首页> 外文期刊>Radiology >Peripheral nerve repair: monitoring by using gadofluorine M-enhanced MR imaging with chitosan nerve conduits with cultured mesenchymal stem cells in rat model of neurotmesis.
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Peripheral nerve repair: monitoring by using gadofluorine M-enhanced MR imaging with chitosan nerve conduits with cultured mesenchymal stem cells in rat model of neurotmesis.

机译:周围神经修复:使用加多氟胺M增强的MR成像与壳聚糖神经导管以及培养的间充质干细胞在神经分裂症大鼠模型中进行监测。

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PURPOSE: To observe the longitudinal changes of nerve repair in rats after tissue-engineered construct implantation at magnetic resonance (MR) imaging and to determine whether the enhanced nerve regeneration with use of tissue-engineered constructs could be monitored with gadofluorine M-enhanced MR imaging or nerve T2 relaxation time measurement. MATERIALS AND METHODS: All experimental protocols were approved by the institutional Animal Use and Care Committee. Tissue-engineered constructs were prepared by seeding mesenchymal stem cells (MSCs) into chitosan nerve tubes. Thirty-six rats with sciatic nerve transection injury underwent nerve tube implantation with (n = 18) or without (n = 18) MSC seeding. Sequential T2 measurement, gadofluorine M-enhanced MR imaging, and sciatic function index measurement were performed over an 8-week follow-up period, with histologic assessments performed at regular intervals. T2 relaxation times and signal intensity at gadofluorine M-enhanced T1-weighted imaging were measured and were compared by using repeated-measures analysis of variance followed by the Student-Neuman-Keuls post-hoc test for multiple pairwise comparisons. RESULTS: Nerve T2 relaxation times and gadofluorine M enhancement, as well as functional changes, showed a similar time course. Nerves implanted with MSC-seeded tubes achieved slightly better functional recovery and enhanced nerve regeneration while showing a slower return to baseline T2 relaxation time and a more rapid decline in gadofluorine M enhancement compared with nerves implanted with chitosan tubes alone. T2 values of the distal portion of transected nerves showed a more rapid return to baseline level than did gadofluorine M enhancement. CONCLUSION: Peripheral nerve repair with use of tissue-engineered constructs can be monitored by using gadofluorine M-enhanced MR imaging and T2 relaxation time measurements. T2 relaxation time seems more sensitive than gadofluorine M-enhanced MR imaging for detecting nerve regeneration.
机译:目的:观察组织工程植入物在磁共振(MR)成像后大鼠神经修复的纵向变化,并确定是否可以通过g荧光增强M MR监测使用组织工程构建物的神经再生增强或神经T2放松时间的测量。材料与方法:所有实验方案均已获得动物保护与使用委员会的批准。通过将间充质干细胞(MSCs)植入壳聚糖神经管中来制备组织工程构建体。坐骨神经横断损伤的三十六只大鼠植入神经管植入(n = 18)或不植入(n = 18)MSC。在为期8周的随访期内,进行了连续的T2测量,M氟M增强MR成像以及坐骨神经功能指数测量,并定期进行组织学评估。测量并用g氟M增强的T1加权成像测量T2弛豫时间和信号强度,并使用方差重复测量分析,然后通过Student-Neuman-Keuls post-hoc检验进行多次成对比较,并进行比较。结果:神经T2放松时间和g氟M增强以及功能变化显示出相似的时间过程。与仅植入壳聚糖管的神经相比,植入MSC种子管的神经获得了更好的功能恢复,并增强了神经再生,同时显示出较慢的恢复到基线T2弛豫时间,并且降低了gadofluorine M增强。横断神经末梢的T2值显示比加多氟醚M增强更快返回基线水平。结论:通过使用g荧光的M增强MR成像和T2弛豫时间测量,可以监测使用组织工程结构的周围神经修复。对于检测神经再生,T2弛豫时间似乎比用ado荧光增强M增强的MR成像更为敏感。

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