Assessing inflammatory liver injury in an acute CCl4 model using dynamic 3D metabolic imaging of hyperpolarized [1-13C]pyruvate

被引:51
作者
Josan, Sonal [1 ,2 ]
Billingsley, Kelvin [2 ,3 ]
Orduna, Juan [1 ]
Park, Jae Mo [2 ]
Luong, Richard [4 ]
Yu, Liqing [5 ]
Hurd, Ralph [6 ]
Pfefferbaum, Adolf [1 ,7 ]
Spielman, Daniel [2 ]
Mayer, Dirk [1 ,2 ,8 ]
机构
[1] SRI Int, Neurosci Program, Menlo Pk, CA 94025 USA
[2] Stanford Univ, Dept Radiol, Stanford, CA 94305 USA
[3] San Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USA
[4] Stanford Univ, Dept Comparat Med, Stanford, CA 94305 USA
[5] Univ Maryland, Dept Anim & Avian Sci, College Pk, MD 20742 USA
[6] GE Healthcare Appl Sci Lab, Menlo Pk, CA USA
[7] Stanford Univ, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[8] Univ Maryland, Dept Diagnost Radiol & Nucl Med, Baltimore, MD 21201 USA
关键词
hyperpolarized C-13; CCl4; liver; inflammation; CARBON-TETRACHLORIDE; UNITED-STATES; RAT-LIVER; DISEASE; SPECTROSCOPY; BIOPSY; C-13-PYRUVATE; PREVALENCE; PYRUVATE; DAMAGE;
D O I
10.1002/nbm.3431
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To facilitate diagnosis and staging of liver disease, sensitive and non-invasive methods for the measurement of liver metabolism are needed. This study used hyperpolarized C-13-pyruvate to assess metabolic parameters in a CCl4 model of liver damage in rats. Dynamic 3D C-13 chemical shift imaging data from a volume covering kidney and liver were acquired from 8 control and 10 CCl4-treated rats. At 12 time points at 5 s temporal resolution, we quantified the signal intensities and established time courses for pyruvate, alanine, and lactate. These measurements were compared with standard liver histology and an alanine transaminase (ALT) enzyme assay using liver tissue from the same animals. All CCl4-treated but none of the control animals showed histological liver damage and elevated ALT enzyme levels. In agreement with these results, metabolic imaging revealed an increased alanine/pyruvate ratio in liver of CCl4-treated rats, which is indicative of elevated ALT activity. Similarly, lactate/pyruvate ratios were higher in CCl4-treated compared with control animals, demonstrating the presence of inflammation. No significant differences in metabolite ratios were observed in kidney or vasculature. Thus this work shows that metabolic imaging using C-13-pyruvate can be a successful tool to non-invasively assess liver damage in vivo. Copyright (C) 2015 John Wiley & Sons, Ltd.
引用
收藏
页码:1671 / 1677
页数:7
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