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Evoked thalamic neuronal activity following DRG application of two nucleus pulposus derived cell populations: an experimental study in rats

机译:DRG应用两个髓核衍生细胞群后诱发的丘脑神经元活性:在大鼠中的实验研究

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PurposeTo investigate the effects on evoked thalamic neuronal activity of application of notochordal cells and chondrocyte-like cells derived from nucleus pulposus (NP) onto a dorsal root ganglion (DRG) and to compare these effects with a previously reported increased thalamic activity induced by NP.MethodsNucleus pulposus was harvested from tail discs of adult rats and the disc cells were separated into two cell populations, notochordal cells and chondrocyte-like cells. The two cell populations were applied separately, or in combination, to the L4 DRG of anaesthetised female Sprague–Dawley rats during acute electrophysiological experiments. In control experiments, cell suspension medium was applied on the DRG. Recordings from the contralateral thalamus were sampled for 40?min while electrically stimulating the ipsilateral sciatic nerve at above Aδ-fibre thresholds.ResultsApplication of notochordal cells resulted in a decrease in evoked thalamic activity within 10?min while chondrocyte-like cells did not induce any changes during the 40?min of recording. The difference in evoked thalamic activity 40?min after notochordal and chondrocyte-like cell application, respectively, was statistically significant. Neither an increased concentration of chondrocyte-like cells alone nor a combination of the two cell populations induced any changes in thalamic activity.ConclusionsSeparate exposure of the DRG to the two NP-derived cell populations induced different effects on evoked thalamic activity, but none of the tested cell samples induced an increase in neuronal activity similar to that previously observed with NP. This indicates a high complexity of the interaction between NP and nervous tissue...
机译:目的研究将髓核(NP)的脊索细胞和软骨细胞样细胞应用于背根神经节(DRG)对诱发的丘脑神经元活性的影响,并将这些影响与先前报道的由NP诱导的丘脑活性增加进行比较。方法从成年大鼠尾椎间盘摘取髓核,并将其分离为两个细胞群,即脊索细胞和软骨细胞样细胞。在急性电生理实验中,将两种细胞群分别或组合应用于麻醉的雌性Sprague-Dawley大鼠的L4 DRG。在对照实验中,将细胞悬浮培养基施加到DRG上。对侧丘脑的记录采样40分钟,同时以高于Aδ纤维的阈值电刺激同侧坐骨神经。结果应用脊索细胞可导致10分钟内丘脑活动度降低,而软骨样细胞则未诱导任何刺激在录制40分钟内发生变化。分别应用脊索细胞和软骨细胞样细胞后40?min诱发的丘脑活性的差异具有统计学意义。单独增加软骨细胞样细胞的浓度或两个细胞群的组合都不会引起丘脑活性的任何变化。结论将DRG分别暴露于两个NP衍生的细胞群不会引起对诱发的丘脑活性的不同影响,但没有一个被测细胞样品诱导的神经元活性增加,类似于先前用NP观察到的。这表明NP和神经组织之间相互作用的高度复杂性。

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