Master of Science Program in Toxicology and Nutrition for Food Safety, Institute of Nutrition, Mahidol University, Salaya, Phuttamonthon, Nakhon Pathom 73170, Thailand.
Institute of Nutrition, Mahidol University, Salaya, Phuttamonthon, Nakhon Pathom 73170, Thailand.
Molecules. 2024 May 8;29(10):2204. doi: 10.3390/molecules29102204.
A previous study reported that the ethanolic extract of the edible fern, (Retz.) Sw. (DE), obtained from a non-optimized extraction condition exhibited anti-Alzheimer's disease (AD) properties through the inhibition of a rate-limiting enzyme in amyloid peptide formation, β-secretase-1 (BACE-1). Nevertheless, a non-optimized or suboptimal extraction may lead to several issues, such as a reduction in extraction efficiency and increased time and plant materials. In this study, extraction of the DE was optimized to obtain appropriate BACE-1 inhibition using a Box-Behnken design (BBD) and response surface methodology (RSM). Data revealed that the optimal extraction condition was 70% (/) aqueous ethanol, 50 min extraction time, 30 °C extraction temperature, and 1:30 g/mL solid/liquid ratio, giving BACE-1 inhibition at 56.33%. In addition, the extract also exhibited significant antioxidant activities compared to the non-optimized extraction. Metabolomic phytochemical profiles and targeted phytochemical analyses showed that kaempferol, quercetin, and their derivatives as well as rosmarinic acid were abundant in the extract. The optimized DE extract also acted synergistically with donepezil, an AD drug suppressing BACE-1 activities. Data received from -expressing human amyloid precursor proteins (APPs) and BACE-1, representing the amyloid hypothesis, showed that the optimized DE extract penetrated the fly brains, suppressed BACE-1 activities, and improved locomotor functions. The extract quenched the expression of glutathione S transferase D1 (GSTD1), inositol-requiring enzyme (IRE-1), and molecular chaperone-binding immunoglobulin (Bip), while donepezil suppressed these genes and other genes involved in antioxidant and endoplasmic reticulum (ER) stress response, including superoxide dismutase type 1 (SOD1), activating transcription factor 6 (ATF-6), and protein kinase R-like endoplasmic reticulum kinase (PERK). To sum up, the optimized extraction condition reduced extraction time while resulting in higher phytochemicals, antioxidants, and BACE-1 inhibitors.
先前的研究报告称,从非优化提取条件下获得的食用蕨类植物(Retz.)Sw.(DE)的乙醇提取物通过抑制淀粉样肽形成的限速酶β-分泌酶-1(BACE-1)表现出抗阿尔茨海默病(AD)的特性。然而,非优化或次优提取可能会导致几个问题,例如提取效率降低、提取时间延长和植物材料增加。在这项研究中,使用 Box-Behnken 设计(BBD)和响应面法(RSM)对 DE 的提取进行了优化,以获得适当的 BACE-1 抑制作用。数据显示,最佳提取条件为 70%(/)水性乙醇、50 分钟提取时间、30°C 提取温度和 1:30 g/mL 固液比,BACE-1 抑制率为 56.33%。此外,与非优化提取相比,提取物还表现出显著的抗氧化活性。代谢组学植物化学特征和靶向植物化学分析表明,槲皮素、山柰酚及其衍生物以及迷迭香酸在提取物中含量丰富。与 AD 药物多奈哌齐(抑制 BACE-1 活性)协同作用的优化 DE 提取物。从表达人淀粉样前体蛋白(APPs)和 BACE-1 的转基因果蝇中获得的数据,代表淀粉样蛋白假说,表明优化后的 DE 提取物穿透果蝇大脑,抑制 BACE-1 活性,改善运动功能。提取物抑制了谷胱甘肽 S 转移酶 D1(GSTD1)、肌醇需求酶(IRE-1)和分子伴侣结合免疫球蛋白(Bip)的表达,而多奈哌齐抑制了这些基因和其他参与抗氧化和内质网(ER)应激反应的基因,包括超氧化物歧化酶 1(SOD1)、激活转录因子 6(ATF-6)和蛋白激酶 R 样内质网激酶(PERK)。总之,优化的提取条件减少了提取时间,同时产生了更高的植物化学物质、抗氧化剂和 BACE-1 抑制剂。