In positron emission tomography (PET) studies of diseased animals, it is ve
ry useful to have accurate anatomical information as a reference. In human
studies, anatomical information is usually obtained from magnetic resonance
imaging (MRI) of the subject with retrospective registration of the subjec
t's PET image to the MRI. A number of PET-MRI registration techniques are u
sed for this purpose. However, the utility of these methods has not been te
sted for animals image registration. This paper studies the feasibility of
applying two currently used human brain PET-MRI registration techniques to
cat brain images. Methods: Three cats were anesthetized with isoflurane gas
, and PET images were acquired with (H2O)-O-15, benzodiazepine receptor lig
and C-11-flumazemil (FMZ), dopamine receptor ligand C-11-nemonapride (NEM)
and fluorodeoxy glucose (F-18-FDG). The four PET scans were acquired consec
utively within the same day while the cat remained fixed in the scanner. We
also obtained T1-weighted and T2-weighted MRI of the cats in a 4.7 T unit.
The PET images were registered to MRI using two human brain registration t
echniques: a semi-automatic method (SAM), which is a two-step method based
on the extraction of the midsagittal plane, and an automatic method (AMIR)
method that minimizes PET pixel variance within spatially connected segment
s determined by MRI. Results: T2-weighted MRI provided better structural in
formation than T1, MRI. FMZ did, while FDG or H2O PET images did not, provi
de a structural outline of the brain. The FMZ PET image was registered to M
RI satisfactorily using SAM. The striatum visualized in nemonapride PET ima
ge re-sliced with the same parameters matched the striatum identified in T2
-weighted MRI. Registration by AMIR was successful by inspection for FMZ, F
DG or H2O PET images in only one of the three cats. The registration error
of SAM was estimated to be less than 2 mm or 2 degrees. Conclusion: A satis
factory registration of FMZ-PET to T2-weighted MRI of the cat brain was obt
ained by a two-step manual registration technique. This will enhance the us
efulness of PET in the field of cerebral pathophysiology. (C) 2000 Publishe
d by Elsevier Science B.V. All rights reserved.