School of Medicine, College of Medicine, Fu Jen Catholic University, Taipei, Taiwan.
Anesthesiology. 2012 Feb;116(2):415-31. doi: 10.1097/ALN.0b013e318242a801.
Neuroprotective effects of hypothermia on peripheral nerve injury remain uncertain. This study investigated the efficacy of hypothermia in attenuating neuropathic pain and glial activation in the cuneate nucleus in a median nerve chronic constriction injury (CCI) model.
Sprague-Dawley rats (n = 246) that underwent median nerve ligature at the elbow received various degrees of regional and whole-body hypothermia 15 min before CCI and 5 h, 1, 3, and 5 days after CCI. Hypothermia was maintained for 4 h. Seven days after CCI, behavioral and electrophysiological testings were conducted. Immunohistochemistry, immunoblotting, and enzyme-linked immunosorbent assay were used for qualitative and quantitative analysis of glial activation and measuring pro-inflammatory cytokines, respectively.
Mild (32°C) and deep (28°C) regional hypothermia administered preinjury and 5 h postinjury attenuated neuropathic pain and glial activation. Application of whole-body hypothermia preinjury and 5 h postinjury provided a similar therapeutic effect. However, whole-body hypothermia, but not regional hypothermia, applied 1, 3, and 5 days postinjury attenuated glial activation and neuropathic pain. Similarly, on days 1, 3, and 5 postinjury, only whole-body hypothermia was effective in decreasing proinflammatory cytokine levels. The increase in injury discharge observed after CCI could be suppressed by regional or whole-body hypothermia at different stages of nerve injury.
At the early stage following nerve injury, regional and whole-body hypothermia suppresses ectopic discharges, and consequently inhibits glial activation and neuropathic pain. At the later stage, pain processing is mediated mainly by cytokines released from activated microglia; therefore, only whole-body hypothermia is effective in modulating pain.
低温对周围神经损伤的神经保护作用仍不确定。本研究探讨了低温在减轻正中神经慢性缩窄性损伤(CCI)模型中楔状核神经病理性疼痛和神经胶质激活中的疗效。
肘正中神经结扎的 Sprague-Dawley 大鼠(n=246)在 CCI 前 15 分钟和 CCI 后 5 小时、1 天、3 天和 5 天接受不同程度的局部和全身低温治疗。低温持续 4 小时。CCI 后 7 天进行行为和电生理测试。免疫组织化学、免疫印迹和酶联免疫吸附试验分别用于定性和定量分析神经胶质激活和测量促炎细胞因子。
轻度(32°C)和深度(28°C)局部低温在损伤前和损伤后 5 小时应用可减轻神经病理性疼痛和神经胶质激活。全身低温在损伤前和损伤后 5 小时应用提供了类似的治疗效果。然而,全身低温而非局部低温在损伤后 1、3 和 5 天应用可减轻神经胶质激活和神经病理性疼痛。同样,在损伤后 1、3 和 5 天,只有全身低温可有效降低促炎细胞因子水平。CCI 后观察到的损伤放电增加可通过不同阶段的神经损伤时的局部或全身低温来抑制。
在神经损伤的早期,局部和全身低温抑制异位放电,从而抑制神经胶质激活和神经病理性疼痛。在后期,疼痛处理主要由激活的小胶质细胞释放的细胞因子介导;因此,只有全身低温可有效调节疼痛。