首页> 外文会议>2010 3rd International Conference on Biomedical Engineering and Informatics >Effect of hesperidin extraction on cell proliferation and apoptosis of Alzheimer''s disease induced by Aβ25–35
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Effect of hesperidin extraction on cell proliferation and apoptosis of Alzheimer''s disease induced by Aβ25–35

机译:橙皮苷提取物对Aβ 25–35 诱导的阿尔茨海默病细胞增殖和凋亡的影响

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Objective: To study the effect of hesperidin extracted from the peel of Gannan kumquat on Alzheimer''s disease and its possible mechanisms. Methods: Cellular model of Alzheimer''s disease was established using PC12 cell induced by serum starvation method and treated by β-amyloid peptide 25–35 (Aβ25–35). Effect of hesperidin on proliferation of PC12 cell induced by Aβ25–35 was detected by the MTT method. Effect of hesperidin on apoptosis of PC12 cell induced by Aβ25–35 was utilized by the acridine orange / ethidium bromide staining method. Results: PC12 cells stayed at G0 stage induced by serum starvation method in order to simulate the neuron in the state of terminal differentiation. After this, the PC cells induced by serum atarvation were treated by Aβ25–35 to establish the cellular model of Alzheimer''s disease. After synchronized PC12 cells being pretreated with different concentrations of hesperidin (0–200 µmol/L) for 1 h, and then 30 µmol/L Aβ25–35 for 24 h, it was found that the survival rate increased along with the increasing dosage of hesperidin (F = 995.8,P < 0.001); however, there was no significant difference between 100 µmol/L group and 200 µmol/L group (P > 0.05). After synchronized PC12 cells being pretreated with 100µmol/L hesperidin for 1 h, and then 30 µmol/L Aβ25–35 for 24h, the cell nuclei were gradually similar to the cell nuclei of control group by by acridine orange/ethidium bromide fluorescent staining.Conclusion:Hesperidin inhibited the cytotoxicity and apoptosis induced by Aβ25–35 and had protection for neurocyte.
机译:目的:研究甘南金桔皮中橙皮苷的提取物对阿尔茨海默氏病的影响及其可能的机制。方法:利用血清饥饿法诱导的PC12细胞建立阿尔茨海默病细胞模型,并用β-淀粉样蛋白肽25-35(Aβ 25-35 )处理。 MTT法检测橙皮苷对Aβ 25–35 诱导的PC12细胞增殖的影响。 s啶橙/溴化乙锭染色法研究橙皮苷对Aβ 25–35 诱导的PC12细胞凋亡的影响。结果:血清饥饿法诱导PC12细胞停留在G 0 阶段,以模拟神经元处于终末分化状态。此后,用Aβ 25–35 处理血清成年诱导的PC细胞,以建立阿尔茨海默氏病的细胞模型。用不同浓度的橙皮素(0–200 µmol / L)预处理同步的PC12细胞1 h,然后用30 µmol / LAβ 25–35 预处理24 h后,发现其存活比率随着橙皮苷剂量的增加而增加(F = 995.8,P <0.001);然而,100 µmol / L组和200 µmol / L组之间没有显着差异(P> 0.05)。同步PC12细胞先用100μmol/ L橙皮苷预处理1 h,然后再用30μmol/ LAβ 25-35 预处理24h,然后,细胞核与对照组的细胞核逐渐相似。结论:橙皮苷抑制Aβ 25-35 诱导的细胞毒性和凋亡,并具有保护神经细胞的作用。

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