Sui Zifang, Qi Ce, Huang Yunxiang, Ma Shufeng, Wang Xinguo, Le Guowei, Sun Jin
The Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi214122, China.
Food Funct. 2017 Apr 19;8(4):1460-1467. doi: 10.1039/c7fo00028f.
Aqueous extracts from Asparagus officinalis L. stems (AEAS) are rich in polysaccharides, gamma-amino butyric acid (GABA), and steroidal saponin. This study was designed to investigate the effects of AEAS on learning, memory, and acetylcholinesterase-related activity in a scopolamine-induced model of amnesia. Sixty ICR mice were randomly divided into 6 groups (n = 10) including the control group (CT), scopolamine group (SC), donepezil group (DON), low, medium, and high dose groups of AEAS (LS, MS, HS; 1.6 mL kg, 8 mL kg, 16 mL kg). The results showed that 8 mL kg of AEAS used in this study significantly reversed scopolamine-induced cognitive impairments in mice in the novel object recognition test (P < 0.05) and the Y-maze test (P < 0.05), and also improved the latency to escape in the Morris water maze test (P < 0.05). Moreover, it significantly increased acetylcholine and inhibited acetylcholinesterase activity in the hippocampus, which was directly related to the reduction in learning and memory impairments. It also reversed scopolamine-induced reduction in the hippocampal brain-derived neurotrophic factor (BDNF) and the cAMP response element-binding protein (CREB) mRNA expression. AEAS protected against scopolamine-induced memory deficits. In conclusion, AEAS protected learning and memory function in mice by enhancing the activity of the cholinergic nervous system, and increasing BDNF and CREB expression. This suggests that AEAS has the potential to prevent cognitive impairments in age-related diseases, such as Alzheimer's disease.
芦笋茎水提取物(AEAS)富含多糖、γ-氨基丁酸(GABA)和甾体皂苷。本研究旨在探讨AEAS对东莨菪碱诱导的失忆模型中学习、记忆及乙酰胆碱酯酶相关活性的影响。将60只ICR小鼠随机分为6组(n = 10),包括对照组(CT)、东莨菪碱组(SC)、多奈哌齐组(DON)、AEAS低、中、高剂量组(LS、MS、HS;1.6 mL/kg、8 mL/kg、16 mL/kg)。结果显示,本研究中使用的8 mL/kg AEAS在新颖物体识别试验(P < 0.05)和Y迷宫试验(P < 0.05)中显著逆转了东莨菪碱诱导的小鼠认知障碍,并且在莫里斯水迷宫试验中改善了逃避潜伏期(P < 0.05)。此外,它显著增加了海马中的乙酰胆碱并抑制了乙酰胆碱酯酶活性,这与学习和记忆障碍的减轻直接相关。它还逆转了东莨菪碱诱导的海马脑源性神经营养因子(BDNF)和cAMP反应元件结合蛋白(CREB)mRNA表达的降低。AEAS可预防东莨菪碱诱导的记忆缺陷。总之,AEAS通过增强胆碱能神经系统的活性以及增加BDNF和CREB的表达来保护小鼠的学习和记忆功能。这表明AEAS具有预防与年龄相关疾病(如阿尔茨海默病)中认知障碍的潜力。