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不同的心脏停搏液如何影响未成熟大鼠缺血/再灌注心脏模型中的基因表达和细胞因子反应?

How different cardioplegic solutions influence genes expression and cytokine response in an immature rat heart model of ischemia/reperfusion?

作者信息

Mamedov Arslan, Gečys Dovydas, Jakuška Povilas, Treinys Rimantas, Narauskaitė Deimantė, Aitaliyev Serik, Rumbinaitė Eglė, Karčiauskas Dainius, Benetis Rimantas, Stankevičius Edgaras

机构信息

Department of Cardiac, Thoracic and Vascular Surgery, Faculty of Medicine, Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.

Laboratory of Molecular Cardiology, Institute of Cardiology, Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.

出版信息

PLoS One. 2025 Jul 29;20(7):e0329010. doi: 10.1371/journal.pone.0329010. eCollection 2025.

Abstract

INTRODUCTION

The use of cardioplegia not only achieves cardiac arrest but also minimizes ischemic/reperfusion (I/R) injury, potentially improving short- or long-term outcomes. The aim of this study was to evaluate the impact of different cardioplegic solutions - del Nido, Custodiol HTK and St. Thomas on genes expression and cytokines response in an immature rat heart model of I/R using the Langendorff preparation. Expression of genes which are involved in cell cycle, proliferation, apoptosis resistance and response to hypoxia were determined in cardiac tissue, as well as levels pro/anti-inflammatory cytokines were measured.

METHODS

A total of 39 male Wistar albino rats were utilized in this study. Experimental animals were divided into 3 groups, four animals in each following groups: St. Thomas (ST), Custodiol HTK (HTK) and del Nido (DN) group. Moreover, each of these groups was divided into 3 groups according to ischemia's time: 1h ischemia with 20 min reperfusion time, 2h ischemia with 40 min reperfusion time, 4h ischemia with 80 min reperfusion and control groups (K-PRF) with 30 minutes of perfusion was performed in the K-PRF (n = 3). The heart was removed from the chest and immediately frozen at -81°C.

RESULTS

All cardioplegic solutions effectively modulate the expression of HIF1A, FOS, and BNIP2 genes. The results indicated that DN actively induces HIF1A within the first hour. Compared to the ST, and HTK groups, the expression of the HIF1A gene was on average 2 times higher (P < 0.01). Similar results were observed in the 2-hour group. After 4 hours, the effect of cardioplegic solutions continued to maintain the dynamics, but the differences were not statistically significant. The expression of the FOS gene after 2 and 4 hours of incubation with the DN solution remained significantly higher compared to ST (P < 0.05) and HTK (P < 0.05). A comparative analysis with the perfusion group showed that BNIP2 gene expression in the ST and HTK solution groups was significantly lower than in perfused tissue (P < 0.05). Pro-inflammatory cytokines: TNF-alpha, IL-6 and anti-inflammatory cytokines: IL-4 and IL-10 were evaluated. The results showed that there was no statistically significant difference between the groups (P > 0.05).

CONCLUSION

In our experiment, statistically significant differences were not observed in cytokines. Although statistically significant differences were observed only in gene expression, and only in the rat model, the overall results suggest that del Nido cardioplegic solution may provide better cellular protection. It is also worth mentioning that gene expression and cytokines change are not direct markers of cardioprotection. Further research is needed to confirm these results in human tissues and broader clinical settings.

摘要

引言

心脏停搏液的使用不仅能实现心脏停搏,还能将缺血/再灌注(I/R)损伤降至最低,可能改善短期或长期预后。本研究的目的是在使用Langendorff装置的未成熟大鼠心脏I/R模型中,评估不同心脏停搏液——德尔尼多(del Nido)、HTK液(Custodiol HTK)和圣托马斯液(St. Thomas)对基因表达和细胞因子反应的影响。测定了心脏组织中参与细胞周期、增殖、抗凋亡和低氧反应的基因表达,以及促炎/抗炎细胞因子水平。

方法

本研究共使用了39只雄性Wistar白化大鼠。实验动物分为3组,每组4只:圣托马斯液组(ST)、HTK液组(HTK)和德尔尼多液组(DN)。此外,根据缺血时间,每组又分为3组:缺血1小时加再灌注20分钟、缺血2小时加再灌注40分钟、缺血4小时加再灌注80分钟,对照组(K-PRF)进行30分钟灌注(K-PRF组,n = 3)。心脏从胸腔取出后立即在-81°C下冷冻。

结果

所有心脏停搏液均能有效调节低氧诱导因子1α(HIF1A)、原癌基因FOS和Bcl2相互作用蛋白2(BNIP2)基因的表达。结果表明,DN在第1小时内可积极诱导HIF1A表达。与ST组和HTK组相比,HIF1A基因的表达平均高出2倍(P < 0.01)。在2小时组中观察到类似结果。4小时后,心脏停搏液的作用继续维持这种动态变化,但差异无统计学意义。与DN溶液孵育2小时和4小时后,FOS基因的表达与ST组(P < 0.05)和HTK组(P < 0.05)相比仍显著更高。与灌注组的对比分析表明,ST组和HTK溶液组中BNIP2基因的表达显著低于灌注组织(P < 0.05)。评估了促炎细胞因子:肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和抗炎细胞因子:白细胞介素-4(IL-4)和白细胞介素-10。结果表明,各组之间无统计学显著差异(P > 0.05)。

结论

在我们的实验中,细胞因子方面未观察到统计学显著差异。尽管仅在基因表达上观察到统计学显著差异,且仅在大鼠模型中如此,但总体结果表明德尔尼多心脏停搏液可能提供更好的细胞保护。还值得一提的是,基因表达和细胞因子变化并非心脏保护的直接标志物。需要进一步研究在人体组织和更广泛的临床环境中证实这些结果。

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