Restoring vocal fold movement after transection and immediate suturing of the recurrent laryngeal nerve with local application of basic fibroblast growth factor: An experimental study in the rat

Laryngoscope

Volumn 114, Issue 7, 2004, Pages 1247-1252

  Motoyoshi, Kazumi ^a   Hyodo, Masamitsu ^a   Yamagata, Takahiko ^a   Gyo, Kiyofumi ^a  

^a EHIME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Basic fibroblast growth factor; Laryngeal muscle; Osmotic pump; Recurrent laryngeal nerve; Vocal fold movement

Indexed keywords

BASIC FIBROBLAST GROWTH FACTOR; PHOSPHATE;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; HISTOPATHOLOGY; IMAGE ANALYSIS; LARYNGEAL NERVE; LARYNX CARTILAGE; MALE; MUSCLE CELL; NERVE TRANSECTION; NONHUMAN; OSMOTIC PUMP; POSTOPERATIVE PERIOD; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RAT; SUTURE; TREATMENT OUTCOME; VIDEORECORDER; VOCAL CORD;

ANIMALS; FIBROBLAST GROWTH FACTORS; MALE; NECK MUSCLES; NERVE REGENERATION; RATS; RATS, WISTAR; RECURRENT LARYNGEAL NERVE; VOCAL CORD PARALYSIS; VOCAL CORDS;

EID: 3242664532     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-200407000-00020     Document Type: Article

References (30)

1. Komori M. Effects of neurotrophic factors on regeneration of denervated recurrent laryngeal nerve in the rat. Pract Otol (Kyoto) 1999;92:677-686.
2. Unsicker K, Grothe C, Ludecke G, et al. Fibroblast growth factors: their roles in the central and peripheral nervous system. In: Loughlin SE, Fallon JH, eds. Neurotrophic Factors. New York: Academic Press, 1993:313-338.
3. Anderson KJ, Dam D, Lee S, Cotman CW. Basic fibroblast growth factor prevents death of lesioned cholinergic neurons in vivo. Nature 1988;332:360-361.
4. Otto D, Unsicker K, Grothe C. Pharmacological effects of nerve growth factor and fibroblast growth factor applied to the transsectioned sciatic nerve on neuron death in adult rat dorsal root ganglia. Neurosci Lett 1987;83:156-160.
5. Danielsen N, Pettmann B, Vahlsing HL, et al. Fibroblast growth factor effect's on peripheral nerve generation in a silicone chamber model. J Neurosci Res 1988;20:320-330.
6. Gerney ME, Yamamoto H, Korn Y. Induction of motor neuron sprouting in vivo by ciliary neurotrophic factor and basic fibroblast growth factor. J Neurosci 1992;12:3241-3247.
7. Shin T. Regeneration of recurrent laryngeal nerve after injury. Otologica (Fukuoka) 1971;17:117-121.
8. Mu LC, Yang SL. Electromyographic study on end-to-end anastomosis of the recurrent laryngeal nerve in dogs. Laryngoscope 1990;100:1009-1017.
9. Nahm I, Shin T, Watanabe H, Maeyama T. Misdirection of injured recurrent laryngeal nerve in the cat. Am J Otolaryngol 1993;14:43-48.
10. Siribodhi C, Sundmaker W, Atkins JP, Bonner FJ. Electromyographic studies of laryngeal paralysis and regeneration of laryngeal motor nerves in dogs. Laryngoscope 1963;73:148-164.
11. Hiroto I, Hirano M, Tomita H. Electromyographic investigations of human vocal paralysis. Ann Otol Rhinol Laryngol 1968;77:296-304.
12. Tashiro T. Experimental studies on the reinnervation of larynx after accurate neurorrhaphy. Laryngoscope 1972;82:225-236.
13. Gordon JH, McCabe BF. The effect of accurate neurorrhaphy on reinnervation and return of laryngeal function. Laryngoscope 1968;78:236-250.
14. Gacek R, Malmgren LT, Lyon MJ. Localization of adductor and abductor motor nerve fibers to the larynx. Ann Otol Rhinol Laryngol 1977;86:770-776.
15. Boles R, Fritzell B. Injury and repair of the recurrent laryngeal nerve in dogs. Laryngoscope 1969;79:1405-1418.
16. Tomita H. An electromyographic study of recurrent laryngeal nerve paralysis. J Otolaryngol Jpn 1967;70:963-985.
17. Dedo HH. Electromyographic and visual evaluation of recurrent laryngeal nerve anastomosis in dogs. Ann Otol Rhinol Laryngol 1971;80:664-668.
18. Shiotani A, Flint PW. Modulation of myosin heavy chains in rat laryngeal muscles after denervation. Laryngoscope 2001;111:472-477.
19. Fujimoto E, Mizoguchi A, Hanada K, et al. Basic fibroblast growth factor promotes extension of regenerating axons of peripheral nerve: in vivo experiments using a Schwann cell basal lamina tube model. J Neurocytol 1997;26:511-528.
20. Sunderland SS. Regeneration of the axon and associated changes. In: Sunderland SS, ed. Nerves and Nerve Injuries. New York: Churchill Livingstone, 1978:108-132.
21. Newman JP, Verity AN, Hawatmeh S, et al. Ciliary neurotrophic factor enhances peripheral nerve regeneration. Arch Otolaryngol Head Neck Surg 1996;122:399-403.
22. Lewin SL, Utley DS, Cheng ET, et al. Simultaneous treatment with BDNF and CNTF after peripheral nerve transection and repair enhances rate of functional recovery compared with BDNF treatment alone. Laryngoscope 1997;107:992-999.
23. Grothe C, Wewetzer K, Langrenge A, Unsicker K. Effect of basic fibroblast growth factor on survival and choline acetyltransferase development of spinal cord neurons. Dev Brain Res 1991;62:257-261.
24. Ide C, Tohyama K, Tajima K, et al. Long acellular nerve transplants for allogeneic grafting and the effects of basic fibroblast growth factor on the growth of regenerating axons in dogs. Exp Neurol 1998;154:99-112.
25. Edelman ER, Mathiowitz E, Langer R, Klagsbrum M. Controlled and modulated release of basic fibroblast growth factor. Bio Mat 1991;12:619-626.
26. Iizuka T. Experimental studies on the nerve interception and atrophy of the intrinsic muscles of the larynx. J Otolaryngol Jpn 1965;69:176-195.
27. Helgren ME, Squinto SP, Davis HL, et al. Trophic effect of ciliary neurotrophic factor on denervated skeletal muscle. Cell 1994;76:493-504.
28. Anderson JE, Liu L, Kardami E. Distinctive patterns of basic fibroblast growth factor (bFGF) distribution in degenerating and regenerating areas of dystrophic (mdx) striated muscles. Dev Biol 1991;147:96-107.
29. Guthridge M, Wilson M, Cowling J, et al. The role of basic fibroblast growth factor in skeletal muscle regeneration. Growth Factors 1992;6:53-63.
30. Lefaucheur JP, Sëbille A. Muscle regeneration following injury can be modified in vivo by immune neutralization of basic fibroblast growth factor, transforming growth factor β1 or insulin-like growth factor I. J Neuroimmunol 1995;57:85-91.