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Sigma-1 受体激动剂 PRE-084 改善大鼠心肌缺血再灌注损伤。

Sigma-1 Receptor Stimulation with PRE-084 Ameliorates Myocardial Ischemia-Reperfusion Injury in Rats.

机构信息

Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430000; Department of Cardiology, First Hospital of Jingmen, Jingmen, Hubei 448000, China.

Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430000, China.

出版信息

Chin Med J (Engl). 2018 Mar 5;131(5):539-543. doi: 10.4103/0366-6999.226076.

Abstract

BACKGROUND

The sigma receptors are a relatively novel receptor group with respect to knowledge of their effect on health. Although the sigma-1 receptor agonist PRE-084 exhibits a cardioprotective effect in some studies, the benefits in cases of myocardial ischemia/reperfusion (I/R) are not clear. The aim of this study was to explore the mechanism of action and assess the effect of PRE-084 on myocardial I/R injury in rats.

METHODS

In this study, rats were assigned randomly to three groups with computer (n = 14 for each group): a sham group, an I/R group, and a PRE-084 group. In the PRE-084 group, rats were administered PRE-084 1 h before operation. In the myocardial I/R model, the left anterior descending branch of rats was ligated and opened half an hour later. Cardiac function was assessed, and the apoptosis index was evaluated. The mechanisms of the cardioprotective effects of PRE-084 were explored.

RESULTS

PRE-084 pretreatment preserved cardiac function and reduced myocardial apoptosis (F = 86.0, P < 0.01) with Western blotting analysis, showing significantly reduced expression of Bax (F = 75.7, P < 0.01) and cleaved-caspase 3 (F = 44.7, P < 0.01), along with increased expression of the Bcl-2 protein (P < 0.01) and phosphorylated protein kinase B (p-Akt) (P < 0.01) and phosphorylated-endothelial nitric oxide synthase (p-eNOS; P < 0.01).

CONCLUSION

PRE-084 preserved cardiac function and reduced myocardial apoptosis through the activation of Akt and eNOS.

摘要

背景

相对于人们对其健康影响的了解,sigma 受体是一个相对较新的受体群体。虽然 sigma-1 受体激动剂 PRE-084 在一些研究中表现出心脏保护作用,但在心肌缺血/再灌注(I/R)的情况下其益处尚不清楚。本研究旨在探讨 PRE-084 的作用机制,并评估其对大鼠心肌 I/R 损伤的影响。

方法

本研究中,大鼠随机分为三组(每组 14 只):假手术组、I/R 组和 PRE-084 组。在 PRE-084 组中,大鼠在手术前 1 小时给予 PRE-084。在心肌 I/R 模型中,结扎大鼠的左前降支,半小时后再灌注。评估心脏功能并评估细胞凋亡指数。探讨 PRE-084 心脏保护作用的机制。

结果

PRE-084 预处理可保存心脏功能并减少心肌细胞凋亡(F = 86.0,P < 0.01),Western blot 分析显示 Bax 表达明显减少(F = 75.7,P < 0.01)和 cleaved-caspase 3(F = 44.7,P < 0.01),同时 Bcl-2 蛋白(P < 0.01)和磷酸化蛋白激酶 B(p-Akt)(P < 0.01)和磷酸化内皮型一氧化氮合酶(p-eNOS;P < 0.01)表达增加。

结论

PRE-084 通过激活 Akt 和 eNOS 来保存心脏功能并减少心肌细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6962/5850669/392cb2b0d3f3/CMJ-131-539-g001.jpg

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