Changes of cerebral blood oxygenation and optical pathlength during activation and deactivation in the prefrontal cortex measured by time-resolved near infrared spectroscopy.

To determine the alterations in optical characteristics and cerebral blood oxygenation (CBO) during activation and deactivation, we evaluated the changes in mean optical pathlength (MOP) and CBO induced by a verbal fluency task (VFT) and driving simulation in the right and left prefrontal cortex (PFC), employing a newly developed time-resolved near infrared spectroscopy, which allows quantitative measurements of the evoked-CBO changes by determining the MOP with a sampling time of 1 s. The results demonstrated differences in MOP in the foreheads with the subjects and wavelength; however, there was no significant difference between the right and left foreheads (p > 0.05). Also, both the VFT and driving simulation task did not affect the MOP significantly as compared to that before the tasks (p > 0.05). In the bilateral PFCs, the VFT caused increases of oxyhemoglobin and total hemoglobin associated with a decrease of deoxyhemoglobin, while the driving simulation task caused decreases of oxyhemoglobin and total hemoglobin associated with an increase of deoxyhemoglobin; there were no significant differences in evoked-CBO changes between the right and left PFC. The present results will be useful for quantitative measurement of hemodynamic changes during activation and deactivation in the adults by near infrared spectroscopy.

[1]  M. Herrmann,et al.  Frontal activation during a verbal-fluency task as measured by near-infrared spectroscopy , 2003, Brain Research Bulletin.

[2]  E. Gratton,et al.  Fast cerebral functional signal in the 100-ms range detected in the visual cortex by frequency-domain near-infrared spectrophotometry. , 2003, Psychophysiology.

[3]  A. Kleinschmidt,et al.  Simultaneous Recording of Cerebral Blood Oxygenation Changes during Human Brain Activation by Magnetic Resonance Imaging and Near-Infrared Spectroscopy , 1996, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[4]  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.

[5]  Michael Erb,et al.  Brain areas activated in fMRI during self-regulation of slow cortical potentials (SCPs) , 2003, Experimental Brain Research.

[6]  S. Arridge,et al.  Estimation of optical pathlength through tissue from direct time of flight measurement , 1988 .

[7]  Y. Katayama,et al.  Increase in focal concentration of deoxyhaemoglobin during neuronal activity in cerebral ischaemic patients , 2002, Journal of neurology, neurosurgery, and psychiatry.

[8]  G L Shulman,et al.  INAUGURAL ARTICLE by a Recently Elected Academy Member:A default mode of brain function , 2001 .

[9]  Henrik Walter,et al.  The neural correlates of driving , 2001, Neuroreport.

[10]  A. Villringer,et al.  Cerebral haemoglobin oxygenation during sustained visual stimulation--a near-infrared spectroscopy study. , 1997, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[11]  J. Pekar,et al.  Erratum: Different activation dynamics in multiple neural systems during simulated driving (Human Brain Mapping (2002) 16 (158-167)) , 2002 .

[12]  Huijuan Zhao,et al.  Maps of optical differential pathlength factor of human adult forehead, somatosensory motor and occipital regions at multi-wavelengths in NIR. , 2002, Physics in medicine and biology.

[13]  Y. Katayama,et al.  Decreases of blood oxygenation level--dependent signal in the activated motor cortex during functional recovery after resection of a glioma. , 2004, AJNR. American journal of neuroradiology.

[14]  B. Wilson,et al.  Time resolved reflectance and transmittance for the non-invasive measurement of tissue optical properties. , 1989, Applied optics.

[15]  L. Skov,et al.  Carbon Dioxide-Related Changes in Cerebral Blood Volume and Cerebral Blood Flow in Mechanically Ventilated Preterm Neonates: Comparison of Near Infrared Spectrophotometry and 133Xenon Clearance , 1990, Pediatric Research.

[16]  D. Delpy,et al.  Optical pathlength measurements on adult head, calf and forearm and the head of the newborn infant using phase resolved optical spectroscopy. , 1995, Physics in medicine and biology.

[17]  A. Grinvald,et al.  Interactions Between Electrical Activity and Cortical Microcirculation Revealed by Imaging Spectroscopy: Implications for Functional Brain Mapping , 1996, Science.

[18]  Neuronal activity alters local blood flow in brain tumour adjacent to the activating cortex , 1999, Journal of neurology, neurosurgery, and psychiatry.

[19]  D. Tank,et al.  Brain magnetic resonance imaging with contrast dependent on blood oxygenation. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[20]  J. Pekar,et al.  Different activation dynamics in multiple neural systems during simulated driving , 2002, Human brain mapping.

[21]  G. Krüger,et al.  MRI of Functional Deactivation: Temporal and Spatial Characteristics of Oxygenation-Sensitive Responses in Human Visual Cortex , 1999, NeuroImage.

[22]  Y. Hoshi Functional near-infrared optical imaging: utility and limitations in human brain mapping. , 2003, Psychophysiology.

[23]  Stephen M. Rao,et al.  Human Brain Language Areas Identified by Functional Magnetic Resonance Imaging , 1997, The Journal of Neuroscience.

[24]  M. Raichle,et al.  Focal physiological uncoupling of cerebral blood flow and oxidative metabolism during somatosensory stimulation in human subjects. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[25]  K. Sakatani,et al.  Language-activated cerebral blood oxygenation and hemodynamic changes of the left prefrontal cortex in poststroke aphasic patients: a near-infrared spectroscopy study. , 1998, Stroke.

[26]  Janette Atkinson,et al.  Regional Hemodynamic Responses to Visual Stimulation in Awake Infants , 1998, Pediatric Research.

[27]  S. Takashima,et al.  Human Visual Cortical Function during Photic Stimulation Monitoring by Means of near-Infrared Spectroscopy , 1993, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[28]  Yutaka Tsuchiya,et al.  Simple Subtraction Method for Determining the Mean Path Length Traveled by Photons in Turbid Media , 1998 .

[29]  W. Strik,et al.  Loss of functional hemispheric asymmetry in Alzheimer's dementia assessed with near-infrared spectroscopy. , 1997 .

[30]  K. Sakatani,et al.  Cerebral blood oxygenation changes induced by auditory stimulation in newborn infants measured by near infrared spectroscopy. , 1999, Early human development.

[31]  Dae-Shik Kim,et al.  Origin of Negative Blood Oxygenation Level—Dependent fMRI Signals , 2002, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[32]  Y. Katayama,et al.  Changes in cerebral blood oxygenation of the frontal lobe induced by direct electrical stimulation of thalamus and globus pallidus: a near infrared spectroscopy study , 1999, Journal of neurology, neurosurgery, and psychiatry.

[33]  K. Sakatani,et al.  Effects of aging on language-activated cerebral blood oxygenation changes of the left prefrontal cortex: Near infrared spectroscopy study. , 1999, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

[34]  E. Mohr,et al.  Neuropsychological Assessment. Third Edition , 1996 .

[35]  M. Tamura,et al.  Detection of dynamic changes in cerebral oxygenation coupled to neuronal function during mental work in man , 1993, Neuroscience Letters.

[36]  藤原 徳生,et al.  Evoked-cerebral blood oxygenation changes in false-negative activations in BOLD contrast functional MRI of patients with brain tumors , 2005 .

[37]  M. Cope,et al.  New non-invasive methods for assessing brain oxygenation and haemodynamics. , 1988, British medical bulletin.

[38]  Alessandro Torricelli,et al.  Bilateral prefrontal cortex oxygenation responses to a verbal fluency task: a multichannel time-resolved near-infrared topography study. , 2005, Journal of biomedical optics.

[39]  Monica Fabiani,et al.  The event-related optical signal (EROS) in visual cortex: replicability, consistency, localization, and resolution. , 2003, Psychophysiology.

[40]  M. Tamura,et al.  Interpretation of near-infrared spectroscopy signals: a study with a newly developed perfused rat brain model. , 2001, Journal of applied physiology.

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

[42]  D F Hanley,et al.  Effects of graded hypotension on cerebral blood flow, blood volume, and mean transit time in dogs. , 1992, The American journal of physiology.

[43]  Egill Rostrup,et al.  Change of visually induced cortical activation patterns during development , 1996, The Lancet.

[44]  M. Tanida,et al.  Relation between asymmetry of prefrontal cortex activities and the autonomic nervous system during a mental arithmetic task: near infrared spectroscopy study , 2004, Neuroscience Letters.

[45]  D. Loewenstein,et al.  Cerebral metabolic effects of a verbal fluency test: a PET scan study. , 1988, Journal of clinical and experimental neuropsychology.

[46]  M. Lezak Neuropsychological assessment, 3rd ed. , 1995 .

[47]  Ulrich Dirnagl,et al.  Age Dependency of Changes in Cerebral Hemoglobin Oxygenation during Brain Activation: A Near-Infrared Spectroscopy Study , 1995, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.