Abstract

The regenerative capability of peripheral nerves is very limited, and several strategies have been proposed to increase nerve regeneration. In the present work, we have analyzed the in vivo usefulness of a novel nanostructured fibrin-agarose bio-artificial nerve substitute (Nano) used alone or in combination with NeuraGen® collagen type I conduits (Coll-Nano) in laboratory rats with a 10-mm sciatic nerve defect. Control animals were subjected to the gold-standard autograft technique (Auto). Results first demonstrated that the percentage of self-amputations was lower in Nano and Coll-Nano groups as compared to the Auto group. Neurotrophic ulcers were more abundant in the Auto group (60%, with 66.6% of them being >2-mm) than Nano and Coll-Nano groups (0%) at 4 weeks, although Nano showed more ulcers after 12 weeks. Foot length was significantly altered in Auto animals due to neurogenic retraction, but not in Nano and Coll-Nano groups after 12 weeks. At the functional level, all animals showed a partial sensory recovery as determined by the pinch test, especially in Nano and Auto groups, but did not reach the levels of native animals. Toe-spread test revealed a partial motor function recovery only in Nano animals at 4 weeks and Auto and Nano at 12 weeks. Electromyography showed clear denervation signs in all experimental groups, with few differences between Auto and Nano animals. After 12 weeks, an important denervation decrease and an increase of the reinnervation process was found in Auto and Nano groups, with no differences between these groups. Histological analyses demonstrated an active peripheral nerve regeneration process with newly formed peripheral nerve fascicles showing S-100, GAP-43 and myelin in all experimental groups. The peripheral nerve regeneration process was more abundant in Auto group, followed by Nano group, and both were better than Coll-Nano group. Muscle histology confirmed the electromyography results and showed some atrophy and fibrosis signs and an important weight and volume loss in all groups, especially in the Coll-Nano group (56.8% weight and 60.4% volume loss). All these results suggest that the novel Nano substitutes used in in vivo were able to contribute to bridge a 10-mm peripheral nerve defect in rats.

Highlights

  • Peripheral nerves (PNs) are delicate organs which form a highly complex network throughout the body connecting the central nervous system with distal target organs (Topp and Boyd, 2006; Carriel et al, 2014a)

  • Regarding the Coll-nanostructured fibrin-agarose bio-artificial nerve substitute (Nano) group, the nanostructured fibrin-agarose bio-artificial nerve substitutes (NFABNS) were incorporated as intraluminal fillers of collagen conduits during surgery, and the defects were repaired by using the conventional tubulization technique without any technical inconvenience

  • After 14 weeks of in vivo implantation the autograft technique (Auto) group showed a complete repair of the defects without any sign of structural damage, a loose connective tissue was observed covering the repaired area (Figure 2)

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Summary

Introduction

Peripheral nerves (PNs) are delicate organs which form a highly complex network throughout the body connecting the central nervous system with distal target organs (Topp and Boyd, 2006; Carriel et al, 2014a). PNs are composed by the nerve tissue or parenchyma and three specialized connective tissue layers or stroma (Geuna et al, 2009; Carriel et al, 2014a). The parenchyma is organized in conductive units called peripheral nerve fibers (PNFs) internally formed by neuronal axons surrounded by Schwann cells (SCs) and a thin external basal lamina. PNs are externally covered by a collagen-rich and vascularized connective tissue layer, the epineurium. At the intrafascicular level, each PNF is surrounded by a loose connective tissue, the endoneurium (Topp and Boyd, 2006; Geuna et al, 2009; Carriel et al, 2014a, 2017a)

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