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作 者:李学东[1] 邓志云 陈斌[1] 郑创义[1] 刘钊勇[1] 熊华花[3] 杜世新[1]
机构地区:[1]汕头大学医学院第一附属医院骨科,广东515041 [2]广东省边防武警总队医院外科 [3]深圳市第二人民医院超声科
出 处:《中华手外科杂志》2009年第3期161-164,共4页Chinese Journal of Hand Surgery
摘 要:目的制备β-神经生长因子(nerve growth factor,NGF)缓释系统,评价其及其组份对体外培养鸡胚背根神经节(dorsal root ganglion,DRG)轴突生长的生物学效应。方法构建含pNGF50、100、250μg/L的缓释系统分别与DRG共同培养,DRG常规培养作为对照组,了解各浓度组DRG的轴突生长;分别利用缓释系统各组份与DRG培养,观察各组轴突生长情况。实验分成6组:对照组(DRG+纤维蛋白原),A组(DRG+纤维蛋白原+肝素结合肽+肝素钠+100μg/Lβ-NGF),B组(DRG+纤维蛋白原+肝素钠+100μg/Lβ-NGF),C组(DRG+纤维蛋白原+肝素结合肽+100μg/Lβ-NGF),D组(DRG+纤维蛋白原+100μg/Lβ-NGF),E组(DRG+纤维蛋白原+肝素结合肽+肝素钠)。结果50、1130和250μg/Lβ-NGF缓释系统轴突生长是对照组的1.31(P〉0.05)、3.78(P〈0.01)和3.05(P〈0.01)倍;100μg/L组较250μg/L组DRG轴突生长明显(P〈0.05)。实验组A、B、C、D和E组的DRG轴突生长分别是对照组的3.75、1.15、1.12、1.10和1.09倍,与对照组比较仅A组差异有统计学意义(P〈0.01)。结论β-NGF缓释系统中释放的β-NGF具有生物活性,可明显促进DRG轴突生长。Objective To construct β-NGF controlled delivery system and evaluate the biological effects of β-NGF on the growth of chick embryo dorsal root ganglion (DRG) axons in vitro. Methods Delivery systems releasing β-NGF at 50 μg/L, 100 μg/L and 250μg/L concentration were constructed. To determine the optimal dose response effects of NGF in the controlled delivery system, DRG were co-cultured with of β-NGF at above concentrations while using DRG basic culture as control. Axonal growth was observed. DRG were also co-cultured with the components in the controlled delivery system to detect the effects on growth of DRG axons. The experiment was divided into 5 experimental groups and 1 control group: control group, DRG + fibrin; Group A, DRG+ fibrin+ peptide + heparin + 100μ/L β+NGF; Group B, DRG+ fibrin+ heparin + 100μg/L β-NGF; Group C, DRG + fibrin + peptide + 100 μg/L β-NGF; Group D, DRG + fibrin + 100 μg/L β-NGF; Group E, DRG + fibrin + peptide + heparin. Results The growth of DRG axons in 50 μg/L, 100μg/L and 250μg/L concentration of β-NGF controlled delivery system was 1.31 ( P 〉 0.05), 3.78 ( P 〈 0. 01 ) and 3.05 ( P 〈 0.01) folds of the control respectively. The growth of DRG axons in 100 μg/L group was significantly better comparing to that in 250μg/L group. The grouh of DRG axons in Groups A, B, C, D and E was 3.75, 1.15, 1.12, 1.10 and 1.09 folds of the control group, respoctively. The difference was only statistically significant between Group A and the control group ( P 〈 0.01 ). Conclusion β-NGF released from the β-NGF controlled delivery system was bioactive. It could promote the growth of DRG axons.
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