Department of Radiology, Hadassah Medical Center, Hebrew University of Jerusalem, The Faculty of Medicine, Jerusalem, Israel.
NMR Biomed. 2021 Feb;34(2):e4444. doi: 10.1002/nbm.4444. Epub 2020 Dec 1.
Cardiovascular diseases account for more than 30% of all deaths worldwide and many could be ameliorated with early diagnosis. Current cardiac imaging modalities can assess blood flow, heart anatomy and mechanical function. However, for early diagnosis and improved treatment, further functional biomarkers are needed. One such functional biomarker could be the myocardium pH. Although tissue pH is already determinable via MR techniques, and has been since the early 1990s, it remains elusive to use practically. The objective of this study was to explore the possibility to evaluate cardiac pH noninvasively, using in-cell enzymatic rates of hyperpolarized [1- C]pyruvate metabolism (ie, moles of product produced per unit time) determined directly in real time using magnetic resonance spectroscopy in a perfused mouse heart model. As a gold standard for tissue pH we used P spectroscopy and the chemical shift of the inorganic phosphate (Pi) signal. The nonhomogenous pH distribution of the perfused heart was analyzed using a multi-parametric analysis of this signal, thus taking into account the heterogeneous nature of this characteristic. As opposed to the signal ratio of hyperpolarized [ C]bicarbonate to [ CO ], which has shown correlation to pH in other studies, we investigated here the ratio of two intracellular enzymatic rates: lactate dehydrogenase (LDH) and pyruvate dehydrogenase (PDH), by way of determining the production rates of [1- C]lactate and [ C]bicarbonate, respectively. The enzyme activities determined here are intracellular, while the pH determined using the Pi signal may contain an extracellular component, which could not be ruled out. Nevertheless, we report a strong correlation between the tissue pH and the LDH/PDH activities ratio. This work may pave the way for using the LDH/PDH activities ratio as an indicator of cardiac intracellular pH in vivo, in an MRI examination.
心血管疾病占全球所有死亡人数的 30%以上,许多疾病可以通过早期诊断得到改善。目前的心脏成像方式可以评估血流、心脏解剖结构和机械功能。然而,为了进行早期诊断和改善治疗,还需要进一步的功能生物标志物。一种这样的功能生物标志物可能是心肌 pH 值。尽管组织 pH 值已经可以通过磁共振技术来确定,并且自 20 世纪 90 年代初以来就已经可以确定,但实际上仍然难以使用。本研究的目的是探索使用超极化 [1- C]丙酮酸代谢的细胞内酶反应率(即单位时间内产生的产物摩尔数)来非侵入性地评估心脏 pH 值的可能性,该反应率直接使用磁共振光谱技术在灌注的小鼠心脏模型中实时确定。作为组织 pH 值的金标准,我们使用 P 光谱和无机磷酸盐 (Pi) 信号的化学位移。使用这种信号的多参数分析来分析灌注心脏的不均匀 pH 值分布,从而考虑到这种特征的不均匀性质。与其他研究中显示与 pH 值相关的超极化 [ C]碳酸氢盐与 [ CO ]的信号比相反,我们在这里研究了两种细胞内酶反应率的比值:乳酸脱氢酶 (LDH) 和丙酮酸脱氢酶 (PDH),通过分别确定 [1- C]乳酸和 [ C]碳酸氢盐的产生速率。这里确定的酶活性是细胞内的,而使用 Pi 信号确定的 pH 值可能包含细胞外成分,这无法排除。尽管如此,我们报告了组织 pH 值与 LDH/PDH 活性比之间的强相关性。这项工作可能为在 MRI 检查中使用 LDH/PDH 活性比作为心脏细胞内 pH 值的体内指标铺平道路。