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在心脏缺血再灌注期间,醛糖还原酶通过β-连环蛋白途径调节间充质标志物的急性激活。

Aldose reductase modulates acute activation of mesenchymal markers via the β-catenin pathway during cardiac ischemia-reperfusion.

作者信息

Thiagarajan Devi, O' Shea Karen, Sreejit Gopalkrishna, Ananthakrishnan Radha, Quadri Nosirudeen, Li Qing, Schmidt Ann Marie, Gabbay Kenneth, Ramasamy Ravichandran

机构信息

Diabetes Research Program, Department of Medicine, New York University Langone Medical Center, New York, New York, United States of America.

Department of Pediatrics, Children's Nutrition Research Center, Baylor College of Medicine, Houston, Texas, United States of America.

出版信息

PLoS One. 2017 Nov 30;12(11):e0188981. doi: 10.1371/journal.pone.0188981. eCollection 2017.

Abstract

Aldose reductase (AR: human, AKR1B1; mouse, AKR1B3), the first enzyme in the polyol pathway, plays a key role in mediating myocardial ischemia/reperfusion (I/R) injury. In earlier studies, using transgenic mice broadly expressing human AKR1B1 to human-relevant levels, mice devoid of Akr1b3, and pharmacological inhibitors of AR, we demonstrated that AR is an important component of myocardial I/R injury and that inhibition of this enzyme protects the heart from I/R injury. In this study, our objective was to investigate if AR modulates the β-catenin pathway and consequent activation of mesenchymal markers during I/R in the heart. To test this premise, we used two different experimental models: in vivo, Akr1b3 null mice and wild type C57BL/6 mice (WT) were exposed to acute occlusion of the left anterior descending coronary artery (LAD) followed by recovery for 48 hours or 28 days, and ex-vivo, WT and Akr1b3 null murine hearts were perfused using the Langendorff technique (LT) and subjected to 30 min of global (zero-flow) ischemia followed by 60 min of reperfusion. Our in vivo results reveal reduced infarct size and improved functional recovery at 48 hours in mice devoid of Akr1b3 compared to WT mice. We demonstrate that the cardioprotection observed in Akr1b3 null mice was linked to acute activation of the β-catenin pathway and consequent activation of mesenchymal markers and genes linked to fibrotic remodeling. The increased activity of the β-catenin pathway at 48 hours of recovery post-LAD was not observed at 28 days post-infarction, thus indicating that the observed increase in β-catenin activity was transient in the mice hearts devoid of Akr1b3. In ex vivo studies, inhibition of β-catenin blocked the cardioprotection observed in Akr1b3 null mice hearts. Taken together, these data indicate that AR suppresses acute activation of β-catenin and, thereby, blocks consequent induction of mesenchymal markers during early reperfusion after myocardial ischemia. Inhibition of AR might provide a therapeutic opportunity to optimize cardiac remodeling after I/R injury.

摘要

醛糖还原酶(AR:人类为AKR1B1;小鼠为AKR1B3)是多元醇途径中的首个酶,在介导心肌缺血/再灌注(I/R)损伤中起关键作用。在早期研究中,我们使用广泛表达人类AKR1B1至与人类相关水平的转基因小鼠、缺乏Akr1b3的小鼠以及AR的药理学抑制剂,证明AR是心肌I/R损伤的重要组成部分,并且抑制该酶可保护心脏免受I/R损伤。在本研究中,我们的目的是调查AR是否在心脏I/R期间调节β-连环蛋白途径以及随后间充质标志物的激活。为了验证这一前提,我们使用了两种不同的实验模型:在体内,将Akr1b3基因敲除小鼠和野生型C57BL/6小鼠(WT)暴露于左前降支冠状动脉(LAD)急性闭塞后恢复48小时或28天;在体外,使用Langendorff技术(LT)灌注WT和Akr1b3基因敲除小鼠的心脏,并使其经历30分钟的全心(零流量)缺血,随后再灌注60分钟。我们的体内结果显示,与WT小鼠相比,缺乏Akr1b3的小鼠在48小时时梗死面积减小,功能恢复改善。我们证明在Akr1b3基因敲除小鼠中观察到的心脏保护作用与β-连环蛋白途径的急性激活以及随后间充质标志物和与纤维化重塑相关基因的激活有关。在LAD后恢复48小时时β-连环蛋白途径的活性增加在梗死后28天时未观察到,因此表明在缺乏Akr1b3的小鼠心脏中观察到的β-连环蛋白活性增加是短暂的。在体外研究中,抑制β-连环蛋白可阻断在Akr1b3基因敲除小鼠心脏中观察到的心脏保护作用。综上所述,这些数据表明AR抑制β-连环蛋白的急性激活,从而在心肌缺血后的早期再灌注期间阻断随后间充质标志物的诱导。抑制AR可能为优化I/R损伤后的心脏重塑提供治疗机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6c8/5708684/d68ad6f9c2cd/pone.0188981.g001.jpg

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