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Pacing-Induced Regional Differences in Adenosine Receptors mRNA Expression in a Swine Model of Dilated Cardiomyopathy

机译:在腺苷受体mRNa表达起搏诱导的地区差异在扩张型心肌病的猪模型

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摘要

The adenosinergic system is essential in the mediation of intrinsic protection and myocardial resistance to insu it may be considered a cardioprotective molecule and adenosine receptors (ARs) represent potential therapeutic targets in the setting of heart failure (HF). The aim of the study was to test whether differences exist between mRNA expression of ARs in the anterior left ventricle (LV) wall (pacing site: PS) compared to the infero septal wall (opposite region: OS) in an experimental model of dilated cardiomyopathy. Cardiac tissue was collected from LV PS and OS of adult male minipigs with pacing-induced HF (n = 10) and from a control group (C, n = 4). ARs and TNF–α mRNA expression was measured by Real Time-PCR and the results were normalized with the three most stably expressed genes (GAPDH, HPRT1, TBP). Immunohistochemistry analysis was also performed. After 3 weeks of pacing higher levels of expression for each analyzed AR were observed in PS except for A1R (A1R: C = 0.6±0.2, PS = 0.1±0.04, OS = 0.04±0.01, p<0.0001 C vs. PS and OS respectively; A2AR: C = 1.04±0.59, PS = 2.62±0.79, OS = 2.99±0.79; A2BR: C = 1.2±0.1, PS = 5.59±2.3, OS = 1.59±0.46; A3R: C = 0.76±0.18, PS = 8.40±3.38, OS = 4.40±0.83). Significant contractile impairment and myocardial hypoperfusion were observed at PS after three weeks of pacing as compared to OS. TNF-α mRNA expression resulted similar in PS (6.3±2.4) and in OS (5.9±2.7) although higher than in control group (3.4±1.5). ARs expression was mainly detected in cardiomyocytes. This study provided new information on ARs local changes in the setting of LV dysfunction and on the role of these receptors in relation to pacing-induced abnormalities of myocardial perfusion and contraction. These results suggest a possible therapeutic role of adenosine in patients with HF and dyssynchronous LV contraction.
机译:腺苷能系统在调节内在保护和心肌对侮辱的抵抗力中至关重要。它可能被认为是一种心脏保护分子,腺苷受体(ARs)代表了心力衰竭(HF)的潜在治疗靶点。这项研究的目的是检验在扩张型心肌病的实验模型中,左前房室壁(起搏部位:PS)与下隔间隔壁(相对部位:OS)之间AR的mRNA表达是否存在差异。从具有起搏诱导的HF的成年雄性小型猪的LV PS和OS(n = 10)和对照组(C,n = 4)收集心脏组织。通过实时荧光定量PCR检测ARs和TNF-αmRNA的表达,并使用三个最稳定表达的基因(GAPDH,HPRT1,TBP)对结果进行标准化。还进行了免疫组织化学分析。起搏3周后,除A1R以外,PS中每个分析的AR均有更高的表达水平(A1R:C = 0.6±0.2,PS = 0.1±0.04,OS = 0.04±0.01,p <0.0001 C vs.PS和OS分别为; A2AR:C = 1.04±0.59,PS = 2.62±0.79,OS = 2.99±0.79; A2BR:C = 1.2±0.1,PS = 5.59±2.3,OS = 1.59±0.46; A3R:C = 0.76±0.18, PS = 8.40±3.38,OS = 4.40±0.83)。与OS相比,起搏三周后在PS处观察到显着的收缩损伤和心肌灌注不足。 PS(6.3±2.4)和OS(5.9±2.7)中的TNF-αmRNA表达相似,但高于对照组(3.4±1.5)。 ARs表达主要在心肌细胞中检测到。这项研究提供了有关ARs在LV功能障碍中的局部变化以及这些受体在起搏诱导的心肌灌注和收缩异常中的作用的新信息。这些结果表明腺苷在心力衰竭和左室收缩不同步的患者中可能具有治疗作用。

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