## Abstract With the use of localized ^13^C MRS in conjunction with [1โ^13^C]โDโglucose infusion, it is possible to study brain glycogen metabolism in vivo. The purpose of this study was to validate in vivo ^13^C MRS measurements by comparing them with results from a standard biochemical assay. To
Validation of 13C NMR measurements of liver glycogen in vivo
โ Scribed by Rolf Gruetter; Inger Magnusson; Douglas L. Rothman; Malcolm J. Avison; Robert G. Shulman; Gerald I. Shulman
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 701 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
The natural abundance ^13^C NMR intensity of the glycogen C1 resonance was measured in the surgically exposed liver of rabbits in vivo (n = 17) by integration from 98 to 104 ppm and compared double blindedly to the subsequent biochemical measurement. Coil loading was measured each time from a reference sphere at the coil center and the NMR Intensity was normalized accordingly. For quantification, the normalized NMR intensity was calibrated using aqueous glycogen solutions ranging from 110 to 1100 ฮผmol glucosyl units/g (n = 14). An in vivo range from 110 to 800 pmol glucosyl unit/g wet weight was measured with a highly linear correlation with concentration (r = 0.85, P < 0.001). The in vivo NMR concentration was 0.95 ยฑ 0.05 (mean ยฑ standard error, n = 17) of the concomitant enzymatic measurement of glycogen content. We conclude that the ^13^C NMR signal of liver glycogen C1 is essentially 100% visible in vivo and that natural abundance ^13^C NMR spectroscopy can provide reliable noninvasive estimates of in vivo glycogen content over the physiological range of liver glycogen concentrations when using adequate localization and Integration procedures.
๐ SIMILAR VOLUMES
## Abstract The integrated ^13^C NMR intensity of the glycogen Cl resonance was measured in skeletal muscle (biceps femoris region) of nine rabbits under __in vivo__ conditions. Concurrent chemical determinations of glycogen content showed that the __in vivo__ signal was 1.02 ยฑ 0.06 the intensity o
## Abstract Recent developments in ^13^C nuclear magnetic resonance (NMR) spectroscopy have permitted noninvasive assessment of glycogen concentration in human skeletal muscle. Before these indirect measurements could be accepted as accurate, it was essential that validation should be carried out b