Neural Regeneration Research ›› 2017, Vol. 12 ›› Issue (4): 629-636.doi: 10.4103/1673-5374.205104

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Recombinant human fibroblast growth factor-2 promotes nerve regeneration and functional recovery after mental nerve crush injury

Sung Ho Lee1, Wei-Peng Jin1, Na Ri Seo1, Kang-Mi Pang1, Bongju Kim2, Soung-Min Kim1, Jong-Ho Lee1, 3   

  1. 1 Dental Research Institute, Department of Oral and Maxillofacial Surgery, Seoul National University School of Dentistry, Seoul, Korea; 2 Dental Life Science Research Institute, Clinical Translational Research Center for Dental Science, Seoul National University Dental Hospital, Seoul, Korea; 3 Dental Research Institute, Seoul National University, Seoul, Korea
  • Received:2017-03-17 Online:2017-04-15 Published:2017-04-15
  • Contact: Jong-Ho Lee, D.D.S., M.S.D., Ph.D., leejongh@snu.ac.kr.
  • Supported by:

    This study was supported by a grant from the Korea Healthcare Technology R&D Project, Ministry for Health, Welfare & Family Affairs,
    Republic of Korea, No. A101578.

Abstract:

Several studies have shown that fibroblast growth factor-2 (FGF2) can directly affect axon regeneration after peripheral nerve damage. In this study, we performed sensory tests and histological analyses to study the effect of recombinant human FGF-2 (rhFGF2) treatment on damaged mental nerves. The mental nerves of 6-week-old male Sprague-Dawley rats were crush-injured for 1 minute and then treated with 10 or 50 μg/mL rhFGF2 or PBS in crush injury area with a mini Osmotic pump. Sensory test using von Frey filaments at 1 week revealed the presence of sensory degeneration based on decreased gap score and increased difference score. However, at 2 weeks, the gap score and difference score were significantly rebounded in the mental nerve crush group treated with 10 μg/mL rhFGF2. Interestingly, treatment with 10 μg/mL rhFGF had a more obviously positive effect on the gap score than treatment with 50 μg/mL rhFGF2. In addition, retrograde neuronal tracing with Dil revealed a significant increase in nerve regeneration in the trigeminal ganglion at 2 and 4 weeks in the rhFGF2 groups (10 μg/mL and 50 μg/mL) than in the PBS group. The 10 μg/mL rhFGF2 group also showed an obviously robust regeneration in axon density in the mental nerve at 4 weeks. Our results demonstrate that 10 μg/mL rhFGF induces mental nerve regeneration and sensory recovery after mental nerve crush injury.

Key words: nerve regeneration, mental nerve, fibroblast growth factor, crush injury, sensory neuron, functional recovery, neural regeneration