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体外循环期间应用右美托咪定对猪外周血单核细胞TLR-4,5/NF-κB信号通路的影响 被引量:3

Effect of dexmedetomidine on TLR-4,5/NF-κB signal pathway in swine peripheral blood mononuclear cells during cardiopulmonary bypass
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摘要 目的探讨右美托咪定对猪体外循环(CPB)期间外周血单核细胞TLR-4,5/NF-κB信号通路的影响。方法实验选择五指山小型猪20头,随机分为4组(n=5):右美托咪定组(D组),右美托咪定+育亨宾组(DY组),育亨宾组(Y组),对照组(C组)。D组和DY组在麻醉诱导前静脉输注右美托咪定1μg/kg,随后以0.5μg/(kg·h)速率维持至手术结束;DY组在静脉输注右美托咪定前给予育亨宾l mg/kg;Y组和C组在麻醉诱导前分别给予育亨宾1 mg/kg和等量生理盐水。在CPB前(T_0)、CPB后1(T_1)及2 h(T_2)、停CPB后1(T_3)及2 h(T_4),采集血标本检测外周血CD16^+单核细胞TLR4、5和NF-κB的阳性表达率,血浆中TNF-α浓度。结果与D组比较,C组和DY组在T_(1-4)时点外周血CD16^+单核细胞TLR4、5和NF-κB阳性表达率,血浆中TNF-α浓度均增高。结论右美托咪定通过兴奋α_2肾上腺素受体,抑制TLR-4,5/NF-κB信号通路的激活从而减轻体外循环诱发的全身炎症反应。 Objective To evaluate the effect of dexmedetomidine on TLR-4,5/NF-κB signal pathway in swine peripheral blood mononuclear cells during cardiopulmonary bypass(CPB).Methods Twenty swine were randomly divided into 4 groups(n=5 each):dexmedetomidine group(group D),dexmedetomidine+Yohimbine group(group DY),Yohimbine group(group Y),and control group(group C).In group D and group DY,1.0μg/kg bolus dose of dexmedetomidine were administered before the induction of anesthesia,followed by 0.5μg/(kg·h)infusion until the end of surgery;in group DY,1.0 mg/kg dose of Yohimbine was administered before infusing dex-medetomidine;in group Y,only 1.0 mg/kg dose of Yohimbine was administered before the induction of anesthe-sia,while in group C equal volume of normal saline was infused instead of dexmedetomidine.Blood samples were collected to detect the positive expression rate of toll-like receptor 4 and 5(TLR4,5)and nuclear factor KappaB(NF-κB)in peripheral blood CD16^+mononuclear cells before CPB(T0),1 h,2 h after CPB(T1-2)and 1 h,2 h after termination of CPB(T3-4),and so did the measurement of the concentrations of tumor necrosis factor-alpha(TNF-α),interleukin-6(IL-6),and interleukin-10(IL-10)in plasma.Result Compared to group D,the posi-tive expression rate of TLR4,5 and NF-κB in peripheral blood CD16^+mononuclear cells were significantly increased in group C and DY,the concentrations of TNF-α,IL-6 were significantly increased and the concentra-tions of IL-10 were significantly decreased in group C and group DY at 1 h,2 h after CPB(T1-2)and 1 h,2 h after termination of CPB(T3-4)(P≤0.05).Conclusion Dexmedetomidine can reduce inflammatory response in CPB.The mechanism is related to the inhibition of the activation of TLR-4,5/NF-κB signal pathway by excitedα2 adren-ergic receptors.
作者 罗琳 魏晓 陈梅珠 李美霞 LUO Lin;WEI Xiao;CHEN Meizhu;LI Meixia(Department of Anesthesiology,Haikou Municipal Hospital,Haikou 570208,China)
出处 《实用医学杂志》 CAS 北大核心 2018年第22期3774-3778,共5页 The Journal of Practical Medicine
基金 海南省自然科学基金(编号:2017817385).
关键词 右美托咪定 体外循环 TOLL样受体 核转录因子ΚB 育亨宾 dexmedetomidine cardiopulmonary bypass(CPB) Toll-like receptor NF-κB Yohimbine
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  • 1Dalakas Marinos C.Immunotherapy of myositis:issues,concerns andfuture prospects[J].Nat Rev Rheumatol,2010,6(3):129-137.
  • 2Allenbach Y,Solly S,Gre’goire S,et al.Role of regulatory T cells ina new mouse model of experimental autoimmune myositis[J].Am JPathol,2009,174(3):989-998.
  • 3Park BS,Song DH,Kim HM,et al.The structural basis of lipopo-lysaccharide recognition by the TLR4-MD-2 complex[J].Nature,2009,458(7242):1191-1195.
  • 4Meng J,Gong M,Bjrkbacka H,et al.Genome-wide expression pro-filing and mutagenesis studies reveal that lipopolysaccharide respon-siveness appears to be absolutely dependent on TLR and MD-2 expres-sion and is dependent upon intermolecular ionic interactions[J].J Im-munol,2011,187(7):3683-3693.
  • 5Richez C,Blanco P,Rifkin I,et al.Role for toll-like receptors in au-toimmune disease:the example of systemic lupus erythematosus[J].Joint Bone Spine,2011,78(2):124-130.
  • 6Summers SA,Hoi A,Steinmetz OM,et al.TLR9 and TLR4 are re-quired for the development of autoimmunity and lupus nephritis inpristane nephropathy[J].J Autoimmune,2010,35(4):291-298.
  • 7Shimamoto A,Chong AJ,Yada M,et al.Inhibition of Toll-like recep-tor 4 with eritoran attenuates myocardial ischemia-reperfusion injury[J].Circulation,2006,114(1 Suppl):1270-1274.
  • 8Dalakas Marinos C.Pathophysiology of inflammatory and autoimmunemyopathies[J].Presse Med,2011,40:e237-e247.
  • 9Yang QW, Wang JZ, Li JC, et al. High-mobility group protein box-1 and its relevance to celebral ischemia [J]. J Cereb Blood Flow Metab, 2010,30(2) : 243-254.
  • 10Evankovich J, Cho SW, Zhang R, et al. High mobility group Box 1 release from hepatocytes during ischemia and reperfusion injury is mediated by decreased histone deacetylase activity [J ]. J Biol Chem, 2010, 285 (51) : 39888-39897.

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