[The effect of bactericidal/permeability-increasing protein on lipopolysaccharide-binding protein and lipopolysaccharide receptor CD14 mRNA expression in rats after thermal injury]

Zhonghua Yi Xue Za Zhi. 1999 Apr;79(4):289-91.
[Article in Chinese]

Abstract

Objective: To elucidate the possible mechanisms underlying beneficial effect of recombinant bactericidal/permeability-increasing protein (rBPI) on multiple organ damage secondary to major burns.

Methods: Wistar rats were subjected to a 35% full-thickness scald injury, and randomly divided into 3 groups: normal controls (n = 8), thermal injury (n = 21), and rBPI21 treatment (n = 12). In thermal injury and rBPI21 treatment groups, animals were sacrificed at 12 and 24 hours after burn, respectively. Tissue samples from liver, kidneys, lungs and intestine were collected to measure lipopolysaccharide-binding protein (LBP)/lipopolysaccharide receptor CD14 and tumor necrosis factor-alpha (TNF-alpha) mRNA expression. In addition, blood samples were obtained for measurement of organ function parameters.

Results: Treatment with rBPI21 could significantly decrease tissue LBP and CD14 mRNA expression in various organs (P < 0.05-0.01). Also, TNF-alpha mRNA expression in liver, kidneys and lungs were markedly inhibited by rBPI21 secondary to acute insults (P < 0.05-0.01). Moreover, in the rBPI21 treatment group, significant reduction in serum GPT levels and elevation in intestinal DAO activities were found compared to those in the thermal injury group (P < 0.05-0.01).

Conclusions: Treatment with rBPI21 is effective in attenuating multiple organ damage resulted from gut origin endotoxin translocation after thermal injury, which might be associated with down-regulation effect of tissue LBP and CD14 gene expression by use of rBPI21.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins*
  • Animals
  • Anti-Infective Agents / pharmacology
  • Antimicrobial Cationic Peptides
  • Bacterial Translocation
  • Blood Proteins / pharmacology*
  • Burns / metabolism*
  • Carrier Proteins / biosynthesis*
  • Carrier Proteins / genetics
  • Down-Regulation
  • Lipopolysaccharide Receptors / biosynthesis*
  • Lipopolysaccharide Receptors / genetics
  • Lipopolysaccharides / metabolism
  • Male
  • Membrane Glycoproteins*
  • Membrane Proteins*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Rats
  • Rats, Wistar

Substances

  • Acute-Phase Proteins
  • Anti-Infective Agents
  • Antimicrobial Cationic Peptides
  • Blood Proteins
  • Carrier Proteins
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • Membrane Proteins
  • RNA, Messenger
  • bactericidal permeability increasing protein
  • lipopolysaccharide-binding protein