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Effects of neutralizing antibodies to tumor necrosis factor-alpha on nucleus pulposus-induced abnormal nociresponses in rat dorsal horn neurons.

机译:抗肿瘤坏死因子-α的中和抗体对大鼠背角神经元髓核诱导的异常Nociresponses的影响。

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STUDY DESIGN: The effect of an anti-tumor necrosis factor alpha (anti-TNFalpha) antibody on abnormal discharges caused by application of nucleus pulposus to the nerve root was investigated in an electrophysiologic study. OBJECTIVES: To assess whether inhibition of TNFalpha can reduce nucleus pulposus-induced abnormal discharges. SUMMARY OF BACKGROUND DATA: It has been shown that TNFalpha, a proinflammatory cytokine, is a key pathogenic factor in the development of nucleus pulposus-induced abnormal discharges as a pain sensation. However, the electrophysiologic mechanisms involved in sciatica after disc herniation still have not been elucidated. METHODS: Extracellular activities of wide-dynamic-range neurons were assessed in 21 rats. Autologous nucleus pulposus harvested from the tail was applied to the L5 nerve root. The animals were simultaneously treated with antibodies to TNFalpha (anti-TNF + nucleus pulposus group) and with phosphate-buffered saline (nucleus pulposus group). As a control (control group), a similar volume of muscle was applied to the nerve root with phosphate-buffered saline. Responses of wide-dynamic-range neurons to noxious and innocuous stimuli were examined for 2 hours. RESULTS: Discharges evoked during noxious stimulation and discharges after withdrawal of stimulation in the nucleus pulposus group were significantly higher than those in the control group (P < 0.05). In the anti-TNF + nucleus pulposus group, discharges after withdrawal of stimulation were remarkably inhibited, as compared with those of the nucleus pulposus group (P < 0.05). However, evoked discharges during stimulation apparently were not inhibited. Responses to innocuous stimulation did not change throughout the measurements. CONCLUSIONS: These data indicate that application of TNFalpha antibodies to the nerve root partially prevents the nucleus pulposus-induced abnormal nociresponses. Therefore, anti-TNFalpha treatment may have a therapeutic effect on sciatica after lumbar disc herniation.
机译:研究设计:在电生理研究中,研究了抗肿瘤坏死因子α(anti-TNFalpha)抗体对髓核施加于神经根引起的异常放电的影响。目的:评估TNFα的抑制作用是否可以减少髓核引起的异常放电。背景数据概述:已经显示,TNFα(一种促炎细胞因子)是髓核引起的异常放电(作为一种疼痛感)的发展中的关键致病因素。但是,仍未阐明椎间盘突出症后坐骨神经痛的电生理机制。方法:在21只大鼠中评估了宽动态范围神经元的细胞外活性。从尾巴收获的自体髓核应用于L5神经根。同时用抗TNFα的抗体(抗TNF +髓核组)和磷酸盐缓冲液(髓核组)治疗动物。作为对照组(对照组),用磷酸盐缓冲盐水将类似体积的肌肉施加于神经根。检查了2个小时的宽动态范围神经元对有害和无害刺激的反应。结果:髓核组在有毒刺激过程中引起的放电和停止刺激后的放电显着高于对照组(P <0.05)。与髓核组相比,抗TNF +髓核组显着抑制刺激后的放电(P <0.05)。然而,刺激期间诱发的放电显然没有被抑制。在整个测量过程中,对无害刺激的反应均未改变。结论:这些数据表明在神经根上应用TNFα抗体可部分预防髓核诱导的异常Nociresponses。因此,抗TNFα治疗可能对腰椎间盘突出症后的坐骨神经痛有治疗作用。

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