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Effect of rat spinal cord injury (hemisection) on the ex vivo uptake and release of [3H]noradrenaline from a slice preparation

机译:大鼠脊髓损伤(半切)对切片制剂中[3H]去甲肾上腺素的离体吸收和释放的影响

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摘要

We measured the ex vivo uptake and release of [3H]noradrenaline ([3H]NA) from perfused rat spinal cord slice preparations at 1, 3 and 14days after unilateral hemisection-induced spinal cord injury (SCI) compared with control slice preparations. After surgical hemisection under anaesthesia, the rats showed characteristic signs of hemiplegia, with no movement of the ipsilateral hindlimb. After 3days, the electron microscopy images showed overall degeneration of neuronal organelles and the myelin sheath, but the synapses seemed to be intact. In ex vivo experiments, the spinal cord injury did not influence uptake but increased [3H]NA release at rest and in response to axonal stimulation. The effect of a selective noradrenaline reuptake inhibitor, nisoxetine, was studied to identify the mechanisms underlying the increase in NA release. Nisoxetine potentiated stimulation-evoked [3H]NA release from the non-injured tissue, but it gradually lost its effectiveness after injury, depending on the time (1 and 3days) elapsed after hemisection, indicating that the noradrenaline transporter binding sites of the terminals become impaired after decentralisation.
机译:我们与对照切片制剂相比,在单侧半切诱导的脊髓损伤(SCI)后第1、3和14天测量了灌注的大鼠脊髓切片制剂中[3H]去甲肾上腺素([3H] NA)的离体吸收和释放。在麻醉下进行手术半切后,大鼠表现出偏瘫的特征性体征,同侧后肢没有运动。 3天后,电子显微镜图像显示神经元细胞器和髓鞘的整体变性,但突触似乎是完整的。在离体实验中,脊髓损伤不影响摄取,但在静息时和响应轴突刺激时增加[3 H] NA释放。研究了选择性去甲肾上腺素再摄取抑制剂尼西西汀的作用,以确定NA释放增加的潜在机制。尼索西汀增强了刺激引起的[3H] NA从非损伤组织中的释放,但在损伤后逐渐消失,这取决于半切后所经过的时间(1天和3天),这表明末端的去甲肾上腺素转运蛋白结合位点变为分权后受损。

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