Phototherapy promotes regeneration and functional recovery of injured peripheral nerve

REFERENCES

• Strauch B. Use of nerve conduits in peripheral nerve repair. Hand Clinics 2000; 16: 123–130
   PubMed Web of Science ®Google Scholar
• Meek MF, Coed WI. Clinical use of nerve conduits in peripheral-nerve repair: review of the literature. Reconstr Microsurg 2002; 18: 97–109
   PubMed Web of Science ®Google Scholar
• Dvali L, Mackinnon S. Nerve repair, grafting, and nerve transfers. Clin Plast Surg 2003; 30: 203-221
   Google Scholar
• Lundborg G. Enhancing posttraumatic nerve regeneration. Peripher Nerv Syst 2002; 7: 139–140
   PubMed Web of Science ®Google Scholar
• Evans GR. Challenges to nerve regeneration. Semin Surg Oncol 2000; 19:312–318
   PubMed Web of Science ®Google Scholar
• Udina E, Ceballos D, Verdu E, Gold BG, Navarro X. Bimodal dose-dependence of FK506 on the rate of axonal regeneration in mouse peripheral nerve. Muscle Nerve 2002; 26: 348–355
   PubMed Web of Science ®Google Scholar
• Gudemez E, Ozer K, Cunningham B, Siemionow K, Browne E, Siemionow M. Dehydroepiandrosterone as an enhancer of functional recovery following crush injury to rat sciatic nerve. Microsurgery 2002; 22: 234-241
   Google Scholar
• Sarikcioglu L, Oguz N. Exercise training and axonal regeneration after sciatic nerve injury. Intl Neurosci 2001; 109:173–177
   PubMed Web of Science ®Google Scholar
• Lazar DA, Curra FP, Mohr B, McNutt LD, Kliot M, Mourad PD. Acceleration of recovery after injury to the peripheral nervous system using ultrasound and other therapeutic modalities. Neuro-surg Clin N Am 2001; 12: 353–357
   PubMed Web of Science ®Google Scholar
• Anders JJ, Borke RC, Woolery S. Low energy laser irradiation alters immunofluorescence of choline acetyltransferase (ChAT) in regenerating rat facial neurons. Neurosci 1991; 17: 1483
   Google Scholar
• Mulligan K, Woolery S, Anders JJ. The effect of low energy He-Ne laser irradiation on neurite elongation in vitro. Laser Surg Med Suppl 1991;3: 10
   Google Scholar
• Mester AF, Snow JB. Photochemical effects of low-intensity laser irradiation on wound healing and on the maturation adn regenera-tion of olfactory n euroep ithelia I explants. J Clin Laser Med Surg 1990; 8: 31–33
   Google Scholar
• van Breugel H H, Bar P. He-Ne laser irradiation affects proliferation of cultured rat Schwann cells in a dose dependent manner. J Neurocyto 11993; 22: 185-190
   Google Scholar
• Yew DT, Zheng DR, Au C, Li VVW. Responses of astrocytes in culture after low dose laser irradiation. Scann ingMicrosc 1990; 4: 151-158; discussion 158-159
   Google Scholar
• Rochkind S, Barrnea L, Razon N, Bartal A, Schwartz M. Stimulatory effect of He-Ne low dose laser on injured sciatic nerves of rats. Neurosurgery 1987; 20: 843-847
   Google Scholar
• Rochkind S, Ouaknine GE. New trend in neuroscience: Low power laser effecton peripheral and central nervous system (basic science, precl in ical and clinical studies). Neurological Research 1992; 14: 2–11
   PubMedGoogle Scholar
• Rochkind S, Nissan M, Lubart R, Avram J, Bartal A. The in-vivo-nerve response to direct low-energy-laser irradiation. Acta Neurochir 1988; 94: 74-77
   Google Scholar
• Wollman Y, Rochkind S. In vitro cellular processes sprouting in cortex microexplantsof adult rat brains inducedby low power laser irradiation. Neurol Res 1998; 20:470–472
   PubMed Web of Science ®Google Scholar
• Anders JJ, Borke RC, Woolery SK, Van de Merwe WP. Low power laser irradiation alters the rate of regeneration of the rat facial nerve. Laser Surg Med 1993; 13: 72–82
   PubMed Web of Science ®Google Scholar
• Snyder S, Blake K, Dhawan R, Anders JJ, Borke RC, Beebe DC. Quantification of calcitonin gene-related peptide m RNA from cranial nerve nuclei. Soc Neurosci Abstr 1993; 19:254
   Google Scholar
• Snyder S, Byrnes K, Borke RC, Sanchez A, Anders JJ. Quantification of calciton in gene-related peptide m RNA and neuronal cell death in facial motor nuclei following axotomy and 633nm low power laser treatment. Laser Surg Med 2002; 31:216–222
   PubMed Web of Science ®Google Scholar
• Borke RC, Curtis M, Ginsberg C. Choline acetyltransferase and calciton in gene-related peptide im mu noreactivity in motoneurons after differenttypes of nerve injury. J Neurocyto 11993; 22: 141-153
   Google Scholar
• Johnson IP, Duberley RM. Motoneuron survival and expression of neuropeptides and neurotrophic factor receptors following axotomy in adultand ageing rats. Neuroscience 1998; 84: 141-150
   Google Scholar
• Amara SG, Jonas V, Rosenfeld MG, Ong ES, Evans RM. Alternative RNA processing in calcitonin gene expression generates mRNAs encoding different polypeptide products. Nature 1982; 298: 240–244
   PubMed Web of Science ®Google Scholar
• Amara SG, Arriza JL, Leff SE, Swanson LW, Evans RM, Rosenfeld MG. Expression in brain of a messenger RNA encoding a novel neuropeptide homologous to calcitonin gene-related peptide. Science 1985; 229: 1094–1097
   PubMed Web of Science ®Google Scholar
• Noguchi K, Senba E, Morita Y, Sato M, Tohyama M. Alpha-CGRP and beta-CGRP mRNAs are differentially regulated in the rat spinal cord and dorsal root ganglion. Brain Res Mol Brain Res 1990; 7: 299–304
   PubMedGoogle Scholar
• Kruger L, Mantyh PW, Stern ini C, Brecha NC, Mantyh CR. Ca lc ito-ni n gene-related peptide (CG RP) in the rat central nervous system: Patterns of im mu noreactivity and receptor binding sites. Brain Res 1988; 463: 223–244
   PubMed Web of Science ®Google Scholar
• Sarasa M, Terrado J, Mengod G, Climent S, Muniesa P, Palacios JM. Differential expression of alpha-CGRP and beta-CGRP genes within hypoglossal motoneurons in response to axotomy. Brain Res Mol Brain Res 1996; 35:269–277
   PubMedGoogle Scholar
• Haas CA, Streit WJ, Kreutzberg GW. Rat facial motoneurons express increased levels of calciton in gene-related peptide m RNA in response to axotomy. J Neurosci Res 1990; 27:270–275
   PubMed Web of Science ®Google Scholar
• Blake-Bruzzini KM, Borke RC, Anders JJ, Potts JD. Calcitonin gene-related peptide and alpha-CGRP m RNA expression in cranial motoneurons after hypoglossal nerve injury during postnatal developmentJ Neu rocytol 1997; 26: 163–179
   Google Scholar
• Johnson IP, Duberley RM. Motoneuron survival and expression of neuropeptides and neurotrophic factor receptors following axotomy in adultand ageing rats. Neuroscience 1998; 84:141-150
   Google Scholar
• Dai CF, Kanoh N, Li KY, Wang Z. Study on facial motoneuronal death after proximal or distal facial nerve transection. AmJ Otol 2000; 21: 115–118
   PubMedGoogle Scholar
• Yan Q, Matheson C, Lopez OT. In vivo neurotrophic effects of GDNF on neonatal and adult facial motor neurons. Nature 1995; 373:341–344
   PubMed Web of Science ®Google Scholar
• Hottinger AF, Azzouz M, Deglon N, Aebischer P, Zurn AD. Complete and long-term rescue of lesioned adult motoneurons by lentiviral-mediated expression of glial cell line-derived neu-rotrophic factor in the facial nucleus. J Neurosci 2000; 20: 5587–5593
   PubMed Web of Science ®Google Scholar
• Rochkind S, Barr-Nea L, Volger I: Spinal cord response to laser treatment of injured peripheral nerve. Spine 1990; 15: 6–10
   PubMed Web of Science ®Google Scholar
• Rochkind S, Nissan M, Barr-Nea L, Razon N, Schwartz M, Bartal A. Response of peripheral nerve to He-Ne laser: Experimental studies. Laser Surg Med 1987; 7:441–443
   PubMed Web of Science ®Google Scholar
• Shamir MH, Rochkind S, Sandbank J, Alon M. Double-blind randomized study evaluating regeneration of the rat transected sciatic nerve after suturing and postoperative low-power laser treatment.J Reconstr Microsurg 2001; 17: 133–137
   PubMed Web of Science ®Google Scholar
• Rochkind S, Nissan M, Alon M, Shamir M, Salame K. Effects of laser irradiation on the spinal cord for the regeneration of crushed peripheral nerve in rats. Lasers Surg Med 2001; 28: 216–219
   PubMed Web of Science ®Google Scholar
• Miloro M, Halkias LE, Mallery S, Travers S, Rashid RG. Low-level laser effect on neural regeneration in Gore-Tex tubes. Oral Surg Oral Med Oral Pathol Oral Radio/ Endod 2002; 93: 27–34
   PubMed Web of Science ®Google Scholar
• Geuna S, Gigo-Benato D, Tos P, Fornaro M, Battiston B, Giacobini-Robecchi M.G. Nerve regeneration after end-to-side neurorrhaphy is enhanced by post-operative low-power laser biostimulation: an experimental study. In: (Ed. Germann G) Proceedingsof the Second Congress of the World Society of Reconstructive Microsurgery, Heidelberg (Ger), 2003: p.34
   Google Scholar
• Rovak JM, Cederna PS, Kuzon WM Jr. Term ino lateral neurorrhaphy:a review of the literature. J Reconstr Microsurg 2001; 17: 615-624
   Google Scholar
• Wollman Y, Rochkind S, Simantov R. Low power laser irradiation enhances migration and neurite sprouting of cultured rat embryo-nal brain cells. Neurol Res 1996; 18:467–470
   PubMed Web of Science ®Google Scholar
• Wollman Y, Rochkind S. In vitro cellular processes sprouting in cortex microexplantsof adult rat brains induced by low power laser irradiation. Neurol Res 1998; 20: 470–472
   PubMed Web of Science ®Google Scholar
• Shin DH, Lee E, Hyun JK, et al. Growth-associated protein-43 is elevated in the injured rat sciatic nerve after low power laser irradiation. Neurosci Lett 2003; 344: 71-74
   Google Scholar
• Snyder SK, Byrnes KR, Borke RC, Sanchez A, Anders JJ. Quantitation of calcitonin gene-related peptide mRNA and neu-ronal cell death in facial motor nuclei following axotomy and 633 nm low power laser treatment. Lasers Surg Med 2002; 31: 216-222
   Google Scholar
• Leung MC, Lo SC, Siu FK, So KF. Treatment of experimentally induced transient cerebral ischemia with low energy laser inhibits nitric oxide synthase activity and up-regulates the expression of transforming growth factor-beta1. Lasers Surg Med 2002; 31: 283–288
   PubMed Web of Science ®Google Scholar
• Ehrlicher A, Betz T, Stuhrmann B, et al. Guiding neuronal growth with light. Proc Natl Acad Sci USA 2002; 99: 16024–16028
   PubMed Web of Science ®Google Scholar
• Elles JT, Henry, MM, Summerfelt P, et al. Therapeutic photo-biomodulation for methanol-induced retinal toxicity. Proc Nat/ Acad Sci USA 2003; 100:3439–3444
   PubMed Web of Science ®Google Scholar
• Geuna S, Raimondo S, Nicol ino S, etal. Schwann-cell proliferation in muscle-vein combined conduits for bridging rat sciatic nerve defects.J Reconstr Microsurg 2003; 19: 119–123
   Google Scholar
• Alvarez J, Giuditta A, Koenig E. Protein synthesis in axons and terminals: sign ificancefor maintenance, plasticity and regulation of phenotype. With a critique of slow transporttheory. Prog Neurobiol 2000; 62: 1–62
   PubMed Web of Science ®Google Scholar
• Polosukhin VV. Ultrastructure of alveolar macrophages under endobronchial laser therapy of acute and chronic inflammatory lung disease. Immunol Invest 1997; 26:297–311
   PubMed Web of Science ®Google Scholar
• Kreisler M, Christoffers AB, Willershausen B, d'Hoedt B. Effect of low-level GaAlAs laser irradiation on the proliferation rate of human periodontal ligament fibroblasts: An in vitro study. J Clin PeriodontoI 2003; 30: 353-358
   Google Scholar
• Schwartz F, Brodie C, Appel E, Kazimirsky G, ShainbergA. Effect of helium/neon laser irradiation on nerve growth factor synthesis and secretion in skeletal muscle cultures. J Photochem Photobiol B 2002; 66: 195–200
   PubMed Web of Science ®Google Scholar
• Samii M, Carvalho GA, Nikkhah G, Penkert G. Surgical reconstruc-tion of the musculocutaneous nerve in traumatic brachial plexus injuries. J Neurosurg 1997; 87: 881–886
   PubMed Web of Science ®Google Scholar