http://www.cnr.it/ontology/cnr/individuo/prodotto/ID313208
Statistical voxel-based analysis of [F-18]FDG PET animal studies for the estimation of glucose metabolism in stress conditions (Abstract/Poster in rivista)
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- Label
- Statistical voxel-based analysis of [F-18]FDG PET animal studies for the estimation of glucose metabolism in stress conditions (Abstract/Poster in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Alternative label
Di Grigoli, G.; Gallivanone, F.; Musazzi, L.; Gelsomino, G.; Treccani, G.; Valtorta, S.; Grosso, E.; Castiglioni, I.; Gilardi, M. C.; Popoli, M.; Moresco, R. M.; Fazio, F. (2012)
Statistical voxel-based analysis of [F-18]FDG PET animal studies for the estimation of glucose metabolism in stress conditions
(literal)
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- Di Grigoli, G.; Gallivanone, F.; Musazzi, L.; Gelsomino, G.; Treccani, G.; Valtorta, S.; Grosso, E.; Castiglioni, I.; Gilardi, M. C.; Popoli, M.; Moresco, R. M.; Fazio, F. (literal)
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- ISI Web of Science (WOS) (literal)
- Abstract (literal)
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- IBFM CNR; University of Milano-Bicocca; Vita-Salute San Raffaele University; University of Milan; University of Milano-Bicocca (literal)
- Titolo
- Statistical voxel-based analysis of [F-18]FDG PET animal studies for the estimation of glucose metabolism in stress conditions (literal)
- Abstract
- Aim: Aim of this study was to evaluate the effect of acute stress on rat brain metabolism using PET
[18F]FDG and Foot-Shock (FS) paradigm. Regional stress effect was evaluated both by a statistical voxelbased
analysis using a rat-model version of Statistical Parametric Mapping (SPM) optimized in our facility.
Materials & Methods: 16 male CD rats, randomly assigned into two groups, 8 rats for Control Group (CG)
and 8 rats for Stressed Group (SG), were injected with [18F]FDG in a lateral tail vein. Following the FS
protocol, the SG was exposed, immediately after radiotracer injection, to the shock session. One hour after
[18F]FDG injection, CG and SG were then subjected to a PET brain study for 30 minutes. All animals have
been then sacrificed and corticosterone and circulating glucose were measured. A rat template was created
using a control rat, outside of the two groups, who performed, in addition to the PET study, an and MRI
study: the PET images for this rat, co-registered to his MRI, was used as [18F]FDG/MRI template. Statistical
analysis were performed setting p<0.05, a threshold of 100 voxels and rescaling data to a mean glucose
consumption value of 28mol/100g/min. In particular three SPM design were used: 1) a single subject design
was used both to perform a Jack-Knife analysis on CG and to evaluate each SG rat with respect to CG; 2) a
compare-populations model was used to evaluate differences in SG with respect to CG; 3) a simple
regression model allowed to evaluate correlations between cerebral glucose metabolism and corticosterone
levels in different brain regions.
Results: Jack-Knife analysis on CG showed that one rat had a pattern of altered metabolism in comparison
to the other control rats, suggesting a different susceptibility to experimental handling. This rat was excluded
from analysis. Single-subject analysis on stressed rats revealed a similar pattern, except for one animal.
Interestingly this rat escaped from box during stress paradigm. Group analysis showed a relative reduction of
regional brain metabolism at the level of thalamus, hypothalamus, entorhinal and piriform cortex, and
cerebellum, while an increase was observed in motor, somato-sensory cortex, olfactory bulb regions and
hippocampal subregions. A negative correlation was observed between cerebral glucose metabolism and
corticosterone levels in different brain regions.
Conclusion: Results of the study indicated that acute stress modifies regional brain functions and these
modifications are associated with circulating level of stress markers like corticosterone. (literal)
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