Abstract

Introduction: Primate animal models are being utilized to explore novel therapies for spinal cord injuries. This study aimed to evaluate the efficiency of the transplantation of predegenerated nerve segments in unilateral spinal cord-hemisected bonnet monkeys’ (Macaca radiata) locomotor functions using the complex runways. Materials and Methods: The bonnet monkeys were initially trained to walk in a bipedal motion on grid and staircase runways. In one group of trained monkeys, surgical hemisection was made in the spinal cord at the T12-L1 level. In the other group, hemisection was induced in the spinal cord, and the ulnar nerve was also transected at the same time (transplant group). After one week, the hemisected cavity was reopened and implanted with predegenerated ulnar nerve segments obtained from the same animal of the transplant group. Results: All the operated monkeys showed significant deficits in locomotion on runways at the early postoperative period. The walking ability of operated monkeys was found to be gradually improved, and they recovered nearer to preoperative level at the fourth postoperative month, and there were no marked differences. Conclusion: The results demonstrate that there were no significant improvements in the locomotion of monkeys on runways after the delayed grafting of nerve segments until one year later. The failure of the predegenerated nerve graft as a possible therapeutic strategy to improve the locomotion of monkeys may be due to a number of factors set in motion by trauma, which could possibly prevent the qualities of regeneration. The exact reason for this ineffectiveness of predegenerated nerve segments and their underlying mechanism is not known.

Highlights

  • Primate animal models are being utilized to explore novel therapies for spinal cord injuries

  • Several transplants, such as embryonic neural tissue [1,2], peripheral nerve tissue [3,4], and Schwann cells [5,6] are commonly used as a therapeutic approach to repair spinal cord (SC) injuries (SCI), which differ by their nature, origin, and mode of action

  • The present study demonstrates that transplantation of predegenerated peripheral

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Summary

Introduction

Primate animal models are being utilized to explore novel therapies for spinal cord injuries. Impairment/injury in the spinal cord (SC) in mammals usually causes temporary or permanent paraplegia based on the severity of the injury Several transplants, such as embryonic neural tissue [1,2], peripheral nerve tissue [3,4], and Schwann cells [5,6] are commonly used as a therapeutic approach to repair SC injuries (SCI), which differ by their nature, origin, and mode of action. Many scientists in SC injury research were attracted to the use of the peripheral nerve graft (PNG) as a possible means for promoting SC repair This may be due to the well-known fact that the use of embryonic neural tissue for transplantation is difficult to obtain but has inherent ethical problems to use in patients. All types of transplants can stimulate the growth of axons from host nerve fibers, but these actions are far more important and conspicuous with PNG [9,10], which provides a favorable atmosphere for the growth of axons and provides guidance by directing the regrowth of fibers to a specific target [11]

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