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氯胺酮对盲肠结扎穿孔(CLP)诱导的脓毒症大鼠肠道中细胞因子、核因子κB(NF-κB)和Toll样受体(TLRs)水平的影响。

Effects of ketamine on levels of cytokines, NF-kappaB and TLRs in rat intestine during CLP-induced sepsis.

作者信息

Yu Min, Shao Danbing, Liu Jian, Zhu Juan, Zhang Zhijie, Xu Jianguo

机构信息

Department of Anesthesiology, Jinling Hospital, School of Medicine, Nanjing University, 305 East Zhongshan Road, Nanjing 210002, PR China.

出版信息

Int Immunopharmacol. 2007 Aug;7(8):1076-82. doi: 10.1016/j.intimp.2007.04.003. Epub 2007 May 2.

Abstract

This study was designed to investigate the effects of ketamine on levels of inflammatory cytokines, nuclear factor-kappa B (NF-kappaB) and Toll-like receptors (TLRs) in rat intestine during polymicrobial sepsis, induced by cecal ligation and puncture (CLP). After the induction of sepsis or sham-operation, the rats were treated with ketamine (2.5, 5 or 10 mg/kg) or saline (10 ml/kg). At 2, 4 or 6 h post-operation, the intestinal concentrations of inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha) and interleukin (IL)-6, were determined by enzyme-linked immunosorbent assay (ELISA). Activity of NF-kappaB in rat intestine was assessed by electrophoretic mobility shift assay (EMSA). And expressions of Toll-like receptor 2 (TLR2) and Toll-like receptor 4 (TLR4) of rat intestine were examined by reverse transcription-polymerase chain reaction (RT-PCR). We found that TNF-alpha and IL-6 concentrations, NF-kappaB activity, TLR2 and TLR4 expressions in rat intestine were increased after CLP. At the doses of 5 and 10 mg/kg, ketamine suppressed CLP-induced elevation of IL-6. Ketamine 2.5, 5 and 10 mg/kg after CLP decreased intestinal TNF-alpha level and NF-kappaB activity, and inhibited TLR2 and TLR4 expressions as well. These results suggest that ketamine may have anti-inflammatory effects, such as suppressing the levels of inflammatory cytokines and attenuating NF-kappaB activity, during polymicrobial sepsis. And these anti-inflammatory effects possibly correlate with the inhibitory influence of ketamine on TLR2 and TLR4 expressions.

摘要

本研究旨在探讨氯胺酮对盲肠结扎穿刺(CLP)诱导的大鼠多微生物脓毒症期间肠道炎症细胞因子、核因子-κB(NF-κB)和Toll样受体(TLRs)水平的影响。在诱导脓毒症或假手术后,大鼠接受氯胺酮(2.5、5或10mg/kg)或生理盐水(10ml/kg)治疗。术后2、4或6小时,通过酶联免疫吸附测定(ELISA)测定肠道炎症细胞因子如肿瘤坏死因子-α(TNF-α)和白细胞介素(IL)-6的浓度。通过电泳迁移率变动分析(EMSA)评估大鼠肠道中NF-κB的活性。并通过逆转录-聚合酶链反应(RT-PCR)检测大鼠肠道中Toll样受体2(TLR2)和Toll样受体4(TLR4)的表达。我们发现CLP后大鼠肠道中TNF-α和IL-6浓度、NF-κB活性、TLR2和TLR4表达增加。在5和10mg/kg剂量下,氯胺酮抑制CLP诱导的IL-6升高。CLP后2.5、5和10mg/kg氯胺酮降低肠道TNF-α水平和NF-κB活性,并抑制TLR2和TLR4表达。这些结果表明,氯胺酮在多微生物脓毒症期间可能具有抗炎作用,如抑制炎症细胞因子水平和减弱NF-κB活性。并且这些抗炎作用可能与氯胺酮对TLR2和TLR4表达的抑制作用相关。

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