Long‐term neural regeneration following injury to the peroneal branch of the sciatic nerve in sheep

• Published in: The European journal of neuroscience 2020-11, Vol.52 (10), p.4385-4394
• Main Authors: Roballo, Kelly C.S., Burns, Daniel T., Ghnenis, Adel B., Osimanjiang, Wupu, Bushman, Jared S.
• Format: Article
• Language: English
• Subjects: Animal models; axon regeneration; Body weight; Fibrosis; large animal model; Morphometry; peripheral nerve injury; peripheral nerve regeneration; peripheral nerve surgery; Peripheral nerves; Regeneration; Sciatic nerve; Sheep; Surgery; Trauma
• ISSN: 0953-816X; 1460-9568
• DOI: 10.1111/ejn.14835

Peripheral nerves (PNs) are frequently injured as a result of trauma or disease. Development of therapies to regenerate PNs requires the use of animal models, typically beginning in rodents and progressing to larger species. There are several large animal models of PN regeneration that each has their benefits and drawbacks. Sheep have been used in PN studies due to their similarities in body weight to humans and the ease and lesser expense in their care and housing relative to other species. We have investigated the use of sheep for studies of PN regeneration and have developed and tested an injury model in the peroneal branch of the sciatic nerve. Three experimental groups were tested on mature sheep: a bisection; a 5‐cm reverse autograft; and sham surgery. Protocols were developed for the post‐operative care for animals with this injury, and regeneration was tracked for extended time points via compound muscle action potentials (CMAPs) and endpoint assessments of nerve morphometry, muscle mass and muscle fibrosis. Results indicate the practical viability of this PN injury model and show distinctions in the degree and rate of regeneration between bisection and reverse autograft that persisted 14 months. This long‐term study shows bisections lead to significantly improved CMAPS and muscle mass and lesser muscle fibrosis as compared to reverse autograft. The persistence of these discernable changes between two relatively similar experimental groups out to extended time points is an indication of the sensitivity of this nerve section and its potential applicability for comparative studies. Development of therapies to regenerate peripheral nerves (PN) requires the use of animal models, typically beginning in rodents and progressing to larger species. In the present study, we have investigated the use of sheep for studies of PN regeneration and have developed and tested an injury model in the peroneal branch of the sciatic nerve in a long term study (14 months).