College of Food Science & Nutritional Engineering, China Agricultural University, No. 17 Tsinghua Dong Road, Beijing 100083, China.
Institute of Nutrition and Health, Qingdao University, 308 Ningxia Road, Qingdao 266071, China.
Food Funct. 2021 Nov 1;12(21):10994-11008. doi: 10.1039/d1fo02122b.
Cyanidin 3--galactoside (Cy3Gal) from has been reported to alleviate cognitive impairment. Metformin for preventing the neurodegenerative disease is attracting increasing attention. However, the neuroprotective and metabolic health promoting both of their effects are not clear. We chose the senescence accelerated mouse prone 8 (SAMP8) as a model of spontaneous learning and memory impairment. This study aimed to investigate the synergistic neuroprotective effect of metformin and Cy3Gal by behavioral and histopathological assays and metabolite analysis in SAMP8 mice. The SAMR1 mice were the normal group, and the SAMP8 mice were divided into five groups, including the SAMP8 model group, the donepezil (1 mg kg, ig) group, the metformin (100 mg kg, ig) group, the Cy3Gal (25 mg kg, ig) group, and the combination of metformin plus Cy3Gal (Met + Cy3Gal, 100 mg kg, 25 mg kg, ig) group. The behavior experiments showed that the SAMP8 mice treated with metformin and Cy3Gal showed improved spatial learning and memory compared to the SAMP8 model group. The number of neurons in the Met + Cy3Gal group was significantly higher than that in the SAMP8 group and the Met + Cy3Gal group showed significantly reduced Aβ aggregation in the brain, which was elevated in SAMP8 mice. Compared with SAMP8 mice, the Met + Cy3Gal group showed decreased indole, methyl esters and ketones and increased short-chain fatty acids and alcohols in feces and urine by regulating the fatty acid biosynthesis and degradation. This study confirmed the neuroprotective effects of coadministration of metformin and cyanidin 3--galactoside in the SAMP8 mice, and suggested its positive effect on postponing the progression of Alzheimer's disease.
矢车菊素 3-半乳糖苷(Cy3Gal)已被报道可减轻认知障碍。二甲双胍预防神经退行性疾病越来越受到关注。然而,其神经保护和代谢健康促进作用尚不清楚。我们选择衰老加速小鼠 prone 8(SAMP8)作为自发学习和记忆障碍的模型。本研究旨在通过行为和组织病理学检测以及代谢物分析,研究二甲双胍和 Cy3Gal 对 SAMP8 小鼠的协同神经保护作用。SAMR1 小鼠为正常组,SAMP8 小鼠分为 SAMP8 模型组、多奈哌齐(1mg/kg,ig)组、二甲双胍(100mg/kg,ig)组、Cy3Gal(25mg/kg,ig)组和二甲双胍加 Cy3Gal(Met+Cy3Gal,100mg/kg,25mg/kg,ig)组。行为学实验表明,与 SAMP8 模型组相比,用二甲双胍和 Cy3Gal 处理的 SAMP8 小鼠表现出空间学习和记忆能力提高。Met+Cy3Gal 组的神经元数量明显高于 SAMP8 组,Met+Cy3Gal 组脑内 Aβ 聚集明显减少,SAMP8 小鼠脑内 Aβ 聚集增加。与 SAMP8 小鼠相比,Met+Cy3Gal 组通过调节脂肪酸生物合成和降解,使粪便和尿液中的吲哚、甲酯和酮减少,短链脂肪酸和醇增加。本研究证实了二甲双胍和矢车菊素 3-半乳糖苷联合应用于 SAMP8 小鼠的神经保护作用,并提示其对延缓阿尔茨海默病进展有积极作用。