Interpretation of BOLD MRI Signals in Rat Brain Using Simultaneously Measured Near‐Infrared Spectrophotometric Information

The purpose of this paper is to investigate the origin of the signal changes in the blood oxygenation level dependent effect (BOLD) and the influence of oxygen metabolism by utilizing near‐infrared spectrophotometry (NIRS), which can measure deoxyhemoglobin (deoxyHb) content in blood vessels and redox states of cytochrome oxidase in whole tissue. Simultaneous MRI and NIRS measurements of the rat head were performed by changing oxygen concentrations in the inhalant gas. The signal intensity based on the BOLD effect depended on the influence of both arterial and venous blood deoxygenation in the brain, whose relative contributions differed at various points. In this paper, it is noteworthy that the differential apparent transverse relaxation rate between two conditions in the brain areas was linearly correlated with deoxyHb content determined by NIRS, except in severe hypoxia, and that no reduction of cytochrome oxidase occurred under the same conditions. These results indicate that the influence of hemodynamic changes on the signal intensity of the BOLD effect, and therefore functional MRI, can be elucidated by the NIRS information to determine actual changes of blood deoxygenation and blood volume.

[1]  F. Jöbsis Noninvasive, infrared monitoring of cerebral and myocardial oxygen sufficiency and circulatory parameters. , 1977, Science.

[2]  D. W. Alderman,et al.  An efficient decoupler coil design which reduces heating in conductive samples in superconducting spectrometers , 1979 .

[3]  I. Yamazaki,et al.  The Effect of Intracellular Oxygen Concentration on Lactate Release, Pyridine Nucleotide Reduction, and Respiration Rate in the Rat Cardiac Tissue , 1983, Circulation research.

[4]  M. Tamura,et al.  Quantitative analysis of hemoglobin oxygenation state of rat brain in situ by near-infrared spectrophotometry. , 1988, Journal of applied physiology.

[5]  Near infrared quadruple wavelength spectrophotometry of the rat head. , 1989, Advances in experimental medicine and biology.

[6]  S. Ogawa,et al.  Oxygenation‐sensitive contrast in magnetic resonance image of rodent brain at high magnetic fields , 1990, Magnetic resonance in medicine.

[7]  R. Shulman,et al.  Lactate rise detected by 1H NMR in human visual cortex during physiologic stimulation. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[8]  R. Turner,et al.  Echo‐planar time course MRI of cat brain oxygenation changes , 1991, Magnetic resonance in medicine.

[9]  R. Turner,et al.  Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[10]  Ravi S. Menon,et al.  Intrinsic signal changes accompanying sensory stimulation: functional brain mapping with magnetic resonance imaging. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[11]  A. P. Georgopoulos,et al.  Functional magnetic resonance imaging of motor cortex: hemispheric asymmetry and handedness. , 1993, Science.

[12]  S. Ogawa,et al.  The sensitivity of magnetic resonance image signals of a rat brain to changes in the cerebral venous blood oxygenation , 1993, Magnetic resonance in medicine.

[13]  J. Frahm,et al.  Functional MRI of human brain activation at high spatial resolution , 1993, Magnetic resonance in medicine.

[14]  Yoko Hoshi,et al.  Dynamic changes in cerebral oxygenation in chemically induced seizures in rats: study by near-infrared spectrophotometry , 1993, Brain Research.

[15]  J. Frahm,et al.  Cerebral blood oxygenation in rat brain during hypoxic hypoxia. Quantitative MRI of effective transverse relaxation rates , 1994, Magnetic resonance in medicine.

[16]  R S Balaban,et al.  Comparison of EPI gradient‐echo contrast changes in cat brain caused by respiratory challenges with direct simultaneous evaluation of cerebral oxygenation via a cranial window , 1994, NMR in biomedicine.

[17]  S. Ogawa,et al.  BOLD Based Functional MRI at 4 Tesla Includes a Capillary Bed Contribution: Echo‐Planar Imaging Correlates with Previous Optical Imaging Using Intrinsic Signals , 1995, Magnetic resonance in medicine.

[18]  Y Hoshi,et al.  Near-infrared monitoring of cerebral oxygenation state during carotid endarterectomy. , 1996, Surgical neurology.