The ameliorative effects of a hypnotic bromvalerylurea in sepsis

Biochem Biophys Res Commun. 2015 Apr 3;459(2):319-326. doi: 10.1016/j.bbrc.2015.02.111. Epub 2015 Feb 28.

Abstract

Sepsis is a severe pathologic event, frequently causing death in critically ill patients. However, there are no approved drugs to treat sepsis, despite clinical trials of many agents that have distinct targets. Therefore, a novel effective treatment should be developed based on the pathogenesis of sepsis. We recently observed that an old hypnotic drug, bromvalerylurea (BU) suppressed expression of many kinds of pro- and anti-inflammatory mediators in LPS- or interferon-γ activated alveolar and peritoneal macrophages (AMs and PMs). Taken the anti-inflammatory effects of BU on macrophages, we challenged it to septic rats that had been subjected to cecum-ligation and puncture (CLP). BU was subcutaneously administered to septic rats twice per day. Seven days after CLP treatment, 85% of septic rats administrated vehicle had died, whereas administration of BU reduce the rate to 50%. Septic rats showed symptoms of multi-organ failure; respiratory, circulatory and renal system failures as revealed by histopathological analyses, blood gas test and others. BU ameliorated these symptoms. BU also prevented elevated serum-IL-6 level as well as IL-6 mRNA expression in septic rats. Collectively, BU might be a novel agent to ameliorate sepsis by preventing the onset of MOF.

Keywords: Inflammation; LPS; Macrophage; STAT transcription factor; TLR4.

MeSH terms

  • Animals
  • Bromisovalum / therapeutic use*
  • Cytokines / genetics
  • Cytokines / metabolism
  • Disease Models, Animal
  • Humans
  • Hypnotics and Sedatives / therapeutic use*
  • I-kappa B Proteins / metabolism
  • Interferon-gamma / metabolism
  • Interleukin-6 / blood
  • Interleukin-6 / genetics
  • Lipopolysaccharides / toxicity
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Male
  • Multiple Organ Failure / pathology
  • Multiple Organ Failure / physiopathology
  • Multiple Organ Failure / prevention & control
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • STAT1 Transcription Factor / metabolism
  • Sepsis / drug therapy*
  • Sepsis / etiology
  • Sepsis / physiopathology

Substances

  • Cytokines
  • Hypnotics and Sedatives
  • I-kappa B Proteins
  • Interleukin-6
  • Lipopolysaccharides
  • RNA, Messenger
  • STAT1 Transcription Factor
  • Stat1 protein, rat
  • Bromisovalum
  • Interferon-gamma