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Fuzheng Quxie Decoction Ameliorates Learning and Memory Impairment in SAMP8 Mice by Decreasing Tau Hyperphosphorylation

机译:扶正祛邪汤通过降低Tau蛋白的过度磷酸化来减轻SAMP8小鼠的学习和记忆障碍

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摘要

Hyperphosphorylation of the microtubule-associated protein, tau, is critical to the progression of Alzheimer's disease (AD). Fuzheng Quxie Decoction (FQD), a Chinese herbal complex, is an effective clinical formula used to treat AD. In the current study, we employed high-performance liquid chromatography and liquid chromatography tandem mass spectrometry to identify the components of FQD. Three major components (ginsenoside Rg1, ginsenoside Re, and coptisine) were detected in the brain of FQD-fed mice, indicating their ability to cross the blood-brain barrier. We further evaluated the efficacy of FQD on Senescence-Accelerated Mice Prone-8 (SAMP8) mice. FQD significantly ameliorated learning and memory deficits in SAMP8 mice on the Morris Water Maze, decreasing escape latency (p < 0.01) and increasing swim time within the original platform-containing quadrant (p < 0.05). Further, FQD increased the number of neurons and intraneuronal Nissl bodies in the hippocampal CA1 region. FQD also decreased the expression of phosphorylated tau protein and increased the expression of protein phosphatase 2A (PP2A) and the N-methyl-D-aspartate receptor subunit, NR2A (p < 0.01). Our results indicate that FQD improves the learning and memory ability of SAMP8 mice. Moreover, our findings suggest that the protective effect of FQD is likely mediated through an inhibition of hippocampal tau hyperphosphorylation via NMDAR/PP2A-associated proteins.
机译:微管相关蛋白tau的过度磷酸化对阿尔茨海默氏病(AD)的进展至关重要。扶正祛邪汤(FQD)是一种中草药复合物,是一种有效的治疗AD的临床配方。在当前的研究中,我们采用了高效液相色谱和液相色谱串联质谱法来鉴定FQD的成分。在FQD喂养的小鼠的大脑中检测到三个主要成分(人参皂甙Rg1,人参皂甙Re和黄连碱),表明它们具有穿越血脑屏障的能力。我们进一步评估了FQD对衰老加速小鼠易感8(SAMP8)小鼠的疗效。 FQD显着改善了莫里斯水迷宫(Morris Water Maze)上SAMP8小鼠的学习和记忆缺陷,减少了逃逸潜伏期(p <0.01),并增加了在原始平台含象限内的游泳时间(p <0.05)。此外,FQD增加了海马CA1区神经元和神经内尼氏体的数量。 FQD还降低了磷酸化tau蛋白的表达,并增加了蛋白磷酸酶2A(PP2A)和N-甲基-D-天冬氨酸受体亚基NR2A的表达(p <0.01)。我们的结果表明FQD可以提高SAMP8小鼠的学习和记忆能力。此外,我们的研究结果表明FQD的保护作用可能是通过抑制NMDAR / PP2A相关蛋白对海马tau蛋白过度磷酸化的介导的。

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