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首页> 外文期刊>Journal of cardiovascular translational research. >Myocardial Injury Promotes Matrix Metalloproteinase-9 Activity in the Renal Cortex in Preclinical Models of Acute Myocardial Infarction
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Myocardial Injury Promotes Matrix Metalloproteinase-9 Activity in the Renal Cortex in Preclinical Models of Acute Myocardial Infarction

机译:在急性心肌梗死的临床前模型中,心肌损伤促进肾皮层中基质金属蛋白酶-9的活性

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New mechanistic insight into how the kidney responds to cardiac injury during acute myocardial infarction (AMI) is required. We hypothesized that AMI promotes inflammation and matrix metalloproteinase-9 (MMP9) activity in the kidney and studied the effect of initiating an Impella CP or veno-arterial extracorporeal membrane oxygenation (VA-ECMO) before coronary reperfusion during AMI. Adult male swine were subjected to coronary occlusion and either reperfusion (ischemia-reperfusion; IR) or support with either Impella or VA-ECMO before reperfusion. IR and ECMO increased while Impella reduced levels of MMP-9 in the myocardial infarct zone, circulation, and renal cortex. Compared to IR, Impella reduced myocardial infarct size and urinary KIM-1 levels, but VA-ECMO did not. IR and VA-ECMO increased pro-fibrogenic signaling via transforming growth factor-beta and endoglin in the renal cortex, but Impella did not. These findings identify that AMI increases inflammatory activity in the kidney, which may be attenuated by Impella support.
机译:需要对急性心肌梗死 (AMI) 期间肾脏如何对心脏损伤做出反应的新机制见解。我们假设 AMI 促进肾脏中的炎症和基质金属蛋白酶-9 (MMP9) 活性,并研究了在 AMI 期间冠状动脉再灌注之前启动 Impella CP 或静脉动脉体外膜肺氧合 (VA-ECMO) 的效果。成年雄性猪进行冠状动脉闭塞和再灌注(缺血再灌注;IR) 或在再灌注前使用 Impella 或 VA-ECMO 支持。IR 和 ECMO 增加,而 Impella 降低心肌梗死区、循环和肾皮质中 MMP-9 的水平。与 IR 相比,Impella 减少了心肌梗死面积和尿液 KIM-1 水平,但 VA-ECMO 没有。 IR 和 VA-ECMO 通过转化肾皮质中的生长因子-β 和内皮蛋白来增加促纤维化信号传导,但 Impella 没有。这些发现表明,AMI增加了肾脏的炎症活动,而Impella支持可能会减弱炎症活动。

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