Yokoyama Takeshi, Maeda Yumi, Audette Katherine M, Sluka Kathleen A
Graduate Program in Physical Therapy and Rehabilitation Science, The University of Iowa, Iowa City, Iowa 52242-1190, USA.
J Pain. 2007 May;8(5):422-9. doi: 10.1016/j.jpain.2006.11.007. Epub 2007 Feb 9.
Pregabalin is used for treatment of neuropathic pain conditions. The present study evaluated effects of pregabalin in 2 rat models of muscle-induced hyperalgesia: Inflammatory and noninflammatory. Muscle hyperalgesia (withdrawal threshold to compression of the muscle) and cutaneous hyperalgesia of the paw (withdrawal threshold to von Frey filaments) were measured before and after induction of hyperalgesia and after treatment with pregabalin (saline, 10 to 100 mg/kg i.p.). In the inflammatory model, 3% carrageenan injected into 1 gastrocnemius muscle decreased the mechanical withdrawal threshold of the paw bilaterally and the compression withdrawal threshold of the muscle ipsilaterally 2 weeks later. Pregabalin (10 to 100 mg/kg) increased the compression withdrawal threshold of the inflamed muscle when compared with vehicle controls. Pregabalin also increased the mechanical withdrawal threshold of the paw bilaterally, but only with 100 mg/kg. In the noninflammatory model, 2 unilateral injections of acidic saline into the gastrocnemius muscle produced bilateral cutaneous and muscle hyperalgesia 24 hours after the second injection. Pregabalin (10 to 100 mg/kg i.p.) significantly increased the compression withdrawal thresholds of the muscle and the mechanical withdrawal threshold of the paw bilaterally when compared with vehicle. However, pregabalin also has significant motor effects at the higher doses (60 to 100 mg/kg). Therefore, pregabalin reduces both muscle and cutaneous hyperalgesia that occurs after muscle insult in 2 animal models of muscle pain at doses that do not produce ataxia.
This study shows that pregabalin reduces both cutaneous and muscle hyperalgesia in inflammatory and noninflammatory models of muscle pain. Thus, pregabalin may be an effective treatment for people with chronic muscle pain.
普瑞巴林用于治疗神经性疼痛。本研究评估了普瑞巴林在两种肌肉诱导性痛觉过敏大鼠模型中的作用:炎症性和非炎症性。在诱导痛觉过敏之前和之后以及用普瑞巴林(生理盐水、10至100毫克/千克腹腔注射)治疗之后,测量肌肉痛觉过敏(肌肉受压的撤针阈值)和爪部皮肤痛觉过敏(对von Frey细丝的撤针阈值)。在炎症模型中,向一侧腓肠肌注射3%角叉菜胶会使双侧爪部的机械撤针阈值以及两周后同侧肌肉的压迫撤针阈值降低。与溶剂对照组相比,普瑞巴林(10至100毫克/千克)可提高炎症肌肉的压迫撤针阈值。普瑞巴林还可使双侧爪部的机械撤针阈值升高,但仅在剂量为100毫克/千克时。在非炎症模型中,向腓肠肌单侧注射两次酸性生理盐水会在第二次注射后24小时产生双侧皮肤和肌肉痛觉过敏。与溶剂相比,普瑞巴林(10至100毫克/千克腹腔注射)可显著提高双侧肌肉的压迫撤针阈值和爪部的机械撤针阈值。然而,普瑞巴林在较高剂量(60至100毫克/千克)时也有显著的运动效应。因此,普瑞巴林可减轻两种肌肉疼痛动物模型中肌肉损伤后出现的肌肉和皮肤痛觉过敏,且所用剂量不会导致共济失调。
本研究表明,普瑞巴林可减轻炎症性和非炎症性肌肉疼痛模型中的皮肤和肌肉痛觉过敏。因此,普瑞巴林可能是慢性肌肉疼痛患者的一种有效治疗方法。