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DOI: 10.1055/s-2005-915206
Early Effect of Gene Therapy on a Direct Muscle Neurotization Model
Publikationsverlauf
Accepted: April 26, 2005
Publikationsdatum:
12. August 2005 (online)
ABSTRACT
Direct nerve-to-muscle neurotization has been the subject of both clinical and experimental studies. In this study, the authors report a new animal model to test the regenerative properties of a nerve (musculocutaneous) implanted in a muscle (biceps). They also report the early effects of the application at the implantation site of exogenously administered Brain Derived Nerve Factor (BDNF) and of endogenously produced BDNF, via the administration of an adenoviral construct with a tissue-specific promotor for muscle cells (AdRSV), and containing the BDNF gene. Evaluation included behavioral testing (grooming test), electrical stimulation, Western blot analysis of the distal implanted nerve to determine the presence of locally produced BDNF, and motor end-plate staining of the biceps muscle. At the early time point of 1 week following the musculocutaneous nerve to biceps muscle implantation, there was no increased production of recombinant BDNF at the distal implanted musculocutaneous nerve, as assessed by Western blot analysis. Therefore, there was no significant difference in the behavioral evaluation of the animals at 1 week; the Terzis grooming test showed no statistical difference among groups, but a trend toward better function for the BDNF and the high-dose AdRSV-BDNF groups, compared to the control groups. There was also no difference in the histologic appearance and number of the motor end-plates at the implantation site, compared to the controls. The electrical stimulation of the MC nerve did not produce statistically significant results among the experimental groups. In this direct nerve to muscle neurotization model, the application of AdRSV-BDNF at 3 × 109 pfu/ul did not show enhanced production of BDNF at 1 week.
KEYWORDS
Nerve-to-muscle neurotization - BDNF - adenoviral construct
REFERENCES
- 1 Heineke D. Die directe Enipflanzung des Nerven in den Muskel. Zentralb Chir. 1914; 41 465-466
- 2 Brunelli G A, Brunelli G R. Direct muscle neurotization. J Reconstr Microsurgery. 1993; 9 81-90
- 3 MacKinnon S, Hunter G. Neurotization of the rat soleus muscle. A quantitative analysis of reinnervation. J Hand Surg. 1993; 9 77-80
- 4 Terenghi G. Peripheral nerve regeneration and neurotrophic factors. J Anat. 1999; 14 1-14
- 5 Yin Q, Kemp J, Frostnick S. Neurotrophins, neurons and peripheral nerve regeneration. J Hand Surg. 1988; 23B 433-437
- 6 Kishino A, Ishige Y, Tatsuno T, Nakayamo C, Noguchi H. BDNF prevents and reverses adult motor neuron degeneration and induces axonal outgrowth. Exp Neurol. 1997; 144 273-286
- 7 Lewin S L, Utley D S, Cheng E T, Verity A N, Terris D J. 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
- 8 Sendter M, Dittrich F, Hughes R A, Thoenen H. Actions of CNTF and neurotrophins on degenerating motor neurons: preclinical studies and clinical implications. J Neurol Sci. 1994; 124 (Suppl) 77-83
- 9 Tonra J R, Curtis R, Wong V et al.. Axotomy upregulates the anterograde transport and expression of Brain-Derived Neurotrophic Factor by sensory neurons. J Neurosci. 1998; 18 4374-4383
- 10 Altar C A, DiStefano P S. Neurotrophin trafficking by anterograde transport. Trends Neurosci. 1998; 21 433-437
- 11 Reynolds A J, Hendry I A. A technique for 125I-labelling of neurotrophins and the use of retrograde axonal transport as a bioassay. Brain Res Brain Res Protoc. 1999; 3 308-312
- 12 Curtis R, Tonra J R, Stark J L et al.. Neuronal injury increases retrograde axonal transport of the neurotrophins to spinal sensory neurons and motor neurons via multiple receptor mechanisms. Mol Cell Neurosci. 1998; 12 105-118
- 13 Haase G, Pettman B, Vigne E, Castlenau-Ptakine L, Schmalbruch H, Kahn A. Adenovirus mediated transfer of neurotrophin-3 gene into skeletal muscle of pmn mice: therapeutic effects and mechanisms of action. J Neurol Sci. 1998; 160 suppl 1 S97-S105
- 14 Gimenez Y, Ribotta M, Revah F, Pradier L, Loquet I, Mallet J. Prevention of motor neuron death by adenovirus mediated neurotrophic factors. J Neurosci Res. 1997; 483 281-285
- 15 Baumgartner B J, Shine D H. Targeted transduction of CNS neurons with adenoviral vectors carrying neurotrophic factor genes confers neuroprotection that exceeds the transduced population. J Neurosci. 1997; 17 6504-6511
- 16 Rabinovsky E D, Papakonstantinou K, Nichols T, Shenaq S M. The peripheral nerve as a target for gene therapy. In: Proceedings of the Society for Neuroscience San Diego, California; November 11-16, 1995
- 17 Akli S, Caillud C, Vigne E et al.. Transfer of a foreign gene into the brain using adenoviral vectors. Nat Genet. 1993; 3 224-228
- 18 Inciong J, Marrocco W, Terzis J****k. Efficacy of intervention strategies in a brachial plexus global avulsion model in the rat. Plast Reconstr Surg. 2000; 105 2059-2071
- 19 Gorio A. Muscular reinnervation - II. Sprouting, synapse formation and repression. J Neurosci. 1983; 8 403-416
- 20 Brunelli G. Direct neurotization of severely damaged muscles. J Hand Surg. 1982; 7 572-579
- 21 Sakellarides H T, James L, Sorbie C. Reinnervation of denervated muscles by nerve transplantation. Clin Orthop. 1972; 83 194-201
- 22 Payne S H, Brushart T M. Neurotization of the rat soleus muscle: a quantitative analysis of reinnervation. J Hand Surg. 1997; 22A 640-643
- 23 Park D M, Shon S K, Kim Y J. Direct muscle neurotization in rat soleus muscle. J Reconstr Microsurg. 2000; 16 135-139
- 24 Papalia I, Lacroix C, Brunelli F, Stagno d' Alcontres F. Direct muscle neurotization after end-to-side neurorrhaphy. J Reconstr Microsurg. 2001; 17 237-246
- 25 Mousavi K, Parry D J, Jasmin B J. BDNF rescues myosin heavy chain IIB muscle fibers after neonatal nerve injury. Am J Physiol Cell Physiol. 2004; 287 C22-C29
- 26 Nakaizumi T, Kawamoto K, Minoda R, Raphael Y. Adenovirus-mediated expression of brain-derived neurotrophic factor protects spiral ganglion neurons from ototoxic damage. Audiol Neurootol. 2004; 9 135-143
Julia K TerzisM.D. Ph.D.
Microsurgery Research Center, EVMS
700 Olney Road, Lewis Hall, Room 2055
Norfolk, VA 23501