Metabolic alterations in acute myocardial ischemia-reperfusion injury and necrosis using in vivo hyperpolarized [1-(13)C] pyruvate MR spectroscopy

利用体内超极化[1-(13)C]丙酮酸磁共振波谱法研究急性心肌缺血再灌注损伤和坏死中的代谢改变

阅读:1

Abstract

This study aimed to investigate real-time early detection of metabolic alteration in a rat model with acute myocardial ischemia-reperfusion (AMI/R) injury and myocardial necrosis, as well as its correlation with intracellular pH level using in vivo hyperpolarized [1-(13)C] pyruvate magnetic resonance spectroscopy (MRS). Hyperpolarized (13)C MRS was performed on the myocardium of 8 sham-operated control rats and 8 rats with AMI/R injury, and 8 sham-operated control rats and 8 rats with AMI-induced necrosis. Also, the correlations of levels of [1-(13)C] metabolites with pH were analyzed by Spearman's correlation test. The AMI/R and necrosis groups showed significantly higher ratios of [1-(13)C] lactate (Lac)/bicarbonate (Bicar) and [1-(13)C] Lac/total carbon (tC), and lower ratios of (13)C Bicar/Lac + alanine (Ala), and (13)C Bicar/tC than those of the sham-operated control group. Moreover, the necrosis group showed significantly higher ratios of [1-(13)C] Lac/Bicar and [1-(13)C] Lac/tC, and lower ratios of (13)C Bicar/Lac + Ala and (13)C Bicar/tC than those of the AMI/R group. These results were consistent with the pattern for in vivo the area under the curve (AUC) ratios. In addition, levels of [1-(13)C] Lac/Bicar and [1-(13)C] Lac/tC were negatively correlated with pH levels, whereas (13)C Bicar/Lac + Ala and (13)C Bicar/tC levels were positively correlated with pH levels. The levels of [1-(13)C] Lac and (13)C Bicar will be helpful for non-invasively evaluating the early stage of AMI/R and necrosis in conjunction with reperfusion injury of the heart. These findings have potential application to real-time evaluation of cardiac malfunction accompanied by changes in intracellular pH level and enzymatic activity.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。