Cited 0 times in
Pretreatment with interleukin-6 small interfering RNA can improve the survival rate of polymicrobial cecal ligation and puncture mice by down regulating interleukin-6 production
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Mostafa Anower, AK | - |
dc.contributor.author | Shim, JA | - |
dc.contributor.author | Choi, B | - |
dc.contributor.author | Sohn, S | - |
dc.date.accessioned | 2013-04-24T06:18:07Z | - |
dc.date.available | 2013-04-24T06:18:07Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 0014-2999 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/7938 | - |
dc.description.abstract | Interleukin-6 (IL-6) is considered to be an early marker of severe sepsis that is associated with increased morbidity and mortality. Therefore, we pretreated male ICR mice with IL-6 small interfering RNA (siRNA) before cecal ligation and puncture (CLP) and observed the changes in their survival in response to down regulation of IL-6, as well as the role of Th subsets during sepsis. In addition, sham and CLP operated mice were sacrificed at different time points to determine the serum IL-6 levels during early and late sepsis. IL-6 siRNA pretreated septic mice showed markedly extended survival (23.3%) up to 10 days and significantly reduced serum IL-6 levels at day 5 (209.90 ± 0.50 pg/ml; P<0.0001) when compared to CLP mice at day 1. Furthermore, IL-6 mRNA and protein were highly expressed during early sepsis in CLP mice at day 1 and mRNA was not detected in IL-6 siRNA treated CLP mice at days 1 or 5 and serum level of IL-6 was also decreased significantly (P<0.01). In addition, the mRNA expression of C5aR, ROR-γt, PU.1 and protein expression of IL-17 were high at day 5 in IL-6 siRNA treated mice. Taken together, the results of the present study demonstrate that pretreatment with IL-6 siRNA improved CLP induced septic mice survival. Furthermore, the IL-6 level was down-regulated and the transcription factors ROR-γt and PU.1 were up-regulated by IL-6 siRNA at late sepsis. The results presented herein also suggest that IL-6 siRNA could be a potential molecular therapeutic strategy for the treatment of sepsis. | - |
dc.language.iso | en | - |
dc.subject.MESH | Alanine Transaminase | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Anti-Bacterial Agents | - |
dc.subject.MESH | Blood Urea Nitrogen | - |
dc.subject.MESH | Cecum | - |
dc.subject.MESH | Down-Regulation | - |
dc.subject.MESH | Interleukin-6 | - |
dc.subject.MESH | Ligation | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Mice, Inbred ICR | - |
dc.subject.MESH | Punctures | - |
dc.subject.MESH | RNA, Small Interfering | - |
dc.subject.MESH | Receptors, Complement | - |
dc.subject.MESH | Sepsis | - |
dc.subject.MESH | Survival Analysis | - |
dc.subject.MESH | Survival Rate | - |
dc.subject.MESH | T-Lymphocytes, Helper-Inducer | - |
dc.subject.MESH | Time Factors | - |
dc.title | Pretreatment with interleukin-6 small interfering RNA can improve the survival rate of polymicrobial cecal ligation and puncture mice by down regulating interleukin-6 production | - |
dc.type | Article | - |
dc.identifier.pmid | 22634167 | - |
dc.identifier.url | http://linkinghub.elsevier.com/retrieve/pii/S0014-2999(12)00434-7 | - |
dc.contributor.affiliatedAuthor | 손, 성향 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1016/j.ejphar.2012.05.007 | - |
dc.citation.title | European journal of pharmacology | - |
dc.citation.volume | 688 | - |
dc.citation.number | 1-3 | - |
dc.citation.date | 2012 | - |
dc.citation.startPage | 76 | - |
dc.citation.endPage | 83 | - |
dc.identifier.bibliographicCitation | European journal of pharmacology, 688(1-3). : 76-83, 2012 | - |
dc.identifier.eissn | 1879-0712 | - |
dc.relation.journalid | J000142999 | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.