Treatment with the hyaluronic acid synthesis inhibitor 4-methylumbelliferone suppresses SEB-induced lung inflammation

Toxins (Basel). 2013 Oct 17;5(10):1814-26. doi: 10.3390/toxins5101814.

Abstract

Exposure to bacterial superantigens, such as staphylococcal enterotoxin B (SEB), can lead to the induction of acute lung injury/acute respiratory distress syndrome (ALI/ARDS). To date, there are no known effective treatments for SEB-induced inflammation. In the current study we investigated the potential use of the hyaluronic acid synthase inhibitor 4-methylumbelliferone (4-MU) on staphylococcal enterotoxin B (SEB) induced acute lung inflammation. Culturing SEB-activated immune cells with 4-MU led to reduced proliferation, reduced cytokine production as well as an increase in apoptosis when compared to untreated cells. Treatment of mice with 4-MU led to protection from SEB-induced lung injury. Specifically, 4-MU treatment led to a reduction in SEB-induced HA levels, reduction in lung permeability, and reduced pro-inflammatory cytokine production. Taken together, these results suggest that use of 4-MU to target hyaluronic acid production may be an effective treatment for the inflammatory response following exposure to SEB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / drug therapy
  • Acute Lung Injury / immunology
  • Animals
  • Anti-Inflammatory Agents / therapeutic use*
  • Apoptosis / drug effects
  • Capillary Permeability / drug effects
  • Cell Proliferation
  • Cytokines / immunology
  • Enterotoxins*
  • Glucuronosyltransferase / antagonists & inhibitors*
  • Hyaluronan Synthases
  • Hyaluronic Acid / immunology*
  • Hymecromone / therapeutic use*
  • Leukocytes / cytology
  • Leukocytes / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Pneumonia / drug therapy*
  • Pneumonia / immunology
  • T-Lymphocytes / drug effects

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Enterotoxins
  • enterotoxin B, staphylococcal
  • Hymecromone
  • Hyaluronic Acid
  • Glucuronosyltransferase
  • Hyaluronan Synthases