» Articles » PMID: 8386018

Functional Brain Mapping by Blood Oxygenation Level-dependent Contrast Magnetic Resonance Imaging. A Comparison of Signal Characteristics with a Biophysical Model

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1993 Mar 1
PMID 8386018
Citations 478
Authors
Affiliations
Soon will be listed here.
Abstract

It recently has been demonstrated that magnetic resonance imaging can be used to map changes in brain hemodynamics produced by human mental operations. One method under development relies on blood oxygenation level-dependent (BOLD) contrast: a change in the signal strength of brain water protons produced by the paramagnetic effects of venous blood deoxyhemoglobin. Here we discuss the basic quantitative features of the observed BOLD-based signal changes, including the signal amplitude and its magnetic field dependence and dynamic effects such as a pronounced oscillatory pattern that is induced in the signal from primary visual cortex during photic stimulation experiments. The observed features are compared with the results of Monte Carlo simulations of water proton intravoxel phase dispersion produced by local field gradients generated by paramagnetic deoxyhemoglobin in nearby venous blood vessels. The simulations suggest that the effect of water molecule diffusion is strong for the case of blood capillaries, but, for larger venous blood vessels, water diffusion is not an important determinant of deoxyhemoglobin-induced signal dephasing. We provide an expression for the apparent in-plane relaxation rate constant (R2*) in terms of the main magnetic field strength, the degree of the oxygenation of the venous blood, the venous blood volume fraction in the tissue, and the size of the blood vessel.

Citing Articles

Brain networks in newborns and infants with and without sensorineural hearing loss: A functional near-infrared spectroscopy study.

Tan J, Hou Q, Zhang F, Duan X, Zhang Y, Lee Y World J Psychiatry. 2024; 14(10):1547-1557.

PMID: 39474384 PMC: 11514573. DOI: 10.5498/wjp.v14.i10.1547.


Denoising task-correlated head motion from motor-task fMRI data with multi-echo ICA.

Reddy N, Zvolanek K, Moia S, Caballero-Gaudes C, Bright M Imaging Neurosci (Camb). 2024; 2.

PMID: 39328846 PMC: 11426116. DOI: 10.1162/imag_a_00057.


Identification of potential inhibitors for drug-resistant EGFR mutations in non-small cell lung cancer using whole exome sequencing data.

Nagarajan N, Guda C Front Pharmacol. 2024; 15:1428158.

PMID: 39130636 PMC: 11310931. DOI: 10.3389/fphar.2024.1428158.


Multivariate pattern analysis of medical imaging-based Alzheimer's disease.

Alarjani M, Almarri B Front Med (Lausanne). 2024; 11:1412592.

PMID: 39099597 PMC: 11294205. DOI: 10.3389/fmed.2024.1412592.


Mitigation of Fetal Radiation Injury from Mid-Gestation Total-body Irradiation by Maternal Administration of Mitochondrial-Targeted GS-Nitroxide JP4-039.

Wu Y, Christodoulou A, Beumer J, Rigatti L, Fisher R, Ross M Radiat Res. 2024; 202(3):565-579.

PMID: 39074819 PMC: 11552446. DOI: 10.1667/RADE-24-00095.1.


References
1.
Frahm J, Bruhn H, Merboldt K, Hanicke W . Dynamic MR imaging of human brain oxygenation during rest and photic stimulation. J Magn Reson Imaging. 1992; 2(5):501-5. DOI: 10.1002/jmri.1880020505. View

2.
Fox P, Raichle M, Mintun M, Dence C . Nonoxidative glucose consumption during focal physiologic neural activity. Science. 1988; 241(4864):462-4. DOI: 10.1126/science.3260686. View

3.
Kwong K, Belliveau J, Chesler D, Goldberg I, Weisskoff R, Poncelet B . Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation. Proc Natl Acad Sci U S A. 1992; 89(12):5675-9. PMC: 49355. DOI: 10.1073/pnas.89.12.5675. View

4.
Le Bihan D, Turner R . Intravoxel incoherent motion imaging using spin echoes. Magn Reson Med. 1991; 19(2):221-7. DOI: 10.1002/mrm.1910190206. View

5.
Haglund M, Ojemann G, Hochman D . Optical imaging of epileptiform and functional activity in human cerebral cortex. Nature. 1992; 358(6388):668-71. DOI: 10.1038/358668a0. View