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6-扁桃酸及其糖苷可改善小鼠的记忆障碍。

6-Paradol and its glucoside improve memory disorder in mice.

机构信息

Graduate School of Natural Science and Technology, Gifu University, 1-1 Yanagido 501-1193, Gifu, Japan.

出版信息

Food Funct. 2020 Nov 18;11(11):9892-9902. doi: 10.1039/d0fo01975e.

Abstract

In this study, the effects of 6-paradol (6P) and 6-paradol-β-glucoside (6PG) on neuritogenesis were investigated using PC12 cells. Treatment with 200 μM 6P or 6PG and nerve growth factor (NGF) (5 ng mL-1) increased the number of elongated dendritic cells 8.7 and 5.4 times, respectively, compared to that with NGF (5 ng mL-1) treatment alone. 6P and 6PG did not stimulate the phosphorylation of extracellular regulated protein kinases (ERK)1/2 and cAMP response element-binding protein (CREB) in the tropomyosin receptor kinase A (TrkA) pathway as their activities were suppressed by the pathway inhibitor, k252a. 6P enhanced Ca2+ influx into the cells, whereas 6PG had no effect on Ca2+ influx, although it stimulated PC12 cell differentiation. High-performance liquid chromatography (HPLC) analysis of 6PG in PC12 culture medium suggested that 6PG was deglycosylated to generate 6P, which exhibited the effect. Furthermore, the bioactivities of 6P and 6PG were investigated in mice, and the results revealed that they ameliorated short-term memory loss in animals during behavioral testing.

摘要

在这项研究中,使用 PC12 细胞研究了 6-para-dol(6P)和 6-para-dol-β-葡萄糖苷(6PG)对神经突生成的影响。与单独使用神经生长因子(NGF)(5ng/ml-1)处理相比,用 200μM 6P 或 6PG 和神经生长因子(NGF)(5ng/ml-1)处理分别使伸长的树突状细胞的数量增加了 8.7 倍和 5.4 倍。6P 和 6PG 没有刺激丝氨酸/苏氨酸蛋白激酶 A(TrkA)途径中的细胞外调节蛋白激酶(ERK)1/2 和 cAMP 反应元件结合蛋白(CREB)的磷酸化,因为它们的活性被途径抑制剂 k252a 抑制。6P 增强了细胞内钙离子的流入,而 6PG 虽然刺激了 PC12 细胞分化,但对钙离子流入没有影响。高效液相色谱(HPLC)分析 PC12 培养基中的 6PG 表明,6PG 发生了去糖基化生成了 6P,后者表现出了这种作用。此外,还在小鼠中研究了 6P 和 6PG 的生物活性,结果表明它们在行为测试中改善了动物的短期记忆丧失。

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