Volume 15, Issue 5 pp. 459-466

A novel rat forelimb model of neuropathic pain produced by partial injury of the median and ulnar nerves

Hanju Yi

Hanju Yi

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

These authors equally contributed to this study.

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Myung Ah Kim

Myung Ah Kim

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

These authors equally contributed to this study.

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Seung Keun Back

Seung Keun Back

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

These authors equally contributed to this study.

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Jong Shin Eun

Jong Shin Eun

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

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Heung Sik Na

Corresponding Author

Heung Sik Na

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

Department of Physiology, Korea University College of Medicine, 126-1, Anam-dong 5 Ga, Seongbuk-Ku, Seoul 136–705, Republic of Korea. Tel.: +82 2 920 6188; fax: +82 2 925 5492 [email protected].Search for more papers by this author
First published: 13 January 2012
Citations: 10

Abstract

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 5 mm 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 50 mg/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.

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