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可溶性白细胞分化抗原14和可溶性肿瘤坏死因子受体-P55治疗严重烫伤小鼠实验研究 被引量:6

Experimental Studies on the Therapic Effect of sCD14 and sTNFR-P55 on the Serious Scalded Mice
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摘要 目的:观察可溶性白细胞分化抗原14(sCD14)和可溶性肿瘤坏死因子受体-P55(sTNFR-P55)对严重烫伤模型小鼠炎症反应、胰岛素抵抗和胰岛素分泌的治疗效果。方法:模型小鼠单独及联合静脉注射sCD14和sTNFR-P55,观察不同治疗组以及治疗对照组(模型组)、正常对照组的死亡率、外周血白细胞(WBC)总数、稳态模式胰岛素抵抗(HOMA-IR)指数和胰岛素分泌(HOMA-β)指数以及空腹血糖和乳酸含量变化。结果:sCD14和sTNFR-P55联合组小鼠死亡率明显低于治疗对照组(P<0.05);联合组及单一治疗组WBC总数、HOMA-IR指数、空腹血糖和乳酸含量均明显低于治疗对照组,且联合组低于单一治疗组;但HOMA-β指数治疗组明显高于治疗对照组(P<0.01),且联合组高于单一治疗组(P<0.01)。结论:静脉注射sCD14和sTNFR-P55能够有效改善创伤炎症反应、胰岛素抵抗和胰岛β细胞功能障碍,降低创伤模型小鼠病死率,且联合治疗效果优于单一治疗。 OBJECTIVE: To study the therapic effect of soluble cluster of differentiation (sCD14) and soluble tumor necrosis factor receptor-P55(sTNFR-P55) on the inflammation,insulin resisitance and insulin secretion of serious scalded mice. METHODS: The lecels of mortality, peripheral white blood cell(WBC), Homeostasis Assessment-Insulin Resistance (HOMA-IR) and Homeostasis Assessmen- β(HOMA-β), fasting glucose, fasting lactic acid of the scalded mice treated individually by infusion with sCD14,sTNFR- P55,and both the sCD14 and sTNFR-P55, were examined compared with that of the control. RESULTS: The mortality of the scalded mice treated both by infusion with both of sCD14 and sTNFR-p55, were lower than that of the control(P 〈 0.05). The levels of WBC, HOMA - IR, HOMA- β, fasting glucose, fasting lactic acid of treated scalded mice were all lower than that of the control scalded mice(P〈0.01), and that of the scalded mice individually treated by sCD14 or sTNFR- p55 were lower than that of both treated by sCD14 and sTNFR-P55(P〈0.01). CONCLUSIONS: The treatment with sCD14 and sTNFR- P55 by mainline could contribute to ameliorate the inflammation, insulin resistance, disfunction of islet β cell, reduce the traumatic mortality. The therapic effect of treatment with both the sCD14 and sTNFR - P55 was better than that of treatment with single one.
出处 《中国药房》 CAS CSCD 北大核心 2007年第34期2653-2655,共3页 China Pharmacy
基金 南京军区医药卫生"十一五"资助重大课题(06Z25)
关键词 SCD14 sTNFR—P55 烫伤 胰岛素抵抗 胰岛口细胞功能不全 sCD14 sTNFR- P55 Scald Insulin resistance Disfunction of islet β cell
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  • 1江明性.药理学[M].北京:人民卫生出版社,1989,3.13-13.
  • 2周衍椒.生理学[M].北京:人民卫生出版社,1989.125.
  • 3Dellinger 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.
  • 4Tsai 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.
  • 5Das UN. Insulin and the critically ill. Crit Care, 2002, 6:262-263.
  • 6Hansen 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.
  • 7Yu 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.
  • 8Tschaikowsky 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.
  • 9van den Berghe G, Wouters P, Weekers F,et al. Intensive insulin therapy in critically ill. N Engl J Med, 2001, 345:1359-1367.
  • 10Netea MG, van der Meer JW, Kullberg BJ. Sepsis-theory and therapies. N Engl J Med, 2003, 348:1600-1602.

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