的抗聚集潜力及其生物活性化合物的胆碱酯酶抑制特性

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摘要

Inhibition of β-amyloid (Aβ) aggregation in the cerebral cortex of the brain is a promising therapeutic and defensive strategy in identification of disease modifying agents for Alzheimer’s disease (AD). Since natural products are considered as the current alternative trend for the discovery of AD drugs, the present study aims at the evaluation of anti-amyloidogenic potential of the marine seaweed Padina gymnospora. Prevention of aggregation and disaggregation of the mature fibril formation of Aβ 25–35 by acetone extracts of P. gymnospora (ACTPG) was evaluated in two phases by Thioflavin T assay. The results were further confirmed by confocal laser scanning microscopy (CLSM) analysis and Fourier transform infrared (FTIR) spectroscopic analysis. The results of antiaggregation and disaggregation assay showed that the increase in fluorescence intensity of aggregated Aβ and the co-treatment of ACTPG (250 μg/ml) with Aβ 25–35, an extensive decrease in the fluorescence intensity was observed in both phases, which suggests that ACTPG prevents the oligomers formation and disaggregation of mature fibrils. In addition, ACTPG was subjected to column chromatography and the bioactivity was screened based on the cholinesterase inhibitory activity. Finally, the active fraction was subjected to LC-MS/MS analysis for the identification of bioactive compounds. Overall, the results suggest that the bioactive compound alpha bisabolol present in the alga might be responsible for the observed cholinesterase inhibition with the IC50 value < 10 μg/ml for both AChE and BuChE when compared to standard drug donepezil (IC50 value < 6 μg/ml) and support its use for the treatment of neurological disorders.
机译:在确定阿尔茨海默氏病(AD)的疾病改良剂时,抑制大脑皮质中的β-淀粉样蛋白(Aβ)聚集是一种有前途的治疗和防御策略。由于天然产物被认为是发现AD药物的当前替代趋势,因此本研究旨在评估海洋紫菜Padina Gymnospora的抗淀粉样蛋白生成潜力。通过硫黄素T分析分两个阶段评估了体育裸孢菌丙酮提取物(ACTPG)防止Aβ25-35成熟原纤维形成的聚集和解聚。共聚焦激光扫描显微镜(CLSM)分析和傅里叶变换红外(FTIR)光谱分析进一步证实了结果。抗聚集和解聚试验的结果表明,聚集的Aβ的荧光强度增加,ACTPG(250μg/ ml)与Aβ25-35共同处理,两个阶段的荧光强度均大大降低,这表明提示ACTPG可以防止寡聚体的形成和成熟原纤维的分解。另外,对ACTPG进行柱色谱,并根据胆碱酯酶抑制活性筛选生物活性。最后,将活性级分进行LC-MS / MS分析,以鉴定生物活性化合物。总体而言,结果表明,与标准药物多奈哌齐相比,藻类中存在的生物活性化合物α没药醇可能是所观察到的胆碱酯酶抑制作用的AChE和BuChE的IC50值均<10μg/ ml。毫升),并支持其用于治疗神经系统疾病。

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