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The effect of bortezomib on expression of inflammatory cytokines and survival in a murine sepsis model induced by cecal ligation and puncture

Authors
 Sang Hoon Han  ;  Jin Seok Kim  ;  Jun Hee Woo  ;  Su Jin Jeong  ;  Jeon-Soo Shin  ;  Young Soo Ahn  ;  June Myung Kim 
Citation
 Yonsei Medical Journal, Vol.56(1) : 112-123, 2015 
Journal Title
 Yonsei Medical Journal 
ISSN
 0513-5796 
Issue Date
2015
MeSH
Animals ; Boronic Acids/administration & dosage ; Boronic Acids/pharmacology ; Boronic Acids/therapeutic use* ; Bortezomib ; Cecum/pathology* ; Cell Adhesion Molecules/metabolism ; Cell Line ; Cell Proliferation/drug effects ; Cell Survival/drug effects ; Chymotrypsin/metabolism ; Cytokines/metabolism* ; Disease Models, Animal ; Inflammation Mediators/metabolism* ; Ligation ; Lipopolysaccharides/pharmacology ; Lung/drug effects ; Lung/metabolism ; Lung/pathology ; Male ; Mice, Inbred C57BL ; Nitric Oxide/metabolism ; Proteasome Inhibitors/pharmacology ; Punctures ; Pyrazines/administration & dosage ; Pyrazines/pharmacology ; Pyrazines/therapeutic use* ; Sepsis/drug therapy*
Keywords
Bortezomib ; cecal ligation and puncture ; inflammatory cytokines ; lipopolysaccharide ; proteasome inhibitor
Abstract
PURPOSE: Although the proteasome inhibitor known as bortezomib can modulate the inflammatory process through the nuclear factor-kappa B signaling pathway, the immunomodulatory effect of pre-incubated bortezomib has not been fully evaluated for inflammation by infectious agents. Therefore, we evaluated the effect of bortezomib on the expression of inflammatory cytokines and mediators in macrophage cell lines and on survival in a murine peritonitis sepsis model. MATERIALS AND METHODS: Bortezomib was applied 1 hr before lipopolysaccharide (LPS) stimulation in RAW 264.7 cells. The cecal ligation and puncture (CLP) experiments were performed in C57BL/6J mice. RESULTS: Pre-incubation with bortezomib (25 nM or 50 nM) prior to LPS (50 ng/mL or 100 ng/mL) stimulation significantly recovered the number of viable RAW 264.7 cells compared to those samples without pre-incubation. Bortezomib decreased various inflammatory cytokines as well as nitric oxide production in LPS-stimulated cells. The 7-day survival rate in mice that had received bortezomib at 0.01 mg/kg concentration 1 hr prior to CLP was significantly higher than in the mice that had only received a normal saline solution of 1 mL 1 hr prior to CLP. In addition, the administration of bortezomib at 0.01 mg/kg concentration 1 hr before CLP resulted in a significant decrease in inflammation of the lung parenchyma. Collectively, pretreatment with bortezomib showed an increase in the survival rate and changes in the levels of inflammatory mediators. CONCLUSION: These results support the possibility of pretreatment with bortezomib as a new therapeutic target for the treatment of overwhelming inflammation, which is a characteristic of severe sepsis.
Files in This Item:
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DOI
10.3349/ymj.2015.56.1.112
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, June Myung(김준명)
Kim, Jin Seok(김진석) ORCID logo https://orcid.org/0000-0001-8986-8436
Shin, Jeon Soo(신전수) ORCID logo https://orcid.org/0000-0002-8294-3234
Ahn, Young Soo(안영수)
Jeong, Su Jin(정수진) ORCID logo https://orcid.org/0000-0003-4025-4542
Han, Sang Hoon(한상훈) ORCID logo https://orcid.org/0000-0002-4278-5198
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/139340
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