2017
DOI: 10.4274/balkanmedj.2015.1601
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Can a Small Intestine Segment Be an Alternative Biological Conduit for Peripheral Nerve Regeneration?

Abstract: Background:Autologous nerve grafts are used to bridge peripheral nerve defects. Limited sources and donor site morbidity are the major problems with peripheral nerve grafts. Although various types of autologous grafts such as arteries, veins and muscles have been recommended, an ideal conduit has not yet been described.Aims:To investigate the effectiveness of a small intestinal conduit for peripheral nerve defects.Study Design:Animal experimentation.Methods:Twenty-one rats were divided into three groups (n=7).… Show more

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Cited by 5 publications
(1 citation statement)
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“…Desirable features of NGCs include biocompatibility with the surrounding tissue, flexibility, the ability to be sutured into the injury site, and the incorporation of chemotactic, structural, and topographical cues for directional axonal regeneration [3,4]. Tissue derived NGCs have included autologous transplants of skeletal muscle, with its basal lamina and anisotropy, tendon, and vein [5], or rinsed small intestinal segments [6], with each displaying variable abilities to repair peripheral nerve lesions. Decellularised nerve allografts have shown promise in bridging small gap injuries [1,2] and, whilst they contain tissue specific ECM, they lack the necessary cellular support required for regeneration across long gaps [2,7].…”
Section: Introductionmentioning
confidence: 99%
“…Desirable features of NGCs include biocompatibility with the surrounding tissue, flexibility, the ability to be sutured into the injury site, and the incorporation of chemotactic, structural, and topographical cues for directional axonal regeneration [3,4]. Tissue derived NGCs have included autologous transplants of skeletal muscle, with its basal lamina and anisotropy, tendon, and vein [5], or rinsed small intestinal segments [6], with each displaying variable abilities to repair peripheral nerve lesions. Decellularised nerve allografts have shown promise in bridging small gap injuries [1,2] and, whilst they contain tissue specific ECM, they lack the necessary cellular support required for regeneration across long gaps [2,7].…”
Section: Introductionmentioning
confidence: 99%