Changes of glucose metabolism in mouse models of intracerebral hemorrhage：18 F-FDG microPET/CT study
10.3760/cma.j.issn.2095-2848.2015.06.015
- VernacularTitle:小鼠脑出血后脑葡萄糖代谢变化的18 F-FDG micro PET／CT显像研究
- Author:
Fanhui YANG
;
Qin WANG
;
Chunyin ZHANG
;
Hua TAN
;
Chaoxian YANG
;
Wei WANG
;
Qiang YOU
- Publication Type:Journal Article
- Keywords:
Cerebral hemorrhage;
Tomography,emission-computed;
Tomography,X-ray computed;
Deoxyglucose;
Mice
- From:
Chinese Journal of Nuclear Medicine and Molecular Imaging
2015;(6):483-486
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the brain glucose metabolism with 18 F?FDG microPET/CT in mouse models of intracerebral hemorrhage (ICH). Methods A total of 12 healthy adult male mice were randomly divided into sham operation group (group A, n=6) and ICH model group (group B, n=6) by simple random sampling method. The animal models were established by injecting collagenase Ⅳ into the caudate nucleus of mice. Thereafter (5.5±0.3) MBq of 18F?FDG was injected into caudal vein at 6 h, 24 h, 48 h and 3 d, 5 d, 8 d, 14 d, respectively, following anesthesia. 18 F?FDG microPET/CT scans were ac?quired 30 min after the trace injection. SUV in the perihematomal brain tissue of ICH was measured and an?alyzed. Two?sample t test was used to compare SUV between groups. Results ( 1) Some mice had mild neurologic deficit after the sham operation in group A, while all mice had a marked neurologic deficit in group B, especially at 24 h after 18 F?FDG injection. ( 2) After 6 h, FDG uptake in perihematomal brain tis?sue decreased(SUV=0.80±0.04), which significantly lower than that in the opposite side(SUV=1.10± 0?04;t=2.69, P<0.05) and decreased to the minimum at 24 h(SUV=0.50±0.05). 18F?FDG uptake in perihematomal brain tissue began to increase at 3 d(SUV=1.20±0.05) and kept increasing during the 14 d observation. Compared with the group A, glucose metabolism in group B was significantly lower at each time point(t=37.67-86.60, all P<0.05). Conclusions 18 F?FDG microPET/CT may dynamically reflect the changes of brain glucose metabolism in ICH mouse models. The FDG uptake in the center of ICH may disap?pear and the volume of hematoma with decreased uptake may shrink during the observation period.
