Abstract

Peripheral nerve injury is a life-changing disability with significant socioeconomic consequences. In this rat model, we propose that partial enzyme digestion can facilitate the functional recovery of a crushed nerve. The sciatic nerves were harvested and in vitro cultured with the addition of Liberase to determine the appropriate enzyme amount in the hyaluronic acid (HA) membrane. Then, the sciatic nerve of adult male Sprague-Dawley rats was exposed, crushed, and then treated with partial enzyme digestion (either 0.001 or 0.002 unit/mm2 Liberase-HA membrane). The sciatic function index (SFI) for functional recovery of the sciatic nerve was evaluated. After 2 h of in vitro digestion, fascicles and axons were separated from each other, with the cells mobilized. Greater destruction of histology structures occurred in the high enzyme (Liberase-HA membrane at 0.002 unit/mm2) group at 24 h than in the low enzyme (0.001 unit/mm2) group at 48 h. In the SFI evaluation, the improvement in 0.001 unit/mm2 Liberase group was significantly better than control and 0.002 unit/mm2 Liberase group. Our study demonstrated that appropriate enzyme digestion had a significantly faster and earlier recovery.

Highlights

  • Peripheral nerve injury (PNI) is a life-changing disability with significant socioeconomic consequences

  • After 20 days’ culture, the dishes were rinsed with phosphate-buffered saline (PBS, Sigma-Aldrich Co.), and the cell clusters were rinsed with 1 mL of iced DMEM to separate the Schwann cells (SCs) from the firmly attached fibroblasts

  • Differences were considered significant at p < 0.05

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Summary

Introduction

Peripheral nerve injury (PNI) is a life-changing disability with significant socioeconomic consequences. When compared with the central nervous system (CNS), the peripheral nerve has a greater ability to repair or regenerate after injury, it remains a clinical challenge to restore normal function [1,2,3]. The restoration of nerve function is mainly dependent on the re-growth of the nerve itself. Schwann cells (SCs) form bands of Büngner, secrete neurotrophic growth factors, and support axonal regeneration and re-myelination [4]. In this process, SCs can facilitate nerve regeneration; while the excessive extracellular matrix (ECM) and growth of fibrotic tissue during nerve regeneration impede their abilities of nerve regeneration

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