Effects of hypnotic bromovalerylurea on microglial BV2 cells

  • J Pharmacol Sci. 2017 Jun;134(2):116-123. doi: 10.1016/j.jphs.2017.05.007.
Shun Kawasaki  1 Naoki Abe  1 Fumito Ohtake  2 Afsana Islam  2 Mohammed Emamussalehin Choudhury  2 Ryo Utsunomiya  2 Satoshi Kikuchi  3 Tasuku Nishihara  4 Jun Kuwabara  5 Hajime Yano  2 Yuji Watanabe  5 Mayuki Aibiki  3 Toshihiro Yorozuya  4 Junya Tanaka  6
Affiliations
  • 1. Department of Molecular and Cellular Physiology, Graduate School of Medicine, Ehime University, Toon, Ehime 791-0295, Japan; Department of Anesthesiology and Resuscitology, Graduate School of Medicine, Ehime University, Toon, Ehime, Japan.
  • 2. Department of Molecular and Cellular Physiology, Graduate School of Medicine, Ehime University, Toon, Ehime 791-0295, Japan.
  • 3. Department of Emergency Medicine, Graduate School of Medicine, Ehime University, Toon, Ehime, Japan.
  • 4. Department of Anesthesiology and Resuscitology, Graduate School of Medicine, Ehime University, Toon, Ehime, Japan.
  • 5. Department of Gastrointestinal Surgery and Surgical Oncology, Graduate School of Medicine, Ehime University, Toon, Ehime, Japan.
  • 6. Department of Molecular and Cellular Physiology, Graduate School of Medicine, Ehime University, Toon, Ehime 791-0295, Japan. Electronic address: [email protected].
Abstract

An old sedative and hypnotic bromovalerylurea (BU) has anti-inflammatory effects. BU suppressed nitric oxide (NO) release and proinflammatory cytokine expression by lipopolysaccharide (LPS)-treated BV2 cells, a murine microglial cell line. However, BU did not inhibit LPS-induced nuclear translocation of nuclear factor-κB and subsequent transcription. BU suppressed LPS-induced phosphorylation of signal transducer and activator of transcription 1 (STAT1) and expression of interferon regulatory factor 1 (IRF1). The Janus kinase 1 (JAK1) inhibitor filgotinib suppressed the NO release much more weakly than that of BU, although filgotinib almost completely prevented LPS-induced STAT1 phosphorylation. Knockdown of JAK1, STAT1, or IRF1 did not affect the suppressive effects of BU on LPS-induced NO release by BV2 cells. A combination of BU and filgotinib synergistically suppressed the NO release. The mitochondrial complex I inhibitor rotenone, which did not prevent STAT1 phosphorylation or IRF1 expression, suppressed proinflammatory mediator expression less significantly than BU. BU and rotenone reduced intracellular ATP (iATP) levels to a similar extent. A combination of rotenone and filgotinib suppressed NO release by LPS-treated BV2 cells as strongly as BU. These results suggest that anti-inflammatory actions of BU may be attributable to the synergism of inhibition of JAK1/STAT1-dependent pathways and reduction in iATP level.

Keywords
ATP; Macrophage; Microglia; NO; Rotenone.
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