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Cell Tissue Bank. 2019 Jun;20(2):307-319. doi: 10.1007/s10561-019-09770-x. Epub 2019 Apr 27.

Comparison of the regeneration induced by acellular nerve allografts processed with or without chondroitinase in a rat model.

Author information

1
Department of Orthopedic Surgery, Gyeongsang National University Changwon Hospital, Changwon, Korea.
2
Department of Orthopedic Surgery, The Catholic University of Korea College of Medicine, Seoul, Korea. jylos1@gmail.com.
3
Korea Public Tissue Bank, Seoul, Korea.
4
Department of Orthopedic Surgery, The Catholic University of Korea College of Medicine, Seoul, Korea.

Abstract

There have been various studies about the acellular nerve allograft (ANA) as the alternative of autologous nerve graft in the treatment of peripheral nerve defects. As well as the decellularization process methods of ANA, the various enhancement methods of regeneration of the grafted ANA were investigated. The chondroitin sulfate proteoglycans (CSPGs) inhibit the action of laminin which is important for nerve regeneration in the extracellular matrix of nerve. Chondroitinase ABC (ChABC) has been reported that it enhances the nerve regeneration by degradation of CSPGs. The present study compared the regeneration of ANA between the processed without ChABC group and the processed with ChABC group in a rat sciatic nerve 15 mm gap model. At 12 weeks postoperatively, there was not a significant difference in the histomorphometric analysis. In the functional analysis, there were no significant differences in maximum isometric tetanic force, wet muscle weight of tibialis anterior. The processed without ChABC group had better result in ankle contracture angle significantly. In conclusion, there were no significant differences in the regeneration of ANA between the processed without ChABC group and the processed with ChABC group.

KEYWORDS:

Acellular nerve allograft; Chondroitin sulfate proteoglycans; Chondroitinase; Peripheral nerve regeneration; Processed nerve allograft; Rat model

PMID:
31030290
DOI:
10.1007/s10561-019-09770-x
[Indexed for MEDLINE]

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