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聚乙二醇化血红蛋白的一氧化碳形式可保护糖尿病和正常小鼠的心肌免受缺血/再灌注损伤。

Carbon monoxide form of PEGylated hemoglobin protects myocardium against ischemia/reperfusion injury in diabetic and normal mice.

机构信息

Department of Medicine, Diabetes Research Program, New York University Langone Medical Center, New York , NY , USA.

出版信息

Artif Cells Nanomed Biotechnol. 2013 Dec;41(6):428-36. doi: 10.3109/21691401.2012.762370. Epub 2013 Jan 23.

Abstract

We investigated the pre-clinical utility of carbon monoxide form of PEGylated hemoglobin (PEG-Hb also named SANGUINATE(™)) in myocardial infarction (MI) and in particular the response of diabetic tissues to superimposed ischemia/reperfusion injury. SANGUINATE(™) was evaluated in diabetic and normal mice subjected to 30 min of coronary artery ligation followed by either 48 h or 28 days of reperfusion. Our results demonstrate that SANGUINATE(™) was effective in reducing infarct size when administered either prior to left anterior descending coronary artery (LAD) occlusion or during reperfusion. This finding is an important step in exploring the efficacy of a pharmacoinvasive strategy using SANGUINATE(™) in patients with acute coronary syndromes.

摘要

我们研究了一氧化碳形式的聚乙二醇化血红蛋白(PEG-Hb,也称为 SANGUINATE(™))在心肌梗死(MI)中的临床前效用,特别是糖尿病组织对叠加的缺血/再灌注损伤的反应。SANGUINATE(™)在糖尿病和正常小鼠中进行了评估,这些小鼠接受了 30 分钟的冠状动脉结扎,然后进行 48 小时或 28 天的再灌注。我们的结果表明,SANGUINATE(™)在左前降支冠状动脉(LAD)闭塞前或再灌注期间给药均能有效减少梗死面积。这一发现是探索在急性冠状动脉综合征患者中使用 SANGUINATE(™)进行药物侵入性治疗策略疗效的重要一步。

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