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胰岛素对脓毒症单核细胞分泌和抗原递呈功能的影响 被引量:7

Effects of insulin on monocytic cytokines production and expression of HLA-DR in human septics
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摘要 目的探讨不同胰岛素水平对脓毒症患者的体外单核细胞分泌和抗原递呈功能的影响。方法分离10例脓毒症(sepsis)患者外周血单核细胞进行体外培养。根据培养液中胰岛素浓度的不同分为5组:A组(不含胰岛素)、B组(胰岛素浓度为10μU/ml)、C组(100μU/ml)、D组 (1000μU/ml)和E组(5000μU/ml)。在不同培养液中培养24 h,观察单核细胞内毒素刺激后的分泌细胞因子(TNF-α、IL-6、IL-10)和抗原递呈功能(HLA-DR表达)的变化。结果单核细胞经过24 h 的培养,内毒素刺激后分泌TNF-α和IL-6的能力在较低胰岛素浓度时均无明显变化。当培养液中胰岛素浓度增加到1000μU/ml时,单核细胞分泌TNF-α和IL-6的能力均显著下降(A组与D组比较, P<0.05)。在各胰岛素浓度下,单核细胞分泌IL-10和表面抗原HLA-DR的表达均无明显变化。结论胰岛素能抑制内毒素刺激后脓毒症患者单核细胞分泌IL-6、TNF-α等炎性细胞因子的能力。提示外源性给予胰岛素对脓毒症患者有潜在的抗炎作用。 Objective To observe the in vitro cytokines production and expression of human leukocyte antigen DR (HLA-DR) in monocytes in human septics. Methods Monocytes were isolated from 10 septic patients to observe the secretion function of TNF-α, IL-6 and IL-10 and HLA-DR expression in monocytes. Monocytes were isolated and incubated with different concentration of insulin : group A ( no insulin), group B ( 10μU/ml) ,group C ( 100μU/ml) ,group D ( 1000 μU/ml) and group E (5000μU/ ml), for 24 hours at 37℃. The levels of TNF-α, IL-6 and IL-10 in the supernatants were tested by ELISA. The antigen presenting function represented by HLA-DR expression was detected by flow cytometry analysis. Results With lower insulin concentration of culture media, secretion of TNF-α and IL-6 did not change in monocytes after excitation by LPS. When the insulin concentration elevated to 1000μU/ml, monocyte excretion of TNF-α and IL-6 was on significant depression ( group D vs. group A, P 〈 0. 05). Along with upgraded insulin concentration in culture media, the expression of HLA-DR and the secretion of IL-10 in monocyte was not changed. Conclusion Insulin has the ability to suppress synthesis of TNF-α and IL-6 in monocytes in human sepsis, and hence benefits the treatment of sepsis and septic shock.
出处 《中华普通外科杂志》 CSCD 北大核心 2006年第3期218-220,共3页 Chinese Journal of General Surgery
基金 军队"十五"重点科研基金资助项目(01Z011)
关键词 脓毒症 单核细胞 胰岛素 Sepsis Monocytes Insulin
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参考文献8

  • 1Netea MG.Van der Meer JW.KuHberg BJ.Sepsis theory and therapies.N Engl J Med,2003,348:1600-1602.
  • 2虞文魁,李维勤,王晓东,燕晓雯,祁晓平,李宁,黎介寿.胰岛素严格控制血糖对脓毒症患者的影响及其机理的初步探讨[J].中华外科杂志,2005,43(1):29-32. 被引量:47
  • 3ACCP/SCCM Consensus Conference:Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis.Crit Care Med,1992,20:864-874.
  • 4Haupt W,Fritzsche H,Hohenberger W,et al.Selective cytokine release induced by serum and separated plasma from septic patients.Eur J Surg,1996,162:769-776.
  • 5Van den Berghe G,Wouters P,Weekers F,et al.Intensive insulin therapy in critically ill patients.N Engl J Med,2001,345:1359-1367.
  • 6Aljada A,Ghanim H,Saadesh R,et al.Insulin inhibits NFκB and MCP-1 expression in human aortic endothelial cells.J Clin Endocrinol Metab,2001,86:450-453.
  • 7Webb S.The role of mediators in sepsis resolution.Adv Sepsis,2002,2:8-14.
  • 8Das UN.Current advances in sepsis and septic shock with particular emphasis on the role of insulin.Med Sci Monit,2003,9:181-192.

二级参考文献9

  • 1Dellinger RP, Carlet JIM, Masur H, et al. Surviving Sepsis Campaign Management Guidelines Committee. Surviving sepsis campaign guidelines for management of severe sepsis and septic shock. Crit Care Med, 2004, 32:858-873.
  • 2Tsai MH, Peng YS, Lien JM, et al. Multiple organ system failure in critically Ill cirrhotic patients. A comparison of two multiple organ dysfunction/failure scoring systems. Digestion, 2004, 69:190-200.
  • 3Das UN. Insulin and the critically ill. Crit Care, 2002, 6:262-263.
  • 4Hansen TK, Thiel S, Wouters PJ, et al. Intensive insulin therapy exerts antiinflammatory effects in critically ill patients and counteracts the adverse effect of low mannose-binding lectin levels. J Clin Endocrinol Metab, 2003,88:1082-1088.
  • 5Yu WK, Li WQ, Li N, et al. Mononuclear histocompatibility leukocyte antigen-DR expression in the early phase of acute pancreatitis. Pancreatology, 2004, 27,4:233-243.
  • 6Tschaikowsky K, Hedwig-Geissing M, Schiele A, et al. Coincidence of pro- and anti-inflammatory responses in the early phase of severe sepsis: longitudinal study of mononuclear histocompathtibility leukocyte antigen-DR expression, procalctonin, C-reactive protein, and changes in T-cell subsets in septic and postoperative patients. Crit Care Med, 2002,30:1015-1023.
  • 7van den Berghe G, Wouters P, Weekers F,et al. Intensive insulin therapy in critically ill. N Engl J Med, 2001, 345:1359-1367.
  • 8Netea MG, van der Meer JW, Kullberg BJ. Sepsis-theory and therapies. N Engl J Med, 2003, 348:1600-1602.
  • 9American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference: definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis.Crit Care Med, 1992,20:864-874.

共引文献46

同被引文献40

  • 1虞文魁,李维勤,王晓东,燕晓雯,祁晓平,李宁,黎介寿.胰岛素严格控制血糖对脓毒症患者的影响及其机理的初步探讨[J].中华外科杂志,2005,43(1):29-32. 被引量:47
  • 2胡兴国,张云翔,曾因明.危重病人应激性高血糖的研究进展[J].国外医学(麻醉学与复苏分册),2005,26(3):140-143. 被引量:72
  • 3申传安,柴家科,姚咏明,杜晓辉,盛志勇.胰岛素强化治疗对烫伤脓毒症兔骨骼肌蛋白高降解的调节及其机制[J].中国危重病急救医学,2006,18(3):139-142. 被引量:12
  • 4Van den Berghe G,Wouters P,Weekers F,et al.Intensive insulin therapy in critically ill patients.N Engl J Med,2001,345:1359-1367.
  • 5Levy MM,Fink MP,Marshall JC,et al.2001 SCCM /ESICM /ACCP/ATS/SIS ternational-sepsis definitions conference.Crit Care Med,2003,31:1250-1256.
  • 6Esposito K,Nappo F,Marfell R,et al.Inflammatory cytokine concentrations are acutely increased by hyperglycemia in human:role of oxidative stress.Circulation,2002,106:2067-2072.
  • 7Marc G.Jeschke MD,Ph D,et al.Herndon,MD.Insulin treatment improves the systemic inflammatory reaction to severe trauma.Annals of Surgery,2004,239:553-560.
  • 8Wang XP, Wang BX, Wu JX, et al. Beneficial effects of growth hormone on bacterial translocation during the course of acute necrotizing pancreatitis in rats. Pancreas,2001,23 (2) : 148-156.
  • 9Yi C,Cao Y,Wang SR,et al. Beneficial effect of recombinant human growth hormone on the intestinal mucosa barrier of septic rats. Braz J Med Biol Res,2007,40( 1 ) :41-48.
  • 10Uronen HH, Allen ML, Lichtarowicz KE, et al. Growth hormone enhances proinflammatory cytokine production by monoeytes in whole blood. Growth Horm IGF Res,2003,13 (5) :282-286.

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