新生兔心肌缺血后Na-Ca2+交换器、SERCA2a和钙调磷酸酶的基因表达。

Biology of the neonate Pub Date : 2006-01-01 Epub Date: 2006-04-25 DOI:10.1159/000092888
Matthias Seehase, Thomas Quentin, Elke Wiludda, Gerhard Hellige, Thomas Paul, Holger Schiffmann
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引用次数: 9

摘要

背景:新生儿心脏在缺氧和/或缺血后比成人心脏更不容易发生心肌功能障碍。细胞内钙稳态的差异可能是导致未成熟心肌钙超载减少的原因,从而观察到对缺血的保护。目的:探讨新生兔和成年兔心脏缺血后钙处理蛋白基因表达的差异。方法:采用离体的顺行灌注兔心脏(2日龄,28日龄,n = 32),进行类似新生儿窒息的心肌缺血和低温模拟。采用实时荧光定量PCR和Western blotting检测钠钙交换器(NCX)、肌内质网Ca2+- atp酶2a (SERCA)和钙sequestrin (CSQ)的基因和蛋白表达。结果:新生儿和成人心脏缺血再灌注后,心肌功能明显下降。在mRNA水平上,新生儿和成人心脏中NCX、SERCA和CSQ的基线表达存在显著差异。在新生儿缺血后心脏中,NCX和CSQ的mRNA表达水平显著高于对照组。相比之下,与非缺血对照组相比,SERCA在新生儿心脏中的表达保持不变,在成人心脏中的表达下降。结论:这些研究结果提示,钙处理蛋白基因表达的变化可能与新生儿心脏缺血后心肌功能障碍易感性的差异有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene expression of the Na-Ca2+ exchanger, SERCA2a and calsequestrin after myocardial ischemia in the neonatal rabbit heart.

Background: 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.

Objective: To assess differences in baseline and post-ischemic gene expression of calcium handling proteins after ischemia in neonatal and adult rabbit hearts.

Methods: 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.

Results: 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.

Conclusion: 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.

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