Modulation of nuclear factor-kappaB improves cardiac dysfunction associated with cardiopulmonary bypass and deep hypothermic circulatory arrest

被引:22
作者
Duffy, Jodie Y. [1 ,2 ,3 ,4 ]
McLean, Kelly M. [1 ,2 ]
Lyons, Jefferson M. [1 ,2 ]
Czaikowski, Adam J. [1 ,2 ]
Wagner, Connie J. [1 ,2 ]
Pearl, Jeffrey M. [5 ]
机构
[1] Cincinnati Childrens Hosp, Med Ctr, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Coll Med, Div Cardiothorac Surg, Cincinnati, OH USA
[3] Phoenix Childrens Hosp, Dept Surg, Phoenix, AZ USA
[4] Phoenix Childrens Hosp, Dept Pediat, Phoenix, AZ USA
[5] Phoenix Childrens Hosp, Dept Cardiothorac Surg, Phoenix, AZ USA
关键词
nuclear factor-kappaB; ischemia; reperfusion injury; cardiopulmonary bypass; calpain; troponin I; TROPONIN-I; B-ALPHA; PULMONARY-HYPERTENSION; TYROSINE PHOSPHORYLATION; CALPAIN; REPERFUSION; DEGRADATION; CALPASTATIN; INHIBITION; ACTIVATION;
D O I
10.1097/CCM.0b013e318194ab65
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: The hypothesis is that partial nuclear factor-kappaB (NF-kappa B) inhibition can alleviate cardiopulmonary dysfunction associated with ischemia and reperfusion injury following cardiopulmonary bypass and deep hypothermic circulatory arrest (CPB/DHCA) in a pediatric model. Design. Animal case study. Subjects: Two-week-old piglets (5-7 kg). Interventions. Piglets received 100 mu g/kg of SN50, a peptide inhibitor of NF-kappa B translocation and activation, 1 hour before CPB. The control group received saline. Animals were cooled to 18 degrees C with CPB, the piglets were in DHCA for 120 minutes, and the piglets were then rewarmed on CPB to 38 degrees C and maintained for 120 minutes after CPB/DHCA. Measurements: Sonomicrometry and pressure catheters collected hemodynamic data. Transmural left and right ventricular tissues were obtained at the terminal time point for determination of NF-kappa B activity by enzyme-linked immunosorbent assay. Data are expressed as mean +/- so. Main Points: Oxygen delivery was maintained at 76 +/- 13 mL/min at baseline and 75 +/- 5 mL/min at 120 minutes after CPB/DHCA (p = 0.75) in SN50-treated animals vs. 99 +/- 26 mL/min at baseline and 63 +/- 20 mL/min at 120 minutes in the untreated group (p = 0.0001). Pulmonary vascular resistance (dynes.sec(-1).cm(-5)) increased from 124 +/- 59 at baseline to 369 +/- 104 at 120 minutes in the untreated piglets (p = 0.001) compared with SN50-treated animals (100 24 at baseline and 169 88 at 120 minutes, p = 0.1). NF-kappa B activity was reduced by 74% in left ventricles of SN50-treated compared with SN50-untreated animals (p < 0.001). Plasma endothelin-1 (pg/mL), an important vasoconstrictor regulated by NF-kappa B, increased from 2.1 +/- 0.4 to 14.2 +/- 5.7 in untreated animals (p = 0.004) but was elevated to only 4.5 +/- 2 with SN50 treatment (p = 0.005). Conclusions. Improvement of cardiopulmonary function after ischemia/reperfusion was associated with the reduction of NF-kappa B activity in piglet hearts. Maintenance of systemic oxygen delivery and alleviation of pulmonary hypertension after CPB/DHCA in piglets administered SN50, possibly through a reduction of circulating endothelin-1, suggest that selective inhibition of NF-kappa B activity may reduce ischemia and reperfusion injury after pediatric cardiac surgery. (Crit Care Med 2009; 37:577-583)
引用
收藏
页码:577 / 583
页数:7
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