## Abstract An inversion‐recovery pulse sequence and solenoidal surface coil were employed to determine the spin‐lattice relaxation time (T1) in murine tumors (RIF‐1 and SCCVII). Reduction in T1s of inorganic phosphate (P~i~) and nucleotide triphosphates (NTP) has been observed in irradiated tumors
Localized proton spectroscopy of focal brain pathology in humans: Significant effects of edema on spin–spin relaxation time
✍ Scribed by Kyousuke Kamada; Kiyohiro Houkin; Kazutoshi Hida; Hitoshi Matsuzawa; Yoshinobu Iwasaki; Hiroshi Abe; Tsutomu Nakada
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 392 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Localized proton nuclear magnetic resonance (NMR) spectroscopy of human brain in two common focal pathologies producing brain edema (peritumor edema and acute edema–tous ischemic stroke) was performed utilizing point resolved spectroscopy (PRESS). The spectra obtained from the pathological tissues were characterized by a reduced N‐acetyl‐as–partate (NAA) to total creatine (Cr) ratio (NAA/Cr) and high level of lactate. While the spin lattice relaxation time (T~1~) of the main metabolite resonances, namely, those of NAA, Cr, and choline containing compounds (Cho), showed values similar to those of normal brain, the spin‐spin relaxation time (T~2~) of these metabolites exhibited a dramatic shortening in pathological tissues. Serial postoperative measurements of T~2~ in two patients with peritumor edema showed a gradual recovery of the T~2~ shortening corresponding to improvement of the edema. The majority of localized spectroscopy studies in humans is performed using a sequence which utilizes spin echo signals with a fixed single echo time. Hence, the signal intensities of the metabolite resonances obtained are inherently T~2~ dependent. The current study underscores that cautious interpretation of clinical data with respect to metabolite quantification is warranted.
📜 SIMILAR VOLUMES
## Experimental and clinical studies have led to the hypothesis The liver is the primary site of oxidative metabolism in humans. Ingestion of ethanol and drugs such as phenobarbi-that the phosphodiester signal obtained by 31 P magnetic resonance (MR) spectroscopy may be a specific marker for the