Prevention of intraperitoneal adhesions and abscesses by polysaccharides isolated from Phellinus spp in a rat peritonitis model

Ann Surg. 2005 Mar;241(3):534-40. doi: 10.1097/01.sla.0000154281.79639.89.

Abstract

Objective: To assess whether polysaccharides isolated from fungi, Phellinus spp, could reduce the adhesion and abscess formation in a rat peritonitis model.

Summary background data: Although polysaccharides from Phellinus spp is a well-known material with antiinflammatory properties, little is known regarding its ability to prevent intraperitoneal adhesions. We have assessed the adhesion- and abscess-reducing effect of polysaccharides from Phellinus gilvus (PG) and Phellinus linteus (PL) in a rat peritonitis model.

Methods: In 60 SD rats, experimental peritonitis was induced using the cecal ligation and puncture model (CLP). Animals were randomly assigned to 5 groups; ringer lactate solution (RL group), polysaccharides from PG and PL (PG and PL group), hyaluronic acid (HA group), and carboxymethylcellulose (CMC group). Intraperitoneal adhesions and abscesses were noted at 7 day after CLP. RT-PCR assay for urokinase-type plasminogen activator (uPA), its cellular receptor (uPAR), tissue-type plasminogen activator (tPA), plasminogen activator inhibitor type 1 (PAI-1), and tumor necrosis factor (TNF)- alpha was performed to assess the cecal tissue.

Results: Adhesion formation was significantly reduced in PG, PL, CMC, and HA groups (P < 0.001) compared with that in RL group. The incidence of abscesses was also significantly reduced in PG and PL groups (P < 0.05) compared with that in the RL group. The level of uPA, uPAR, tPA, and TNF-alpha was highly expressed in PG and PL group, as compared with the RL group.

Conclusions: We concluded that PG and PL had significant adhesion- and abscess-reducing effects and may act by modulating fibrinolytic capacity of uPA and/or tPA produced from macrophages in a rat peritonitis model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Abscess / etiology
  • Abdominal Abscess / microbiology
  • Abdominal Abscess / prevention & control*
  • Animals
  • Ascitic Fluid / microbiology
  • Basidiomycota*
  • Carboxymethylcellulose Sodium / therapeutic use
  • Cecum / chemistry
  • Hyaluronic Acid / therapeutic use
  • Male
  • Peritonitis / complications*
  • Peritonitis / metabolism
  • Peritonitis / microbiology
  • Plasminogen Activator Inhibitor 1 / analysis
  • Polysaccharides / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Cell Surface / analysis
  • Receptors, Urokinase Plasminogen Activator
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tissue Adhesions / etiology
  • Tissue Adhesions / pathology
  • Tissue Adhesions / prevention & control*
  • Tissue Plasminogen Activator / analysis
  • Tumor Necrosis Factor-alpha / analysis
  • Urokinase-Type Plasminogen Activator / analysis

Substances

  • Plasminogen Activator Inhibitor 1
  • Plaur protein, rat
  • Polysaccharides
  • Receptors, Cell Surface
  • Receptors, Urokinase Plasminogen Activator
  • Tumor Necrosis Factor-alpha
  • Hyaluronic Acid
  • Tissue Plasminogen Activator
  • Urokinase-Type Plasminogen Activator
  • Carboxymethylcellulose Sodium