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低温肺保护液肺动脉灌注在体外循环中的肺保护作用 被引量:6

Lung protection of pulmonary artery perfusion with hypothermic protective solution during cardiopulmonary bypass
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摘要 目的研究低温肺保护液在体外循环(CPB)心脏直视手术中对肺损伤的保护作用。方法选择30例重度肺动脉高压先心病患者,随机分为对照组和肺保护组,每组15例。肺保护组CPB术中一次性从肺动脉灌注低温肺保护液,对照组未行肺动脉灌注。分别于麻醉诱导前(T1),阻断升主动脉30min(T2),CPB结束后1h(T3)、24h(T4)、36h(T5)取桡动脉血标本动态检测两组患者各时间点的肿瘤坏死因子-α(TNF-α)、白细胞介素-10(IL-10);在T1、T3、T4、T5各时间点对比观察两组术后肺泡一动脉血氧分压差(A—aDO2)和呼吸指数(RI)。结果两组一般资料差异无统计学意义(P〉0.05);CPB开始后,两组桡动脉血TNF-α、IL-10进行性增高。TNF-α于CPB结束后1h达到最高[对照组(148.42±23.10)ng/L,保护组(103.29±32.15)ng/L],后逐渐下降,但仍高于CPB前,对照组增高更显著(P〈0.01)。IL-10于CPB结束后24h达到最高[对照组(66.75±25.82)ng/L,保护组(85.12±20.68)ng/L],后逐渐下降,但仍高于CPB前,肺保护组增高更显著(P〈0.05)。CPB开始后,两组A—aD02和RI进行性增加(A—aD02对照组195.8±72.5,保护组161.3±33.2;RI对照组0.72±0.05,保护组0.56±0.08);对照组T3、T4、T5的A—aDO2及RI明显高于肺保护组(P〈0.01)。结论CPB术后存在肺损伤,低温肺保护液可以抑制炎症因子TNF-α的产生,上调抗炎因子IL-10的释放,减轻肺损伤,改善术后肺功能。 Objective To investigate the protective effect of hypothermic protective solution on lungs in eardiopulmonary bypass(CPB ) patients. Methods 30 patients with congenital heart disease and severe pulmonary hypertension were divided into the control group(n= 15) and the protective group(n= 15). The patients in the control group were performed using routine techniques, and in the protective group patients pulmonary artery were infused with 4 ℃ protective solution during CPB. Blood samples were drawn from radial artery before induetion(T1), 30 min following clamping(T2), 1 h after CPB(T3), 24 h after CPB(T4) and 36 h after CPB(T5). Tumor necrosis factor-α(TNF-α),interleukin-10(IL-10) were measured by ELISA perioperatively in both group. Alveolar-arterial oxygen gradient A-aDO2 and Respiratory indexes (RI) were recorded at T1,T3,T4,Ts. Results There were no differences in the values of TNF-α, IL-10, A-aDo2 and RI at T1 (base value) between the two group. After CPB, the levels of TNF-α,IL-10 increased compared with the T1 in both group. The plasma levels of TNF-α in th protective group were significantly lower than the control group (P〈0.01). The plasma levels of IL-10 in the protective group were significantly higher than the control group (P〈0.05). Compared with the control group, protective group showed lower RI and lower A-aDO2 after operation(P〈0.01 ). Conclusion Lung injury exists after t he surgery by CPB. The hypothermic protective solution could significandy inhibit the inflammatory cytokine TNF-α release and significantly increase the anti-inflammatory eytokine IL-10 release, and could protect lungs during eardiopulmonary bypass.
出处 《中国心血管病研究》 CAS 2009年第3期198-201,共4页 Chinese Journal of Cardiovascular Research
关键词 低温肺保护液 体外循环 肺动脉灌注 肺保护 Hypothermia protective solution Cardiopulmonary bypass Pulmonary artery perfusion Lung protection
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  • 1任斌辉,景华,李德闽,李忠东.乌司他丁对肺功能的保护作用[J].医学研究生学报,2004,17(6):519-521. 被引量:20
  • 2王电军,刘建新,尹邦良.乌司他丁对体外循环肺损伤的保护作用[J].中南大学学报(医学版),2005,30(6):670-672. 被引量:7
  • 3[1]Killy RA,Smith TW.Cytokines and cardiac contractile function.Circulation,1997,95:778.
  • 4[3]Murry DR,Biohil M,Bies DA,et al.Basic mechanisms in congestive heart failure.Circ Res,1996,78:154.
  • 5[4]Kawamura T,Wakusawa R,Okada K.Evaluation of cytokines during open heart surgery with cardiopulmonary bypass:participation of IL-8 and IL-6 in reperfusion injury.Can J A naesth,1993,56(Suupl):S92-S96.
  • 6[1]HansenPR.Role of neutrophilsin myocardial ischemia and reperfusion.Circulation,1995,91:1872-1885.
  • 7[2]Eierman DF,Yagami M,Erme SM,et al.Endogenously opsonized particles divert prostanoidaction from lethaltoprotective in models of experimental endotoxemia.Proc Nail Acad Sci USA,1995,92:2815-2819.
  • 8[3]Minhaz L,Tanaka M,Tsukamate H,et al.Effec to fMU-186 on postischemic reperfusion injury in isolated rat heart.Free RadicRes,1996,24:361-367.
  • 9[4]Chen LY,Nichols WW,Hendricks J,et al.Myocardial neutrophilin fitration,lipid peroxidation,and anti-oxidant activity after coronary artery chrombosis and thrombolysis.Am Heart J,1995,129:211-218.
  • 10[5]Kahn NN.Platelet-stimulated thrombin and PUGF are normalized by insulinand Ca2+ chennel blockers.Am J physiol,1999,276:E856-862.

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