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用 1-13C 标记的丙酮酸评估与肾缺血再灌注损伤进展相关的代谢重编程。

Metabolic reprogramming associated with progression of renal ischemia reperfusion injury assessed with hyperpolarized [1-C]pyruvate.

机构信息

MR Research Centre, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

出版信息

Sci Rep. 2020 Jun 2;10(1):8915. doi: 10.1038/s41598-020-65816-1.

Abstract

Acute kidney injury is a major clinical challenge affecting as many as 1 percent of all hospitalized patients. Currently it is not possible to accurately stratify and predict the outcome of the individual patient. Increasing evidence supports metabolic reprogramming as a potential target for new biomarkers. Hyperpolarized [1-C]pyruvate imaging is a promising new tool for evaluating the metabolic status directly in the kidneys. We here investigate the prognostic potential of hyperpolarized [1-C]pyruvate in the setting of acute kidney injury in a rodent model of ischemia reperfusion. A significant correlation was found between the intra-renal metabolic profile 24 hours after reperfusion and 7 days after injury induction, as well as a correlation with the conventional plasma creatinine biomarker of renal function and markers of renal injury. This leads to a possible outcome prediction of renal function and injury development from a metabolic profile measured in vivo. The results support human translation of this new technology to renal patients as all experiements have been performed using clinical MRI equipment.

摘要

急性肾损伤是一个主要的临床挑战,影响多达 1%的住院患者。目前,还不可能对个体患者的病情进行准确分层和预测。越来越多的证据支持代谢重编程作为新生物标志物的潜在靶点。极化 [1-C]丙酮酸成像是一种有前途的新工具,可直接在肾脏中评估代谢状态。我们在这里研究了在缺血再灌注的啮齿动物模型中,极化 [1-C]丙酮酸在急性肾损伤中的预后潜力。在再灌注后 24 小时内,发现了肾脏内代谢谱与损伤诱导后 7 天之间的显著相关性,以及与常规血浆肌酐肾功能生物标志物和肾损伤标志物的相关性。这导致了从体内测量的代谢谱来预测肾功能和损伤发展的可能结果。这些结果支持将这项新技术应用于肾患者,因为所有实验都是使用临床 MRI 设备进行的。

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