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腹主动脉阻断再灌注引起的心功能障碍可以被 MitoTEMPO 预防。

Abdominal Ischemia-Reperfusion Induced Cardiac Dysfunction Can Be Prevented by MitoTEMPO.

机构信息

Taskent Vocational School, Department of Occupational Health and Safety, Selcuk University, Konya, Turkey.

Meram Faculty of Medicine, Department of Biophysics, Necmettin Erbakan University, Konya, Turkey.

出版信息

J Invest Surg. 2022 Mar;35(3):577-583. doi: 10.1080/08941939.2021.1902593. Epub 2021 Mar 25.

Abstract

BACKGROUND

Cardiac dysfunction is secondary to acute mesenteric ischemia (AMI) and abdominal aortic aneurysms (AAA). The underlying cause of distant organ damage in the heart is the formation of oxidative stress caused by ischemia-reperfusion. In this study, we investigated the possible protective effects of a novel mitochondria-targeted antioxidant MitoTEMPO on contractile dysfunction and structural defects of the rat papillary muscle caused by abdominal ischemia-reperfusion (AIR).

METHODS AND RESULTS

In the experiments, adult Wistar-Albino rats were used and animals were divided randomly into 3 groups; sham-operated group (SHAM), an IR group that had aortic cross-clamping for 1 h followed by 2 h reperfusion, and a third group that received protective 0.7 mg/kg/day MitoTEMPO injection for 28-day before IR. As a result, it was observed that MitoTEMPO injection had a protective effect on the mechanical activities and structural properties of the papillary muscle impaired by AIR. Our study also showed that AIR disrupted the contractile function of the papillary muscle for each stimulation frequency and post-potentiation responses tested. This is common for each measured and calculated mechanical parameter and MitoTEMPO injection showed its protective effects.

CONCLUSION

Consequently, calcium homeostasis seems to be impaired by AIR, and MitoTEMPO may exert its protective effect through energy metabolism by directly targeting the mitochondria.

摘要

背景

心脏功能障碍是急性肠系膜缺血(AMI)和腹主动脉瘤(AAA)的继发症。导致心脏远处器官损伤的根本原因是缺血再灌注引起的氧化应激形成。在这项研究中,我们研究了新型线粒体靶向抗氧化剂 MitoTEMPO 对腹部缺血再灌注(AIR)引起的大鼠乳头肌收缩功能障碍和结构缺陷的可能保护作用。

方法和结果

在实验中,使用成年 Wistar-Albino 大鼠,将动物随机分为 3 组;假手术组(SHAM)、主动脉夹闭 1 小时然后再灌注 2 小时的 IR 组,以及在 IR 前 28 天每天接受 0.7mg/kg MitoTEMPO 注射的第三组。结果表明,MitoTEMPO 注射对 AIR 损伤的乳头肌机械活动和结构特性具有保护作用。我们的研究还表明,AIR 破坏了乳头肌对每种刺激频率和后增强反应的收缩功能。这对于每个测量和计算的机械参数都是常见的,并且 MitoTEMPO 注射显示出其保护作用。

结论

因此,AIR 似乎破坏了钙稳态,MitoTEMPO 可能通过直接靶向线粒体来通过能量代谢发挥其保护作用。

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