IP NMR spin-lattice (TI) and spin-spin (T2) relaxation times of phosphocreatine, ATP, inorganic phosphate, and phosphomonoesters have been measured in vivo at 4.1 T in rat brain and rat brain tumors implanted on nude mice. The relaxation data were acquired using a phase-cycled saturation-recovery sp
Method to determine in vivo the relaxation time T1 of hyperpolarized xenon in rat brain
✍ Scribed by Philippe Choquet; Jean-Noël Hyacinthe; Guillaume Duhamel; Emmanuelle Grillon; Jean-Louis Leviel; André Constantinesco; Anne Ziegler
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 130 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The magnetic polarization of the stable ^129^Xe isotope may be enhanced dramatically by means of optical techniques and, in principle, hyperpolarized ^129^Xe MRI should allow quantitative mapping of cerebral blood flow with better spatial resolution than scintigraphic techniques. A parameter necessary for this quantitation, and not previously known, is the longitudinal relaxation time (T) of ^129^Xe in brain tissue in vivo: a method for determining this is reported. The time course of the MR signal in the brain during arterial injection of hyperpolarized ^129^Xe in a lipid emulsion was analyzed using an extended two‐compartment model. The model uses experimentally determined values of the RF flip angle and the T~1~ of ^129^Xe in the lipid emulsion. Measurements on rats, in vivo, at 2.35 T gave T = 3.6 ± 2.1 sec (±SD, n = 6). This method enables quantitative mapping of cerebral blood flow. Magn Reson Med 49:1014–1018, 2003. © 2003 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract On‐resonance longitudinal relaxation time in the rotating frame (__T__~1ρ~) has been shown to provide unique information during the early minutes of acute stroke. In the present study, the contributions of the different relaxation mechanisms to on‐resonance __T__~1ρ~ relaxation were ass
A single-voxel Carr-Purcell-Meibloom-Gill sequence was developed to measure localized T(2) relaxation times of (13)C-labeled metabolites in vivo for the first time. Following hyperpolarized [1-(13)C]pyruvate injections, pyruvate and its metabolic products, alanine and lactate, were observed in the l
19Fluorine NMRS has the potential to enable noninvasive predictions of tumor response to 5-fluorouracil (5FU) therapy based on tumor pharmacokinetics. Knowledge of the T1's of 5FU and its fluoronucleotide anabolites (FNuc) is required for quantitative spectral analysis and selection of optimal pulse
## Abstract ## Purpose To measure regional T1 and T2 values for normal C57Bl/6 mouse brain and changes in T1 after systemic administration of manganese chloride (MnCl~2~) at 9.4 T. ## Materials and Methods C57Bl/6 mice were anesthetized and baseline T1 and T2 measurements obtained prior to measu
## Abstract Knowledge of __T__~1~ relaxation times can be important for accurate relative and absolute quantification of brain metabolites, for sensitivity optimizations, for characterizing molecular dynamics, and for studying changes induced by various pathological conditions. ^1^H __T__~1~ relaxa