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Optimization of Degradation Conditions with PRG, a Polysaccharide from Phellinus ribis, by RSM and the Neuroprotective Activity in PC12 Cells Damaged by Aβ25–35

机译:用Phellinus Ribis的PRG,PROM和PC12细胞中的多糖的降解条件优化,PC12细胞中Aβ25-35受损的神经保护活性

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摘要

In the previous work, we found PRG, a polysaccharide from Phellinus ribis, exhibited neurotrophic activity. To obtain an active structural unit with lower molecular weight, PRG was degraded to prepare the degraded PRG (DPRG) using ascorbic acid and H2O2. The aim of the paper was to obtain DPRG by optimizing the degradation conditions using response surface methodology (RSM) and to study its protective effects of PC12 cells induced by Aβ25−35. The optimum conditions were as follows; the concentration of H2O2-Vc was 17 mM and degradation temperature was 50 °C; when degradation time was 1.6 h, the experimental response value of PC12 cell viability was 83.4 ± 0.15%, which was in accordance with the predicted value (83.5%). We also studied the protective effects of DPRG against the Aβ25−35-induced neurotoxicity and explored the underlying mechanism. The results showed that treatment with DPRG could attenuate PC12 cells death. The mechanism was relative to the inhibition of cell apoptosis by increasing the MMP level and decreasing the protein expression of cytochrome C (Cytc) in PC12 cells. In conclusion, DPRG with lower molecular weight was obtained successfully. It possessed neuroprotective properties and might be a candidate for neurodegenerative disease treatment.
机译:在以前的工作中,我们发现PRG,来自Phellinus Ribis的多糖,表现出神经营养活性。为了获得具有较低分子量的活性结构单元,降解PRG以制备使用抗坏血酸和H 2 O 2的降解的PRG(DPRG)。本文的目的是通过使用响应表面方法(RSM)优化降解条件并研究其β25-35诱导的PC12细胞的保护作用来获得DPRG。最佳条件如下; H 2 O 2-Vc的浓度为17mm,降解温度为50℃;当劣化时间为1.6小时时,PC12细胞活力的实验响应值为83.4±0.15%,这符合预测值(83.5%)。我们还研究了DPRG对Aβ25-35诱导的神经毒性的保护作用,并探索了潜在机制。结果表明,用DPRG治疗可以衰减PC12细胞死亡。通过增加MMP水平并降低PC12细胞中细胞色素C(CYTC)的细胞色素C(CYTC)的蛋白质表达来相对于细胞凋亡的抑制作用。总之,成功获得了分子量较低的DPRG。它具有神经保护性能,并且可能是神经变性疾病治疗的候选者。

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