Bristol Heart Institute, School of Clinical Science, University of Bristol, Bristol, United Kingdom.
Physiol Genomics. 2012 Nov 15;44(22):1098-106. doi: 10.1152/physiolgenomics.00072.2012. Epub 2012 Sep 18.
In cyanotic patients undergoing repair of heart defects, high level of oxygen during cardiopulmonary bypass (CPB) leads to greater susceptibility to myocardial ischemia and reoxygenation injury. This study investigates the effects of controlled reoxygenation CPB on gene expression changes in cyanotic hearts of patients undergoing surgical correction of tetralogy of Fallot (TOF). We randomized 49 cyanotic TOF patients undergoing corrective cardiac surgery to receive either controlled reoxygenation or hyperoxic/standard CPB. Ventricular myocardium biopsies were obtained immediately after starting and before discontinuing CPB. Microarray analyses were performed on samples, and array results validated with real-time PCR. Gene expression profiles before and after hyperoxic/standard CPB revealed 35 differentially expressed genes with three upregulated and 32 downregulated. Upregulated genes included two E3 Ubiquitin ligases. The products of downregulated genes included intracellular signaling kinases, metabolic process proteins, and transport factors. In contrast, gene expression profiles before and after controlled reoxygenation CPB revealed only 11 differentially expressed genes with 10 upregulated including extracellular matrix proteins, transport factors, and one downregulated. The comparison of gene expression following hyperoxic/standard vs. controlled reoxygenation CPB revealed 59 differentially expressed genes, with six upregulated and 53 downregulated. Upregulated genes included PDE1A, MOSC1, and CRIP3. Downregulated genes functionally clustered into four major classes: extracellular matrix/cell adhesion, transcription, transport, and cellular metabolic process. This study provides direct evidence that hyperoxic CPB decreases the adaptation and remodeling capacity in cyanotic patients undergoing TOF repair. This simple CPB strategy of controlled reoxygenation reduced the number of genes whose expression was altered following hyperoxic/standard CPB.
在接受心脏缺陷修复手术的发绀患者中,体外循环(CPB)期间高氧水平会导致心肌更容易发生缺血和再氧化损伤。本研究调查了控制性复氧 CPB 对接受法洛四联症(TOF)手术矫正的发绀患者心脏基因表达变化的影响。我们将 49 例接受矫正性心脏手术的发绀 TOF 患者随机分为接受控制性复氧或高氧/标准 CPB 组。在开始 CPB 和停止 CPB 前立即从心室心肌活检。对样本进行微阵列分析,并通过实时 PCR 验证阵列结果。高氧/标准 CPB 前后的基因表达谱显示 35 个差异表达基因,其中 3 个上调和 32 个下调。上调基因包括两个 E3 泛素连接酶。下调基因的产物包括细胞内信号转导激酶、代谢过程蛋白和转运因子。相比之下,控制性复氧 CPB 前后的基因表达谱仅显示 11 个差异表达基因,其中 10 个上调,包括细胞外基质蛋白、转运因子和一个下调。高氧/标准与控制性复氧 CPB 后基因表达的比较显示 59 个差异表达基因,其中 6 个上调和 53 个下调。上调基因包括 PDE1A、MOSC1 和 CRIP3。下调基因功能聚类为四个主要类别:细胞外基质/细胞黏附、转录、运输和细胞代谢过程。本研究提供了直接证据,表明高氧 CPB 降低了接受 TOF 修复的发绀患者的适应和重塑能力。这种简单的 CPB 复氧策略减少了高氧/标准 CPB 后基因表达改变的数量。