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Use of chemically extracted muscle grafts to repair extended nerve defects in rats

Författare

Summary, in English

Nerve regeneration, measured as axonal outgrowth, Schwann cell migration, macrophage invasion, and neovascularisation, was compared after repair of a 15 mm gap in rats' sciatic nerves using autologous muscle grafts made acellular either by freezing and thawing or by chemical extraction. Both extracted and freeze-thawed acellular muscle grafts could be used to bridge the defect. However, axons and Schwann cells, as shown by immunohistochemical staining for neurofilaments and S-100 protein, respectively, grew faster into the extracted muscle grafts than into the freeze-thawed acellular muscle grafts and somewhat more axons were observed in the former graft. There were no significant differences between the two graft types with respect to neovascularisation as showed by staining for endothelial alkaline phosphatase, and limited differences concerning invasion of macrophages (ED1 and ED2) as detected by immunocytochemistry. The results showed that chemically extracted muscle grafts could be used to bridge an extended nerve defect and that such grafts in some aspects were superior to freeze-thawed muscle grafts for extended gaps.

Publiceringsår

2001

Språk

Engelska

Sidor

337-345

Publikation/Tidskrift/Serie

Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery

Volym

35

Issue

4

Dokumenttyp

Artikel i tidskrift

Förlag

Taylor & Francis

Ämne

  • Surgery

Nyckelord

  • Muscle
  • Graft
  • Acellular
  • Nerve
  • Regeneration
  • Schwann
  • Cell
  • Macrophages
  • Immunocytochemistry
  • Axons
  • Repair

Status

Published

Forskningsgrupp

  • Hand Surgery, Malmö

ISBN/ISSN/Övrigt

  • ISSN: 1651-2073