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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:利用RSM优化PRG(一种来自桑黄的多糖)的降解条件并优化Aβ25–35损伤PC12细胞的神经保护活性

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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是一种来自桑黄的多糖,具有神经营养活性。为了获得具有较低分子量的活性结构单元,使用抗坏血酸和过氧化氢将PRG降解以制备降解的PRG(DPRG)。本文的目的是通过使用响应表面方法(RSM)优化降解条件来获得DPRG,并研究其对Aβ25-35诱导的PC12细胞的保护作用。最佳条件如下: H 2 O 2 -Vc的浓度为17mM,降解温度为50℃。当降解时间为1.6 h时,PC12细胞活力的实验响应值为83.4±0.15%,与预测值(83.5%)一致。我们还研究了DPRG对Aβ25-35诱导的神经毒性的保护作用,并探讨了其潜在机制。结果表明,用DPRG处理可以减轻PC12细胞的死亡。该机制与通过增加PC12细胞中的MMP水平和降低细胞色素C(Cytc)的蛋白表达来抑制细胞凋亡有关。结论成功地获得了较低分子量的DPRG。它具有神经保护特性,可能是神经退行性疾病治疗的候选者。

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