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Humulone suppresses replication of respiratory syncytial virus and release of IL-8 and RANTES in normal human nasal epithelial cells
Authors:Jun Fuchimoto  Takashi Kojima  Tamaki Okabayashi  Tomoyuki Masaki  Noriko Ogasawara  Kazufumi Obata  Kazuaki Nomura  Satoshi Hirakawa  Naoyuki Kobayashi  Tatsuro Shigyo  Shin-ichi Yokota  Nobuhiro Fujii  Hiroyuki Tsutsumi  Tetsuo Himi  Norimasa Sawada
Affiliation:1. Frontier Laboratories of Value Creation, Sapporo Breweries Ltd, Shizuoka, 425-0013, Japan
2. Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060-8556, Japan
3. Research Institute for Microbial Diseases, Osaka University, Suita, 565-0871, Japan
4. Department of Otolaryngology, Sapporo Medical University School of Medicine, Sapporo, 060-8556, Japan
5. Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, 060-8556, Japan
6. Department of Microbiology, Sapporo Medical University School of Medicine, Sapporo, 060-8556, Japan
Abstract:Respiratory syncytial virus (RSV) is the major infectious agent causing serious respiratory tract inflammation in infants and young children. However, an effective vaccine and anti-viral therapy for RSV infection have not yet been developed. Hop-derived bitter acids have potent pharmacological effects on inflammation. Therefore, we investigated the effects of humulone, which is the main constituent of hop bitter acids, on the replication of RSV and release of the proinflammatory cytokine IL-8 and chemokine RANTES in RSV-infected human nasal epithelial cells (HNECs). We found that humulone prevented the expression of RSV/G-protein, formation of virus filaments and release of IL-8 and RANTES in a dose-dependent manner in RSV-infected HNECs. These findings suggest that humulone has protective effects against the replication of RSV, the virus assembly and the inflammatory responses in HNECs and that it is a useful biological product for the prevention and therapy for RSV infection.
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