Detergent-based decellularized peripheral nerve allografts: An in vivo preclinical study in the rat sciatic nerve injury model
Metadatos
Mostrar el registro completo del ítemAutor
Chato Astrain, Jesús; Philips, Charlot; Campos Sánchez, Fernando; Durand Herrera, Daniel; García García, Óscar Darío; Roosens, Annelies; Alaminos Mingorance, Miguel; Campos Muñoz, Antonio Jesús; Carriel Araya, VíctorEditorial
Wiley
Materia
Chemical decellularization Functional recovery Histology Nerve repair Peripheral nerve regeneration Tissue engineering
Fecha
2020-02Referencia bibliográfica
Chato-Astrain J, Philips C, Campos F, et al. Detergent-based decellularized peripheral nerve allografts: An in vivo preclinical study in the rat sciatic nerve injury model. J Tissue Eng Regen Med. 2020;14:789–806. https://doi.org/10.1002/term.3043
Patrocinador
Instituto de Salud Carlos III: FIS PI17/0393, FIS PI17-0393; FEDER Andalucía 2014-2020, I +D +I, A-CTS-488-UGR18Resumen
Nerve autograft is the gold standard technique to repair critical nerve defects, but efficient alternatives are needed. The present study evaluated the suitability of our novel Roosens-based (RSN) decellularized peripheral nerve allografts (DPNAs) in the repair of 10-mm sciatic nerve defect in rats at the functional and histological levels after 12 weeks. These DPNAs were compared with the autograft technique (AUTO) and Sondell (SD) or Hudson (HD) based DPNAs. Clinical and functional assessments demonstrated a partial regeneration in all operated animals. RSN-based DPNAs results were comparable with SD and HD groups and closely comparable with the AUTO group without significant differences (p > .05). Overall hematological studies confirmed the biocompatibility of grafted DPNAs. In addition, biochemistry revealed some signs of muscle affection in all operated animals. These results were confirmed by the loss of weight and volume of the muscle and by muscle histology, especially in DPNAs. Histology of repaired nerves confirmed an active nerve tissue regeneration and partial myelination along with the implanted grafts, being the results obtained with HD and RSN-based DPNAs comparable with the AUTO group. Finally, this in vivo study suggests that our novel RSN-based DPNAs supported a comparable tissue
regeneration, along the 10-mm nerve gap, after 12-week follow-up to HD DPNAs, and both were superior to SD group and closely comparable with autograft technique. However, further improvements are needed to overcome the efficacy of the nerve autograft technique.





