期刊文献+

肺保护性通气对急性呼吸窘迫综合征家兔肺外器官炎症反应的影响 被引量:7

Effects of protective ventilation on inflammatory response of extrapulmonary organs in acute respiratory distress syndrome rabbits
原文传递
导出
摘要 目的 研究肺保护性通气对急性呼吸窘迫综合征 (ARDS)肺外器官炎症反应的影响。方法 用生理盐水肺泡灌洗法复制ARDS家兔模型 ,分为 6组 (1)正常对照组 ;(2 )ARDS模型组 (ARDS) ;(3)小潮气量 (VT) +最佳呼气末正压 (PEEP)组 (LVBP) ;(4)常规VT+最佳PEEP组 (NVBP) ;(5 )小VT+高PEEP组 (LVHP) ;(6 )高VT+零PEEP组 (HVZP)。后 4组机械通气 4h后 ,用逆转录PCR法 (RT PCR)检测动物肝肠组织肿瘤坏死因子 (TNF)α和白介素 (IL) 10mRNA表达 ,酶联免疫吸附法 (ELISA)测定肝肠组织TNF α及IL 10浓度。结果 LVBP组肝组织TNF α和IL 10mRNA表达分别为 (42± 9)和 (2 5±10 ) ,与ARDS模型组相比较 ,差异无显著性 ,分别为 [(37± 7)和 (2 5± 4 ) ],但显著低于NVBP [分别(5 6± 7)和 (36± 8) ]、LVHP [(5 3± 10 )和 (35± 5 ) ]和HVZP组 [(70± 10 )和 (46± 5 ) ]。LVHP组TNF α和IL 10mRNA表达明显高于LVBP组 ,但明显低于HVZP组。LVBP组肝组织TNF α和IL 10浓度与ARDS组无明显差异 ,但显著低于NVBP、LVHP和HVZP组。HVZP组肝组织TNF α和IL 10浓度最高 ,不但高于LVBP组 ,也高于LVHP组。LVBP组的肠组织的TNF αmRNA表达为 (38± 11) ,与ARDS组比较无显著差异 ,但显著低于NVBP (5 1± 9)、LVHP (5 0± 11) Objective To evaluate the influence of protective ventilation on the inflammatory response of extrapulmonary organs in acute respiratory distress syndrome (ARDS) rabbits.Methods The ARDS rabbit model was established by saline alveolar lavage. The rabbits were divided into six groups: (1)normal;(2) ARDS group;(3) low-volume (V T) with best end-expiratory pressure (PEEP) (LVBP);(4)normal-volume(V T) with best PEEP (NVBP); (5) low-volume with high PEEP (LVHP)(6) high-volume zero PEEP (HVZP); Tumor necrosis factor (TNF)-α and interleukin (IL)-10 levels in liver and intestine homogenates were measured by ELISA and their mRNA expression RT-PCR.Results In the LVBP group, the TNF-α mRNA expression in liver was(42±9), which was lower than NVBP (56±7), LVHP (53+10), and HVZP group (70±10). But there was no different between LVBP and ARDS groups. TNF-α mRNA expression in LVHP group was higher than LVBP group in liver tissue, but lower than HVZP group significantly.Compared with LVBP group (25±9), the IL-10 mRNA expression increased significantly in NVBP (36±8), LVHP (35±5), and HVZP group (46 ± 5). Compared with LVBP group, the TNF-αand IL-10 concentrations in liver were increased markedly in NVBP, LVHP, and HVZP. But there was no difference between LVBP and ARDS group in TNF-α and IL-10 concentration in liver. Live TNF-α and IL-10 concentration was highest in HVZP group, which was higher than LVBP and LVHP group. In the LVBP group, the TNF-α mRNA expression in intestine was (38±11), which was lower than NVBP(51±9), LVHP (50±11), and HVZP group (64±11). But there was no different between LVBP and ARDS groups. The intestine TNF-α mRNA expression in LVHP group was higher than LVBP group, but lower than HVZP group significantly. As compared with LVBP group, the TNF-α concentration of intestine in NVBP, LVHP, and HVZP were markedly increased. But there was no difference between LVBP and ARDS group in TNF-α concentration of intestine. TNF-α concentration in intestine tissue was highest in HVZP group. As compared with LVBP group (22±7), the IL-10 mRNA expression in intestine increased significantly in NVBP(32 ± 7), LVHP(32 ± 8), and HVZP group (41± 5). IL-10 concentration of liver tissue in LVBP group showed no difference compared with ARDS group, but increased significantly in NVBP, LVHP, and HVZP group. IL-10 concentration in intestine tissue was highest in HVZP groups. The concentration of MPO and MDA showed no difference between ARDS and LVBP group. But compared with LVBP groups, the concentration of MPO and MDA increased significantly in NVBP, LVHP, and HVZP group.Conclusion Protective ventilation strategy can down-regulate inflammator mediator expression in the liver and intestine of ARDS rabbits and may prevent the occurrence of multiple organ dysfunction syndrome.
出处 《中华急诊医学杂志》 CAS CSCD 2004年第12期804-807,i001,共5页 Chinese Journal of Emergency Medicine
基金 江苏省医学重点基金 (H2 0 0 110 2 ) 江苏省 13 5医学重点人才基金 江苏省社会发展基金(BS2 0 0 0 40 9 BS990 3 2 )
关键词 ARDS TNF-α IL-10 肠组织 mRNA表达 PEEP 肺保护性通气 浓度 器官 家兔 Acute respiratory distress syndrome Inflammation response Protective ventilation strategy Multiple organ dysfunction syndrome
  • 相关文献

参考文献6

  • 1Parker JC, Hermandez LA, Peevy KJ. Mechanisms of ventilator-induced lung injury. Crit Care Med, 1993, 21:131-143.
  • 2Ranieri VM, Giunta F, Suter PM, et al. Mechanical ventilation as a mediator of multisystem organ failure in acute respiratory distress syndrome. JAMA, 2000, 284: 43-44.
  • 3韩扣兰,邱海波,谭焰,郭凤梅,周韶霞.控制性肺膨胀对急性呼吸窘迫综合征家兔血流动力学和气体交换的影响[J].徐州医学院学报,2002,22(3):189-192. 被引量:4
  • 4Imai Y, Parodo JB, Kajikawa O, et al. Injurious mechanical ventilation and end-organ epitheial cell apotosis and organ dysfunction in an experimental model of acute respiratory distress syndrome. JAMA, 2003,289: 2104-2112.
  • 5Haitsma JJ, Uhlig S, Goggel R, et al. Ventilator-induced lung injury leads to loss of alveolar and systemic compartmentalization of tumor necrosis factor-alpha. Intensive Care Med, 2000, 26: 1515-1522.
  • 6Guery BP, Welsh DA, Viget NB, et al. Ventilation-induced lung injury is associated with an increase in gut permeability. Shock, 2003, 19: 559-563.

二级参考文献7

  • 1[1]Rimensberger PC, Pristine G, Mullen BM, et al. Lung recruitment during small tidal volume ventilation allows minimal positive end - expiratory pressure without augmenting lung injury[J]. Crit Care Med,1999, 27(9): 1940 - 1945.
  • 2[2]Rimensberger PC, Pache JC, McKerlie C, et al. Lung recruitment and lung volume maintenance: a strategy for improving oxygenation and preventing lung injury during both conventional mechanical and highfrequency oscillation[J]. Intensive Care Med, 2000, 26(6):745 -755.
  • 3[3]Walsh MC,Carlo WA.Sustained inflation during HFOV improves pulmonary mechanics and oxygenation[J].J Appl Physiol,1988,65(1):368-372.
  • 4[4]Sohma A,Brampton WJ,Dunnill MS,et al.Effect of ventilation with positive end-expiratory pressure on the development of lung damage in experimental acid aspiration pneumonia in the rabbit[J].Intensive Care Med,1992,18(2):112-117.
  • 5[5]Smith KM,Mrozek JD,Simonton SC,et al.Prolonged partial liquid ventilation using conventional and high-frequency ventilators techniques:gas exchange and lung pathology in an animal model of of respiratiry distress syndrome[J].Crit Care Med,1997,25(11):1888-1897.
  • 6[6]Pelosi P,Cadringher P,Bottino N,et al.Sigh in acute respiratory distress syndrome[J].Am J Respir Crit Care Med,1999,159(3):872-880.
  • 7[7]Bon dDM,McAIoon J,FroeseAB.Sustained inflations improve respiratory compliance during high-frequency oscillatory ventilation but not dhning large tidal volume positive-pressure ventilation in rabbits[J].Crit Care Med,1994,22(8):1269-1277.

共引文献3

同被引文献65

引证文献7

二级引证文献21

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部