Gonçalves Leonor, Almeida Armando, Pertovaara Antti
Biomedicum Helsinki, Biomedicine/Physiology, POB 63, 00014 University of Helsinki, Finland.
Eur J Neurosci. 2007 Oct;26(8):2188-95. doi: 10.1111/j.1460-9568.2007.05832.x. Epub 2007 Sep 24.
The spared nerve injury (SNI) model of peripheral neuropathy produces a robust and long-lasting hypersensitivity. Previous behavioural studies suggest that brainstem-spinal pathways originating in or relaying through the rostroventromedial medulla (RVM) contribute to neuropathic hypersensitivity. We determined whether SNI induces changes in response properties of RVM neurons that might influence descending modulation of nociception. RVM neurons included in the study were classified into presumably pronociceptive ON-cells and antinociceptive OFF-cells (giving excitatory or inhibitory responses to noxious stimulation, respectively). Spontaneous activity and the response to cold, pinch and colorectal distension were assessed under light anaesthesia in the rat, 1 week and 8 weeks following nerve injury or sham operation. Spontaneous activity was increased 1 week but not 8 weeks after nerve injury in ON-cells but decreased in OFF-cells at both time points. In the SNI group, cold-evoked responses were enhanced particularly in ON-cells, independent of the postoperative time point. Responses of ON-cells to pinch and visceral stimulation were enhanced 8 weeks but not 1 week following nerve injury, whereas OFF-cell responses to pinch or colorectal distension were not changed. The results indicate that SNI induces pronociceptive changes in spontaneous activities of ON-cells and OFF-cells and peripherally evoked responses of ON-cells that vary with the postoperative time point. Increased ON-cell activity and decreased OFF-cell activity in the RVM are likely to enhance spinal nociception in a tonic fashion, whereas increased responses of ON-cells to peripheral stimulation are likely to enhance ascending nociceptive signals by a positive feedback following peripheral noxious stimulation.
周围神经病变的 spared 神经损伤(SNI)模型会产生强烈且持久的超敏反应。先前的行为学研究表明,起源于延髓头端腹内侧区(RVM)或经其中继的脑干 - 脊髓通路会导致神经病理性超敏反应。我们确定 SNI 是否会诱导 RVM 神经元反应特性的变化,而这些变化可能会影响伤害性感受的下行调制。本研究纳入的 RVM 神经元被分为可能具有促伤害性的 ON 细胞和抗伤害性的 OFF 细胞(分别对有害刺激产生兴奋性或抑制性反应)。在大鼠接受神经损伤或假手术后 1 周和 8 周,于轻度麻醉下评估其自发活动以及对冷刺激、夹捏和结肠扩张的反应。神经损伤后 1 周,ON 细胞的自发活动增加,但 8 周时未增加;而在两个时间点,OFF 细胞的自发活动均减少。在 SNI 组中,冷诱发反应尤其在 ON 细胞中增强,且与术后时间点无关。神经损伤后 8 周而非 1 周,ON 细胞对夹捏和内脏刺激的反应增强,而 OFF 细胞对夹捏或结肠扩张的反应未改变。结果表明,SNI 会诱导 ON 细胞和 OFF 细胞自发活动以及 ON 细胞外周诱发反应出现促伤害性变化,且这些变化随术后时间点而不同。RVM 中 ON 细胞活动增加和 OFF 细胞活动减少可能会以紧张性方式增强脊髓伤害性感受,而 ON 细胞对外周刺激反应的增加可能会通过外周有害刺激后的正反馈增强上行伤害性信号。