Influence of clindamycin, metronidazole and polymyxin B on the expression of cell adhesion molecules stimulated by endotoxin and enterotoxin of Bacteroides fragilis

Acta Microbiol Pol. 2003;52(4):361-72.

Abstract

The aim of this study was to compare the influence of antimicrobials (clindamycin, metronidazole and polymyxin B) on the expression of adhesion molecules (VCAM-1, ICAM-1 and E-selectin) on the HMEC-1 cell line stimulated by LPS and enterotoxin of B. fragilis. LPS was extracted from two reference: ATCC 43858 and NCTC 11295 and one isolated in our laboratory (W2) enterotoxigenic strains, and one nonenterotoxigenic reference strain--IPL E 323. Enterotoxin preparations (Tox 1 and Tox 2) were isolated from supematant of B. fragilis ATCC 43858 culture and purified. HMEC-1 cell line was stimulated with bacterial preparations at concentration of 10 mg/ml. For measuring the expression of adhesion molecules we used ELISA test. Clindamycin, metronidazole and polymyxin B supressed the ICAM-1 expression when endothelium was stimulated with B. fragilis LPS and augmented ICAM-1 expression by Tox 1 and Tox 2. The expression of VCAM-1 was augmented by antimicrobials when endothelium was stimulated with LPS or enterotoxin preparations. The expression of E-selectin was differentiated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / pharmacology*
  • Bacteroides fragilis / metabolism*
  • Cell Line
  • Clindamycin / pharmacology
  • E-Selectin / biosynthesis
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / metabolism*
  • Endothelium, Vascular / microbiology
  • Endotoxins / pharmacology*
  • Humans
  • Intercellular Adhesion Molecule-1 / biosynthesis*
  • Metalloendopeptidases / pharmacology
  • Metronidazole / pharmacology
  • Polymyxin B / pharmacology
  • Vascular Cell Adhesion Molecule-1 / biosynthesis*

Substances

  • Anti-Bacterial Agents
  • E-Selectin
  • Endotoxins
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • Metronidazole
  • Clindamycin
  • Metalloendopeptidases
  • fragilysin
  • Polymyxin B