Literature DB >> 12030817

Repeated fMRI using iron oxide contrast agent in awake, behaving macaques at 3 Tesla.

Francisca P Leite1, Doris Tsao, Wim Vanduffel, Denis Fize, Yuka Sasaki, Larry L Wald, Anders M Dale, Ken K Kwong, Guy A Orban, Bruce R Rosen, Roger B H Tootell, Joseph B Mandeville.   

Abstract

Iron oxide contrast agents have been employed extensively in anesthetized rodents to enhance fMRI sensitivity and to study the physiology of cerebral blood volume (CBV) in relation to blood oxygen level-dependent (BOLD) signal following neuronal activation. This study quantified the advantages of exogenous agent for repeated neuroimaging in awake, nonhuman primates using a clinical 3 Tesla scanner. A monocrystalline iron oxide nanoparticle (MION) solution was injected at iron doses of 8 to 10 mg/kg in two macaque monkeys. Adverse behavioral effects due to contrast agent were not observed in either monkey using cumulative doses in excess of 60 mg/kg. Relative to BOLD imaging at 3 Tesla, MION increased functional sensitivity by an average factor of 3 across the brain for a stimulus of long duration. Rapid stimulus presentation attenuated MION signal changes more than BOLD signal changes, due to the slower time constant of the blood volume response relative to BOLD signal. Overall, the contrast agent produced a dramatic improvement in functional brain imaging results in the awake, behaving primate at this field strength. (c) 2002 Elsevier Science (USA).

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Year:  2002        PMID: 12030817     DOI: 10.1006/nimg.2002.1110

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  109 in total

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5.  Facial Expressions Evoke Differential Neural Coupling in Macaques.

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Review 7.  IRON fMRI measurements of CBV and implications for BOLD signal.

Authors:  Joseph B Mandeville
Journal:  Neuroimage       Date:  2012-01-16       Impact factor: 6.556

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9.  An anterior temporal face patch in human cortex, predicted by macaque maps.

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10.  Evaluation of MRI models in the measurement of CMRO2 and its relationship with CBF.

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