Neuroscience Research Institute and Department of Physiology, Korea University College of Medicine, 126-1 Anam-dong 5 Ga, Sungbuk-Gu, Seoul 136-705, Republic of Korea.
Eur J Pain. 2011 May;15(5):459-66. doi: 10.1016/j.ejpain.2010.09.014. Epub 2010 Oct 20.
The vast majority of human peripheral nerve injuries occur in the upper limb, whereas the most animal studies have been conducted using the hindlimb models of neuropathic pain, involving damages of the sciatic or lumbar spinal nerve(s). We attempted to develop a rat forelimb model of peripheral neuropathy by partial injury of the median and ulnar nerves. The halves of each nerve were transected by microscissors at about 5mm proximal from the elbow joint and behavioral signs of neuropathic pain, such as mechanical and cold allodynia, and heat hyperalgesia, were monitored up to 126 days following nerve injury. Mechanical allodynia was assessed by measuring the forepaw withdrawal threshold to von Frey filaments, and cold allodynia was evaluated by measuring the time spent in lifting or licking the forepaw after applying acetone to it. Heat hyperalgesia was also monitored by investigating the forepaw withdrawal latencies using the Hargreaves' test. After the nerve injury, the experimental animals exhibited long-lasting clear neuropathic pain-like behaviors, such as reduced forepaw withdrawal threshold to von Frey filaments, the increased response duration of the forepaw to acetone application, and the decreased withdrawal latency to radiant heat stimulation. These behaviors were significantly alleviated by administration of gabapentin (5 or 50mg/kg, i.p.) in a dose-dependent manner. Therefore, these abnormal sensitivities are interpreted as the signs of neuropathic pain following injury of the median and ulnar nerves. Our rat forelimb model of neuropathic pain may be useful for studying human neuropathic pain and screening for valuable drug candidates.
绝大多数人类周围神经损伤发生在上肢,而大多数动物研究使用的是后肢神经性疼痛模型,涉及坐骨或腰椎脊神经的损伤。我们试图通过部分损伤正中神经和尺神经来建立大鼠前肢周围神经病变模型。用显微剪刀在距肘关节约 5mm 处将每条神经的两半切断,并在神经损伤后 126 天内监测神经性疼痛的行为迹象,如机械性和冷感觉异常痛以及热痛觉过敏。机械性感觉异常痛通过测量 von Frey 纤维引起的前爪回缩阈值来评估,冷感觉异常痛通过测量施加丙酮后前爪抬起或舔舐的时间来评估。还通过使用 Hargreaves 试验研究前爪回缩潜伏期来监测热痛觉过敏。神经损伤后,实验动物表现出持久的明显神经性疼痛样行为,例如 von Frey 纤维引起的前爪回缩阈值降低、前爪对丙酮应用的反应持续时间延长以及对辐射热刺激的回缩潜伏期缩短。这些行为通过给予加巴喷丁(5 或 50mg/kg,ip)以剂量依赖性方式显著缓解。因此,这些异常敏感性被解释为正中神经和尺神经损伤后的神经性疼痛迹象。我们的大鼠前肢神经性疼痛模型可能有助于研究人类神经性疼痛和筛选有价值的候选药物。