Department of Rehabilitation, Nagasaki University Hospital, Nagasaki, Japan.
Department of Physical Therapy Science, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Pain Res Manag. 2021 Aug 6;2021:5592992. doi: 10.1155/2021/5592992. eCollection 2021.
Voluntary exercise is sufficient to protect against neuropathic pain. However, it is unclear whether voluntary exercise reduces immobilization-induced hyperalgesia. We examined the effect of voluntary forelimb exercise on immobilized-induced hyperalgesia in hind paws of rats. Wistar rats were randomly divided into the (1) both hind limbs immobilized group (IM group), (2) immobilization and exercise with nonimmobilized fore limbs group (EX group), and (3) control group. In the IM and EX groups, the bilateral ankle joints of each rat were immobilized in full plantar flexion with a plaster cast for eight weeks. In the EX group, voluntary exercise using nonimmobilized forelimbs in the running wheel was administered during the immobilization period, while hind limbs were kept immobilized (60 min/day, 5 days/week). Mechanical hyperalgesia in the hind paw was measured using a digital von Frey device every week. To investigate the abnormality of primary sensory neurons and central sensitization, the number of calcitonin gene-related peptide-positive cells in the dorsal root ganglion and the expression level of calcitonin gene-related peptide in the spinal dorsal horn were analyzed by immunohistochemical staining. Immobilization-induced mechanical hyperalgesia was inhibited in the EX group compared to the IM group at three weeks after immobilization. In the EX group, the number of calcitonin gene-related peptide-positive cells in the dorsal root ganglion and the expression level of calcitonin gene-related peptide were significantly decreased compared to those in the IM group. Our results therefore suggest that voluntary forelimb exercise during hind limb immobilization partially reduces immobilization-induced hyperalgesia by suppressing that the plastic changes of the primary sensory nerves that excessively transmit pain and increased responsiveness of nociceptive neurons in the spinal dorsal horn.
自愿运动足以预防神经性疼痛。然而,目前尚不清楚自愿运动是否会减轻固定引起的痛觉过敏。我们研究了自由前肢运动对大鼠后爪固定引起的痛觉过敏的影响。Wistar 大鼠随机分为以下三组:(1)双侧后肢固定组(IM 组),(2)固定并使用未固定前肢运动组(EX 组),和(3)对照组。在 IM 和 EX 组中,通过石膏绷带将每个大鼠的双侧踝关节固定在完全跖屈位,持续 8 周。在 EX 组中,在固定期间使用非固定前肢的跑步轮进行自愿运动,同时保持后肢固定(每天 60 分钟,每周 5 天)。每周使用数字 von Frey 设备测量后爪的机械性痛觉过敏。为了研究初级感觉神经元和中枢敏化的异常,通过免疫组织化学染色分析背根神经节中降钙素基因相关肽阳性细胞的数量和脊髓背角中降钙素基因相关肽的表达水平。与 IM 组相比,固定 3 周后 EX 组的固定诱导性机械性痛觉过敏受到抑制。与 IM 组相比,EX 组背根神经节中降钙素基因相关肽阳性细胞的数量和降钙素基因相关肽的表达水平均显著降低。因此,我们的研究结果表明,在下肢固定期间进行自由前肢运动可部分减轻固定引起的痛觉过敏,其机制可能是抑制过度传递疼痛的初级感觉神经的可塑性变化以及脊髓背角伤害感受神经元的反应性增加。