## Abstract Low pH appears to enhance the effectiveness of therapeutic hyperthermia. ^13^C and ^31^P NMR spectroscopy have been employed to examine the possibility that elevating glucose in a solid tumor while simultaneously reducing tumor blood flow would induce a more profound acidosis than eithe
In Vivo13C NMR spectroscopy of glucose metabolism of RIF-1 tumors
✍ Scribed by Ioannis Constantinidis; John C. Chatham; Janna P. Wehrle; Jerry D. Glickson
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 611 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
An efficient method for measuring in vivo ^13^C NMR spectra of tumors has been developed and employed to monitor glucose metabolism in radiation‐induced fibrosarcomas (RIF‐1) subcutaneously implanted in C3H/HeN mice. [1‐^13^C]Glucose was injected directly into the tumors at a dose of 1 g/kg body wt. Spectra were obtained with a Bruker AM 360‐WB spectrometer (8.4 T/8.9 cm bore) employing a homebuilt probe equipped with a four‐turn solenoidal coil (1.5 cm outer diameter) for detection of ^13^C signals and a Helmholtz coil (two 3‐cm turns separated by a 3‐cm gap, oriented orthogonally to the ^13^C coil) for ^1^H decoupling. In addition to the natural abundance ^13^C resonances of the tumors, signals were detected from the α‐and β‐anomers of labeled glucose. Within 15 min following injection of labeled glucose [3‐^13^C]lactate and [3‐^13^C]alanine were detected. Lactate labeling approached steady state levels within about 50 min after glucose injection; in contrast, alanine labeling increased continuously over the duration of the experiment (70 min). Sixty minutes after glucose injection, the ratio of the intensity of [3‐ ^13^C]lactate to the principal lipid methylene resonance (30 ppm from external tetramethylsilane), which served as an internal intensity reference, was correlated with tumor size, whereas the corresponding ratio of the [3‐ ^13^C] alanine resonance was not. Labeling of glutamate was below the level of detection in the in vivo spectra; however, labeling of C~4~‐glutamate at a level approximately 50‐fold lower than the level of [3‐ ^13^C]lactate was detected in perchloric acid extracts. Incorporation of ^13^C label into C~2~‐and C~3~‐glutamate and C~2~‐lactate was also observed. © 1991 Academic Press, Inc.
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