In Vivo Magnetic Resonance Studies of Glycine and Glutathione Metabolism in a Rat Mammary Tumor

• Published in: NMR in biomedicine 2011-07, Vol.25 (2), p.271-278
• Main Authors: Thelwall, Peter E., Simpson, Nicholas E., Rabbani, Zahid N., Clark, M. Daniel, Pourdeyhimi, Roxana, Macdonald, Jeffrey M., Blackband, Stephen J., Gamcsik, Michael P.
• Format: Article
• Language: English
• ISSN: 0952-3480; 1099-1492
• DOI: 10.1002/nbm.1745

The metabolism of glycine into glutathione was monitored noninvasively in vivo in intact R3230Ac rat tumors by magnetic resonance imaging and spectroscopy. Metabolism was tracked by following the isotope label from intravenously infused [2- 13 C]-glycine into the glycinyl residue of glutathione. Signals from [2- 13 C]-glycine and γ-glutamylcysteinyl-[2- 13 C]-glycine ( 13 C-glutathione) were detected by nonlocalized 13 C spectroscopy as these resonances are distinct from background signals. In addition, using spectroscopic imaging methods, heterogeneity in the in vivo tumor distribution of glutathione was observed. In vivo spectroscopy also detected isotope incorporation from [2- 13 C]-glycine into both the 2- and 3-carbons of serine. Analyses of tumor tissue extracts show single and multiple label incorporation from [2- 13 C]-glycine into serine from metabolism through the serine hydroxymethyltransferase and glycine cleavage system pathways. Mass spectrometric analysis of extracts also shows that isotope-labeled serine is further metabolized via the transsulfuration pathway as the 13 C-isotope labels appear in both the glycinyl- and the cysteinyl-residue of glutathione. Our studies demonstrate the use of magnetic resonance imaging and spectroscopy for monitoring tumor metabolic processes central to oxidative stress defense.