Use of hybrid chitosan membranes and N1E-115 cells for promoting nerve regeneration in an axonotmesis rat model

被引:98
作者
Amado, S. [2 ]
Simoes, M. J. [3 ,4 ]
da Silva, P. A. S. Armada [2 ]
Luis, A. L. [3 ,4 ]
Shirosaki, Y. [5 ]
Lopes, M. A. [5 ]
Santos, J. D. [5 ]
Fregnan, F. [6 ]
Gambarotta, G. [6 ]
Raimondo, S. [1 ]
Fornaro, M. [1 ]
Veloso, A. P. [2 ]
Varejao, A. S. P. [7 ]
Mauricio, A. C. [3 ,4 ]
Geuna, S. [1 ]
机构
[1] Univ Turin, Osped San Luigi, Dept Clin & Biol Sci, I-10043 Orbassano, TO, Italy
[2] Univ Tecn Lisboa, Fac Human Kinet, P-1100 Lisbon, Portugal
[3] Univ Porto, Anim Sci & Study Ctr CECA, Food & Agr Sci & Technol Inst ICETA, P-4100 Oporto, Portugal
[4] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Dept Vet Clin, P-4100 Oporto, Portugal
[5] Univ Porto, Fac Engn, P-4100 Oporto, Portugal
[6] Univ Turin, Dept Human & Anim Biol, Turin, Italy
[7] Univ Tras Os Montes & Alto Douro, Dept Vet Sci, CITAB, Vila Real, Portugal
关键词
Nerve; Nerve regeneration; Nerve tissue engineering; Chitosan; Animal model;
D O I
10.1016/j.biomaterials.2008.07.043
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Many studies have been dedicated to the development of scaffolds for improving post-traumatic nerve regeneration. The goal of this study was to develop and test hybrid chitosan membranes to use in peripheral nerve reconstruction, either alone or enriched with N1E-115 neural cells. Hybrid chitosan membranes were tested in vitro, to assess their ability in supporting N1E-115 cell survival and differentiation, and in vivo to assess biocompatibility as well as to evaluate their effects on nerve fiber regeneration and functional recovery after a standardized rat sciatic nerve crush injury. Functional recovery was evaluated using the sciatic functional index (SFI), the static sciatic index (SSI), the extensor postural thrust (EFT), the withdrawal reflex latency (WRL) and ankle kinematics. Nerve fiber regeneration was assessed by quantitative stereological analysis and electron microscopy. All chitosan membranes showed good biocompatibility and proved to be a suitable substrate for plating the N1E-115 cellular system. By contrast, in vivo nerve regeneration assessment after crush injury showed that the freeze-dried chitosan type III. without N1E-115 cell addition, was the only type of membrane that significantly improved posttraumatic axonal regrowth and functional recovery. it can be thus suggested that local enwrapping with this type of chitosan membrane may represent an effective approach for the improvement of the clinical outcome in patients receiving peripheral nerve surgery. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4409 / 4419
页数:11
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