Growth of nerve fibres into murine peritoneal adhesions

J Pathol. 2000 Nov;192(3):396-403. doi: 10.1002/1096-9896(2000)9999:9999<::AID-PATH710>3.0.CO;2-4.

Abstract

Adhesions in the peritoneal cavity have been implicated in the cause of intestinal obstruction and infertility, but their role in the aetiology of chronic pelvic pain is unclear. Nerves have been demonstrated in human pelvic adhesions, but the presence of pain-conducting fibres has not been established. The purpose of this study was to use an animal model to examine the growth of nerves during adhesion formation at various times following injury and to characterize the types of fibres present. Adhesions were generated in mice by injuring the surface of the caecum and adjacent abdominal wall, with apposition. At 1-8 weeks post-surgery, adhesions were processed and nerve fibres characterized histologically, immunohistochemically, and ultrastructurally. Peritoneal adhesions had consistently formed by 1 week after surgery and from 2 weeks onwards, all adhesions contained some nerve fibres which were synaptophysin, calcitonin gene-related peptide, and substance P-immunoreactive, and were seen to originate from the caecum. By 4 weeks post-surgery, nerve fibres were found to originate from both the caecum and the abdominal wall, and as demonstrated by acetylcholinesterase histochemistry, many traversed the entire adhesion. Ultrastructural analysis showed both myelinated and non-myelinated nerve fibres within the adhesion. This study provides the first direct evidence for the growth of sensory nerve fibres within abdominal visceral adhesions in a murine model and suggests that there may be nerve fibres involved in the conduction of pain stimuli.

MeSH terms

  • Abdominal Muscles / innervation
  • Acetylcholinesterase / physiology
  • Animals
  • Calcitonin Gene-Related Peptide / immunology
  • Cecum / innervation
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Electron
  • Models, Biological
  • Nerve Fibers / pathology
  • Peritoneal Diseases / immunology
  • Peritoneal Diseases / pathology*
  • Substance P / immunology
  • Synaptophysin / immunology
  • Tissue Adhesions / immunology
  • Tissue Adhesions / pathology

Substances

  • Synaptophysin
  • Substance P
  • Acetylcholinesterase
  • Calcitonin Gene-Related Peptide