AJDRAJNR - American Journal of Neuroradiology

This Article
Right arrow Abstract Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Engelhorn, T.
Right arrow Articles by Hufnagel, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Engelhorn, T.
Right arrow Articles by Hufnagel, A.

Cerebral Perfusion Alterations during the Acute Phase of Experimental Generalized Status Epilepticus: Prediction of Survival By Using Perfusion-Weighted MR Imaging and Histopathology

T. Engelhorna, A. Doerflera, J. Weisec, M. Baehrc, M. Forstinga and A. Hufnagelb

a Department of Neuroradiology, University of Essen, Essen, Germany
b Department of Neurology, University of Essen, Essen, Germany
c Department of Neurology, University of Goettingen, Goettingen, Germany



View larger version (96K):

[in a new window]
 
FIG 1. Regions of interest used for quantitative analysis. A, Representative MR image on which regions of interest are outlined. B, Schematic drawing of a rat brain at similar level with identical regions of interest superimposed. regions of interest were defined as: retrosplenial parietal and temporal cortex (RCp and RCt), piriform cortex (PC), hippocampus (Hippo), thalamus (Thal), and amygdala (Amy).



View larger version (14K):

[in a new window]
 
FIG 2. Averaged BPRs in the retrosplenial parietal cortex of pilocarpine-treated animals at baseline conditions and at 3, 15, 30, 60, and 120 minutes after pilocarpin-induced SE, respectively. An asterisk denotes significant decease compared with baseline conditions. A double asterisk denotes significant increase compared with baseline conditions.



View larger version (14K):

[in a new window]
 
FIG 3. Averaged BPRs in the retrosplenial temporal cortex of pilocarpine -treated animals at baseline conditions and at 3, 15, 30, 60, and 120 minutes after pilocarpin-induced SE, respectively. An asterisk denotes significant decease compared with baseline conditions. A double asterisk denotes significant increase compared with baseline conditions.



View larger version (14K):

[in a new window]
 
FIG 4. Averaged BPRs in the piriform cortex of pilocarpine-treated animals at baseline conditions and at 3, 15, 30, 60, and 120 minutes after pilocarpin-induced SE, respectively. An asterisk denotes significant decease compared with baseline conditions. A double asterisk denotes significant increase compared with baseline conditions.



View larger version (13K):

[in a new window]
 
FIG 5. Averaged BPRs in the thalamus of pilocarpine-treated animals at baseline conditions and at 3, 15, 30, 60, and 120 minutes after pilocarpin-induced SE, respectively. An asterisk denotes significant decease compared with baseline conditions.



View larger version (14K):

[in a new window]
 
FIG 6. Averaged BPRs in the amygdala of pilocarpine-treated animals at baseline conditions and at 3, 15, 30, 60, and 120 minutes after pilocarpin-induced SE, respectively. An asterisk denotes significant decease compared with baseline conditions. A double asterisk denotes significant increase compared with baseline conditions.



View larger version (14K):

[in a new window]
 
FIG 7. Averaged BPRs in the hippocampus of pilocarpine-treated animals at baseline conditions and at 3, 15, 30, 60, and 120 minutes after pilocarpin-induced SE, respectively. An asterisk denotes significant decease compared with baseline conditions. A double asterisk denotes significant increase compared with baseline conditions.