Vance Carol G T, Radhakrishnan Rajan, Skyba David A, Sluka Kathleen A
Graduate Program in Physical Therapy and Rehabilitation Science, University of Iowa, Iowa City, IA 52242, USA.
Phys Ther. 2007 Jan;87(1):44-51. doi: 10.2522/ptj.20060032. Epub 2006 Dec 1.
Clinical studies of transcutaneous electrical nerve stimulation (TENS) have used a variety of outcome measures to assess its effectiveness, with conflicting results. It is possible that TENS is effective on some measures of pain and not on others. The purpose of this study was to test the hypothesis that TENS reduces primary hyperalgesia of the knee induced by joint inflammation.
Male Sprague-Dawley rats were used in this study.
Inflammation of the knee joint was induced by intra-articular injection of a mixture of 3% kaolin and 3% carrageenan. Primary hyperalgesia was measured as the compression withdrawal threshold of the knee joint before and after the induction of inflammation (4 hours, 24 hours, and 2 weeks) and after sham TENS treatment, treatment with high-frequency TENS (100 Hz), or treatment with low-frequency TENS (4 Hz).
The compression withdrawal threshold was significantly reduced at 4 hours, 24 hours, and 2 weeks after the induction of inflammation. Either high-frequency TENS or low-frequency TENS completely reversed the compression withdrawal threshold when applied at 24 hours or 2 weeks after the induction of inflammation but not when applied at 4 hours after the induction of inflammation.
These data suggest that TENS inhibits primary hyperalgesia associated with inflammation in a time-dependent manner after inflammation has already developed during both acute and chronic stages.
经皮电刺激神经疗法(TENS)的临床研究采用了多种结果指标来评估其有效性,结果相互矛盾。TENS可能对某些疼痛指标有效,而对其他指标无效。本研究的目的是检验TENS可减轻关节炎症引起的膝关节原发性痛觉过敏这一假设。
本研究使用雄性Sprague-Dawley大鼠。
通过关节内注射3%高岭土和3%角叉菜胶的混合物诱导膝关节炎症。原发性痛觉过敏通过在炎症诱导前、炎症诱导后(4小时、24小时和2周)以及假TENS治疗、高频TENS(100Hz)治疗或低频TENS(4Hz)治疗后测量膝关节的压迫撤离阈值来评估。
炎症诱导后4小时、24小时和2周时,压迫撤离阈值显著降低。在炎症诱导后24小时或2周时应用高频TENS或低频TENS均可完全逆转压迫撤离阈值,但在炎症诱导后4小时应用则无效。
这些数据表明,在炎症的急性和慢性阶段已经发展之后,TENS以时间依赖性方式抑制与炎症相关的原发性痛觉过敏。