Abstract |
In hyperpolarized xenon magnetic resonance imaging ( HP (129)Xe MRI), the inhaled spin-1/2 isotope of xenon gas is used to generate the MR signal. Because hyperpolarized xenon is an MR signal source with properties very different from those generated from water- protons, HP (129)Xe MRI may yield structural and functional information not detectable by conventional proton-based MRI methods. Here we demonstrate the differential distribution of HP (129)Xe in the cerebral cortex of the rat following a pain stimulus evoked in the animal's forepaw. Areas of higher HP (129)Xe signal corresponded to those areas previously demonstrated by conventional functional MRI (fMRI) methods as being activated by a forepaw pain stimulus. The percent increase in HP (129)Xe signal over baseline was 13-28%, and was detectable with a single set of pre and post stimulus images. Recent innovations in the production of highly polarized (129)Xe should make feasible the emergence of HP (129)Xe MRI as a viable adjunct method to conventional MRI for the study of brain function and disease.
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Authors | Mary L Mazzanti, Ronn P Walvick, Xin Zhou, Yanping Sun, Niral Shah, Joey Mansour, Jessica Gereige, Mitchell S Albert |
Journal | PloS one
(PLoS One)
Vol. 6
Issue 7
Pg. e21607
( 2011)
ISSN: 1932-6203 [Electronic] United States |
PMID | 21789173
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Animals
- Brain
(drug effects, metabolism)
- Brain Mapping
- Magnetic Resonance Imaging
- Male
- Physical Stimulation
- Rats
- Rats, Sprague-Dawley
- Sensation
(drug effects)
- Xenon
(administration & dosage, pharmacokinetics, pharmacology)
- Xenon Isotopes
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