Shen Yuh-Chiang, Juan Chi-Wen, Lin Che-San, Chen Chien-Chih, Chang Chia-Lin
National Research Institute of Chinese Medicine, Ministry of Health and Welfare, Taipei City, Taiwan (R.O.C.).
Institute of Biomedical Sciences, National Chung Hsing University, Taichung City, Taiwan (R.O.C.).
Afr J Tradit Complement Altern Med. 2017 Jun 5;14(4):22-30. doi: 10.21010/ajtcam.v14i4.3. eCollection 2017.
Alzheimer's disease (AD) is one of the common neurodegenerative disorders among elderly. The purpose of this study was to determine the neuroprotective effect and mechanisms of action underlying the extracts and ellagic acid by using beta-amyloid (Aβ)-induced cell toxicity in an undifferentiated pheochromocytoma (PC12) cell line.
The extracts were prepared using the methanol, water, and 95% ethanol. Specifically, the ellagic acid was obtained in our laboratory. Assays including cell toxicity and changes in intracellular reactive oxygen species (ROS) and calcium level were evaluated to examine the neuroprotective effects and mechanisms of the extracts and ellagic acid.
The methanolic and water extracts of and ellagic acid exhibited the strongest neuroprotective activity against Aβ-induced PC12 cell damages at 0.5-5.0 μg/ml. The ellagic acid also exhibited partial neuroprotective activity against HO-induced PC12 cell damages at 0.5-5.0 μg/ml. The methanolic and water extracts of and ellagic acid protected PC12 cells from Aβ-mediated cell damages and enhanced cell viability thorough two key mechanisms by: (1) inhibiting ROS production and (2) reducing calcium ion influx.
The represents a promising plant-source as medicine in the application for the treatment of AD. Further investigation focusing on the active component of extracts e.g., ellagic acid is crucial to verify the neuroprotective efficacy and mechanisms .
阿尔茨海默病(AD)是老年人常见的神经退行性疾病之一。本研究的目的是通过在未分化的嗜铬细胞瘤(PC12)细胞系中利用β-淀粉样蛋白(Aβ)诱导的细胞毒性,来确定提取物和鞣花酸的神经保护作用及其作用机制。
使用甲醇、水和95%乙醇制备提取物。具体而言,鞣花酸是在我们实验室获得的。通过评估包括细胞毒性以及细胞内活性氧(ROS)和钙水平变化等测定,来研究提取物和鞣花酸的神经保护作用及其机制。
提取物的甲醇提取物和水提取物以及鞣花酸在0.5 - 5.0μg/ml浓度下对Aβ诱导的PC12细胞损伤表现出最强的神经保护活性。鞣花酸在0.5 - 5.0μg/ml浓度下对过氧化氢(HO)诱导的PC12细胞损伤也表现出部分神经保护活性。提取物的甲醇提取物和水提取物以及鞣花酸通过两种关键机制保护PC12细胞免受Aβ介导的细胞损伤并提高细胞活力:(1)抑制ROS产生;(2)减少钙离子内流。
该提取物在治疗AD的应用中代表了一种有前景的植物源药物。进一步聚焦于提取物的活性成分如鞣花酸的研究对于验证神经保护功效及其机制至关重要。