Fibrin Sealant Matrix Supports Outgrowth of Peripheral Sensory Axons

References

• Aebischer P, Guenard V, Valentini RE. The morphology of regenerating peripheral nerves is modulated by the surface microgeometry of polymeric guidance channels. Brain Res 1990; 531: 211–218
   PubMed Web of Science ®Google Scholar
• Arntz C, Kanje M, Lundborg G. Regeneration of the rat sciatic nerve after different conditioning lesions: effects of the conditioning interval. Microsurgery 1989; 10: 118
   PubMed Web of Science ®Google Scholar
• Danielsen N, Müller H, Pettmann B, et al. Rat amnion membrane matrix as a substratum for regenerating axons from peripheral and central neurons: effects in a silicone chamber model. Dev Brain Res 1988; 39: 39–50
   Google Scholar
• Fields RD, Le Beau JM, Longo FM, Ellisman MH. Nerve regeneration through artificial tubular implants. Prog Neurobiol 1989; 33: 87–134
   PubMed Web of Science ®Google Scholar
• Gibble JW, Ness PM. Fibrin glue: the perfect operative sealant. Transfusion 1990; 30: 741–747
   PubMed Web of Science ®Google Scholar
• Gillery P, Bellon G, Coustry F, Borel JP. Cultures of fibroblasts in fibrin lattices: Models for the study of metabolic activities of the cells in physiological conditions. J Cell Physiol 1989; 140: 483–490
   PubMed Web of Science ®Google Scholar
• Jeng CB, Coggshall RE. Nerve regeneration through holey silicone tubes. Brain Res 1985; 361: 233–241
   PubMed Web of Science ®Google Scholar
• Konorski J, Lubinska L. Mechanical excitability or regenerating nerve fibres. Lancet 1946; 27: 609
   Google Scholar
• Krystosek A, Seeds NW. Plaminogen activator release at the neuronal growth cone. Science 1981; 213: 1532–1534
   PubMed Web of Science ®Google Scholar
• Krystosek A, Seeds NW. Peripheral neurons and Schwann cells secrete plasminogen activator. J Cell Biol 1984; 98: 773–776
   PubMed Web of Science ®Google Scholar
• Le Beau JM, Ellisman MH, Powell HC. Ultra-structural and morphometric analysis of long-term peripheral nerve regeneration through silicone tubes. J Neurocytol 1988; 17: 161–172
   Google Scholar
• Letourneau PC. Cell-substratum adhesion of neurite growth cones and its role in neurite elongation. Exp Cell Res 1979; 124: 127–138
   PubMed Web of Science ®Google Scholar
• Lerner R, Binur NS. Current Research Review: Current status of surgical status of surgical adhesives. J Surg Res 1990; 48: 165–181
   Google Scholar
• Longo FM, Hayman EG, Davis GE, et al. Neurite-promoting factors and extracellular matrix components accumulating in vivo within nerve regeneration chambers. Brain Res 1984; 309: 105–117
   PubMed Web of Science ®Google Scholar
• Lundborg G. Nerve injury and repair: Nerve regeneration. Churchill Livingstone, Edinburgh 1988; 149–195
   Google Scholar
• Matras H, Dinges HP, Lassmann H, Mamoli B. Zur nahtlosen interfaszikulären Nerventrans-plantation im Tierexperiment. Wien Med Woch-enschr 1972; 122: 517
   PubMedGoogle Scholar
• Rogers SL, McCarthy JB, Palm SL, Furcht LT, Letourneau PC. Neuron-specific interactions with two neurite-promoting fragments of fibronectin. J Neurosci 1985; 5: 369–378
   PubMed Web of Science ®Google Scholar
• Redl H, Schlag G. Fibrin sealant and its modes of application. Fibrin sealant in operative medicine, G Schlag, H Redl. Springer Verlag, Heidelberg 1986; Vol. 1: 13–26
   Google Scholar
• Schlag G, Redl H, Turnher M, Dinges HP. Fibrin sealant in operative medicine: The importance of fibrin sealant in wound repair, G Schlag, H Redl. Springer-Verlag, Heidelberg 1986; Vol. 1: 3–10
   Google Scholar
• Schlag G, Redl H. Fibrin sealant in orthopedic surgery. Clin Orthop 1988; 27: 269
   Google Scholar
• Schlag G, Redl H. Wound healing: fibrin sealing in surgical and nonsurgical fields. Springer-Verlag, Heidelberg 1994; Vol. 1: 3–145
   Google Scholar
• Sonnentag H, Rösner H, Rahmann H. Influence of exogenous gangliosides on the three-dimensional sprouting of goldfish retinal explants in vitro. Neurochem Res 1992; 17: 1105–1112
   Google Scholar
• Williams LR, Longo FM, Powell HC, Lundborg G, Varon S. Spatial-temporal progress of peripheral nerve regeneration within a silicone chamber: Parameters for a bioassay. J Comp Neurol 1983; 218: 460–470
   PubMed Web of Science ®Google Scholar
• Williams LR, Varon S. Modification of fibrin matrix formation in situ enhances nerve regeneration in silicone chambers. J Comp Neurol 1985; 231: 209–220
   PubMed Web of Science ®Google Scholar
• Williams LR. Exogenous fibrin matrix precursors stimulate the temporal progress of nerve regeneration within a silicone chamber. Neurochem Res 1987; 12: 851–860
   PubMed Web of Science ®Google Scholar
• Williams LR, Danielsen N, Muller H, Varon S. Exogenous matrix precursors promote functional nerve regeneration across a 15-mm gap within a silicone chamber in the rat. J Comp Neurol 1987; 264: 284–190
   PubMed Web of Science ®Google Scholar
• Weiss P. Sutureless reunion of severed nerves with elastic cuffs of tantalum. J Neurosurg 1944; 1: 219
   Google Scholar
• Young JZ, Medawar PB. Fibrin suture of peripheral nerves. Measurement of the rat of regeneration. Lancet 1940; 2: 126
   Google Scholar
• Zeng L, Leichtfried G, Dinges HP, Schlag G, Redl H. An experimental study of peripheral nerve repair with a biodegradable neurotropic and neurotrophic matrix. J Reconstr Microsurg 1994; 10: 53
   Google Scholar
• Zeng L, Worseg A, Redl H, Schlag G. An experimental study of peripheral nerve repair with nerve growth factor and fibrin matrix. Eur J Plast Surg 1994; 17: 228–232
   Google Scholar
• Zeng L, Huck S, Mallinger R, Redl H, Schlag G. Fibrin matrix substratum supports neurite outgrowth of chick sensory neurons in vitro. Eur J Neurosci Suppl 1994; 7: 40
   Google Scholar
• Zhao G, Dahlin LB, Kanje M, Lundborg G. Repair of the transected rat sciatic nerve: Matrix formation with silicone tubes. Restor Neurol Neurosci 1993; 5: 197–204
   PubMed Web of Science ®Google Scholar