Department of Physical Therapy, Faculty of Rehabilitation, Niigata University of Health and Welfare, Niigata 950-3198, Japan.
Department of Applied Pharmacology, Faculty of Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.
Neurosci Res. 2022 Aug;181:87-94. doi: 10.1016/j.neures.2022.03.005. Epub 2022 Mar 16.
The pathological mechanisms of fibromyalgia (FM) are largely unknown. Recently, a rat reserpine-induced pain model showing exaggerated pain-related behaviors to mechanical and thermal stimuli has been used in FM research. However, the model has not been fully characterized. Here, we investigated nociceptive hypersensitivity to chemical stimuli and its spinal mechanisms to further characterize the model. The rat model was induced by administering reserpine to the nervous system. Nociceptive behaviors to chemical stimuli were quantified using the formalin pain test, and neuronal activation of the stimuli was examined using spinal c-Fos immunohistochemistry and electrophysiological recordings of superficial dorsal horn (SDH) neurons. The duration of pain-related behaviors was prolonged in both phases I (0-5 min) and II (10-60 min) and the interphase; and the number of c-Fos-immunoreactive nuclei increased in laminae I-II, III-IV, and V-VI at the spinal segments L3-L5 on the side ipsilateral to the formalin injection, and these factors were significantly and positively correlated. The action potentials of SDH neurons induced by formalin injection were markedly increased in rats treated with reserpine. These results demonstrate that pain-related behaviors are facilitated by noxious chemical stimuli in a rat reserpine-induced FM model, and that the behavioral hypersensitivity is associated with hyperactivation of SDH neurons.
纤维肌痛(FM)的病理机制在很大程度上尚不清楚。最近,一种大鼠利血平诱导的疼痛模型已被用于 FM 研究,该模型表现出对机械和热刺激的过度疼痛相关行为。然而,该模型尚未得到充分表征。在这里,我们研究了对化学刺激的痛觉过敏及其脊髓机制,以进一步表征该模型。通过向神经系统给予利血平来诱导大鼠模型。使用福马林疼痛测试来量化化学刺激引起的痛觉过敏行为,并使用脊髓 c-Fos 免疫组织化学和浅层背角(SDH)神经元的电生理记录来检测刺激的神经元激活。在 I 期(0-5 分钟)和 II 期(10-60 分钟)以及相间,与福尔马林注射侧的 L3-L5 脊髓节段的 I-II、III-IV 和 V-VI 层中,疼痛相关行为的持续时间延长,并且 c-Fos 免疫反应性核的数量增加,这些因素呈显著正相关。在接受利血平治疗的大鼠中,福尔马林注射诱导的 SDH 神经元的动作电位明显增加。这些结果表明,在大鼠利血平诱导的 FM 模型中,有害化学刺激促进了与疼痛相关的行为,并且行为敏感性与 SDH 神经元的过度激活有关。