TABLE 1.
Imaging modality |
Method | Measurement | Advantages | Disadvantages |
---|---|---|---|---|
HUMAN STUDIES | ||||
PET | Measures emissions from radiolabeled chemical injected into the bloodstream |
H2O15 – blood flow F18 Fluorodeoxyglucose (FDG) – cellular metabolism |
• Can directly show blood flow (H2O15) or glucose metabolism (FDG) in brain tissues |
• Variable temporal resolution (tracer dependent) • Radiation exposure |
PET ligand | Radiolabeled drug/molecule of interest |
• Can observe regional receptor occupancy | • Ligand availability • Radiation exposure |
|
fMRI | Measures magnetic variations due to the amount of oxygenated and deoxygenated hemoglobin |
Blood oxygen level dependence (BOLD), which correlates with blood flow |
• Noninvasive • Good spatial resolution • Good temporal resolution |
• BOLD is an indirect measure of blood flow • Some regions of the brain are poorly visualized due to technical artifacts |
ANIMAL STUDIES | ||||
fMRI | Measures magnetic variations due to the amount of oxygenated and deoxygenated hemoglobin |
Blood oxygen level dependence (BOLD), which correlates with blood flow |
• Good spatial and temporal resolution • Able to accommodate repeated studies in a single animal |
• Requires sedation and restraint of the animal to avoid movement |
microPET | Measures emissions from radiolabeled tracers injected into the bloodstream |
H2O15 – blood flow 18F Fluorodeoxyglucose (FDG) – cellular metabolism |
• Uptake of radiotracer may take place in ambulatory animals (FDG) • Able to accommodate repeated studies in a single animal |
• Poor spatial resolution for brain imaging in small animals • Requires sedation and restraint of the animal to avoid movement |
c-fos | Evaluates early response genes |
c-fos mRNA or protein | • Spatial resolution at the cellular level | • Poor temporal resolution • Poor ability for 3D mapping • Requires animal sacrifice so repeated studies cannot be performed |
Autoradiography | Injection of radiotracer and exposure of the cryosectioned brain to photographic film or a phosphor imager |
Cerebral blood flow, Cerebral metabolism |
• Good spatial and temporal resolution • Imaging in nonrestrained, nonsedated animals |
• Requires animal sacrifice so repeated studies cannot be performed. |