BOLD and CBV-weighted functional magnetic resonance imaging of the rat somatosensory system

A multislice spin echo EPI sequence was used to obtain functional MR images of the entire rat brain with blood oxygenation level dependent (BOLD) and cerebral blood volume (CBV) contrast at 11.7 T. Maps of activation incidence were created by warping each image to the Paxinos rat brain atlas and mar...

Full description

Saved in:
Bibliographic Details
Published inMagnetic resonance in medicine Vol. 55; no. 2; pp. 316 - 324
Main Authors Keilholz, Shella D., Silva, Afonso C., Raman, Mira, Merkle, Hellmut, Koretsky, Alan P.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.02.2006
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:A multislice spin echo EPI sequence was used to obtain functional MR images of the entire rat brain with blood oxygenation level dependent (BOLD) and cerebral blood volume (CBV) contrast at 11.7 T. Maps of activation incidence were created by warping each image to the Paxinos rat brain atlas and marking the extent of the activated area. Incidence maps for BOLD and CBV were similar, but activation in draining veins was more prominent in the BOLD images than in the CBV images. Cerebellar activation was observed along the surface in BOLD images, but in deeper regions in the CBV images. Both effects may be explained by increased signal dropout and distortion in the EPI images after administration of the ferumoxtran‐10 contrast agent for CBV fMRI. CBV‐weighted incidence maps were also created for 10, 20, and 30 mg Fe/kg doses of ferumoxtran‐10. The magnitude of the average percentage change during stimulation increased from 4.9% with the 10 mg Fe/kg dose to 8.7% with the 30‐mg Fe/kg dose. Incidence of activation followed a similar trend. Magn Reson Med, 2006. Published 2005 Wiley‐Liss, Inc.
Bibliography:ark:/67375/WNG-K2K6M2W3-6
istex:591F5E7DB649AA1827626242AE07964CACFD60C1
ArticleID:MRM20744
NIH, NINDS intramural research program
This article is a US Government work and, as such, is in the public domain in the United States of America.
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.20744