Non-invasive assessment of hepatic mitochondrial metabolism by positional isotopomer NMR tracer analysis (PINTA)

被引:47
作者
Perry, Rachel J. [1 ]
Peng, Liang [1 ]
Cline, Gary W. [1 ]
Butrico, Gina M. [1 ]
Wang, Yongliang [1 ]
Zhang, Xian-Man [1 ]
Rothman, Douglas L. [2 ,3 ,4 ]
Petersen, Kitt Falk [1 ]
Shulman, Gerald I. [1 ,5 ,6 ,7 ]
机构
[1] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Radiol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Biomed Imaging, New Haven, CT 06520 USA
[4] Yale Univ, Dept Biomed Engn, Sch Med, New Haven, CT 06520 USA
[5] Yale Univ, Dept Cellular, Sch Med, New Haven, CT 06520 USA
[6] Yale Univ, Dept Mol Physiol, Sch Med, New Haven, CT 06520 USA
[7] Yale Univ, Dept Howard Hughes Med Inst, Sch Med, New Haven, CT 06520 USA
关键词
FATTY LIVER-DISEASE; INSULIN-RESISTANCE; GLUCOSE-PRODUCTION; ACID CYCLE; C-13; NMR; IN-VIVO; FASTED STATE; TCA CYCLE; GLUCONEOGENESIS; PYRUVATE;
D O I
10.1038/s41467-017-01143-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hepatic mitochondria play a central role in the regulation of intermediary metabolism and maintenance of normoglycemia, and there is great interest in assessing rates of hepatic mitochondrial citrate synthase flux (VCS) and pyruvate carboxylase flux (VPC) in vivo. Here, we show that a positional isotopomer NMR tracer analysis (PINTA) method can be used to non-invasively assess rates of VCS and VPC fluxes using a combined NMR/gas chromatography-mass spectrometry analysis of plasma following infusion of [3-C-13] lactate and glucose tracer. PINTA measures VCS and VPC fluxes over a wide range of physiological conditions with minimal pyruvate cycling and detects increased hepatic VCS following treatment with a liver-targeted mitochondrial uncoupler. Finally, validation studies in humans demonstrate that the VPC/VCS ratio measured by PINTA is similar to that determined by in vivo NMR spectroscopy. This method will provide investigators with a relatively simple tool to non-invasively examine the role of altered hepatic mitochondrial metabolism.
引用
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页数:9
相关论文
共 44 条
[1]   A controlled-release mitochondrial protonophore reverses hypertriglyceridemia, nonalcoholic steatohepatitis, and diabetes in lipodystrophic mice [J].
Abulizi, Abudukadier ;
Perry, Rachel J. ;
Camporez, Joao Paulo G. ;
Jurczak, Michael J. ;
Petersen, Kitt Falk ;
Aspichueta, Patricia ;
Shulman, Gerald I. .
FASEB JOURNAL, 2017, 31 (07) :2916-2924
[2]   Measuring Deuterium Enrichment of Glucose Hydrogen Atoms by Gas Chromatography/Mass Spectrometry [J].
Antoniewicz, Maciek R. ;
Kelleher, Joanne K. ;
Stephanopoulos, Gregory .
ANALYTICAL CHEMISTRY, 2011, 83 (08) :3211-3216
[3]  
Befroy DE, 2015, NAT MED, V21, DOI 10.1038/nm.3790
[4]   Direct assessment of hepatic mitochondrial oxidative and anaplerotic fluxes in humans using dynamic 13C magnetic resonance spectroscopy [J].
Befroy, Douglas E. ;
Perry, Rachel J. ;
Jain, Nimit ;
Dufour, Sylvie ;
Cline, Gary W. ;
Trimmer, Jeff K. ;
Brosnan, Julia ;
Rothman, Douglas L. ;
Petersen, Kitt Falk ;
Shulman, Gerald I. .
NATURE MEDICINE, 2014, 20 (01) :98-+
[5]   Noninvasive evaluation of liver metabolism by 2H and 13C NMR isotopomer analysis of human urine [J].
Burgess, SC ;
Weis, B ;
Jones, JG ;
Smith, E ;
Merritt, ME ;
Margolis, D ;
Sherry, AD ;
Malloy, CR .
ANALYTICAL BIOCHEMISTRY, 2003, 312 (02) :228-234
[6]   Influence of obesity and type 2 diabetes on gluconeogenesis and glucose output in humans - A quantitative study [J].
Gastaldelli, A ;
Baldi, S ;
Pettiti, M ;
Toschi, E ;
Camastra, S ;
Natali, A ;
Landau, BR ;
Ferrannini, E .
DIABETES, 2000, 49 (08) :1367-1373
[7]   Phosphoenolpyruvate carboxykinase and the critical role of cataplerosis in the control of hepatic metabolism [J].
Hakimi P. ;
Johnson M.T. ;
Yang J. ;
Lepage D.F. ;
Conlon R.A. ;
Kalhan S.C. ;
Reshef L. ;
Tilghman S.M. ;
Hanson R.W. .
Nutrition & Metabolism, 2 (1)
[8]   Acetyl-CoA carboxylase inhibition by ND-630 reduces hepatic steatosis, improves insulin sensitivity, and modulates dyslipidemia in rats [J].
Harriman, Geraldine ;
Greenwood, Jeremy ;
Bhat, Sathesh ;
Huang, Xinyi ;
Wang, Ruiying ;
Paul, Debamita ;
Tong, Liang ;
Saha, Asish K. ;
Westlin, William F. ;
Kapeller, Rosana ;
Harwood, H. James, Jr. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (13) :E1796-E1805
[9]   Mass spectrometry-based microassay of 2H and 13C plasma glucose labeling to quantify liver metabolic fluxes in vivo [J].
Hasenour, Clinton M. ;
Wall, Martha L. ;
Ridley, D. Emerson ;
Hughey, Curtis C. ;
James, Freyja D. ;
Wasserman, David H. ;
Young, Jamey D. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2015, 309 (02) :E191-E203
[10]  
HELLERSTEIN MK, 1992, AM J PHYSIOL, V263, pE988