Seehase Matthias, Quentin Thomas, Wiludda Elke, Hellige Gerhard, Paul Thomas, Schiffmann Holger
Department of Pediatric Cardiology and Pediatric Intensive Care, Georg-August-Universitat, Gottingen, Germany.
Biol Neonate. 2006;90(3):174-84. doi: 10.1159/000092888. Epub 2006 Apr 25.
Neonatal hearts are less susceptible to developing myocardial dysfunction after hypoxia and/or ischemia than adult hearts. Differences in intracellular calcium homeostasis may be responsible for reduced calcium overload of the immature myocardium leading to the observed protection against ischemia.
To assess differences in baseline and post-ischemic gene expression of calcium handling proteins after ischemia in neonatal and adult rabbit hearts.
We used isolated antegrade perfused rabbit hearts (age 2 days, 28 days, n = 32), which were exposed to ischemia and hypothermia simulating myocardial stunning comparable to neonatal asphyxia. Gene and protein expression of the sodium-calcium exchanger (NCX), the sarco-endoplasmatic reticulum Ca2+-ATPase 2a (SERCA) and calsequestrin (CSQ) were measured using quantitative real-time PCR and Western blotting.
After ischemia and reperfusion in neonatal and adult hearts, a significant decrease in myocardial performance was recorded. At the mRNA level, significant differences in the baseline expression of NCX, SERCA and CSQ between neonatal and adult hearts were observed. In neonatal post-ischemic hearts, NCX and CSQ expression were significantly higher at the mRNA level than in controls. In contrast, SERCA expression remained unchanged in neonatal hearts and decreased in adult hearts compared to the non-ischemic controls.
These findings suggest that changes in gene expression of calcium handling proteins may be involved in the different susceptibility of neonatal compared to adult hearts to developing myocardial dysfunction after ischemia.
与成年心脏相比,新生儿心脏在缺氧和/或缺血后发生心肌功能障碍的可能性较小。细胞内钙稳态的差异可能是未成熟心肌钙超载减少的原因,从而导致观察到的对缺血的保护作用。
评估新生兔和成年兔心脏缺血后钙处理蛋白的基线和缺血后基因表达差异。
我们使用离体顺行灌注兔心脏(2日龄、28日龄,n = 32),使其暴露于模拟新生儿窒息的缺血和低温环境中,以引发心肌顿抑。使用定量实时PCR和蛋白质印迹法测量钠钙交换体(NCX)、肌浆网Ca2+-ATP酶2a(SERCA)和肌集钙蛋白(CSQ)的基因和蛋白质表达。
新生兔和成年兔心脏缺血再灌注后,心肌功能均显著下降。在mRNA水平上,观察到新生兔和成年兔心脏NCX、SERCA和CSQ的基线表达存在显著差异。在新生兔缺血后心脏中,NCX和CSQ在mRNA水平上的表达显著高于对照组。相比之下,与未缺血对照组相比,新生兔心脏中SERCA的表达保持不变,而成年兔心脏中SERCA的表达下降。
这些发现表明,钙处理蛋白基因表达的变化可能与新生兔心脏和成年兔心脏在缺血后发生心肌功能障碍的易感性不同有关。