Skip to main content
Philosophical Transactions of the Royal Society B: Biological Sciences logoLink to Philosophical Transactions of the Royal Society B: Biological Sciences
. 1997 Jun 29;352(1354):737–742. doi: 10.1098/rstb.1997.0056

Localized near-infrared spectroscopy and functional optical imaging of brain activity.

M Tamura 1, Y Hoshi 1, F Okada 1
PMCID: PMC1691956  PMID: 9232862

Abstract

Changes in cerebral blood flow (CBF) and cerebral metabolic rates (CMRO2) have been used as indices for changes in neuronal activity. Near-infrared spectroscopy (NIRS) can also measure cerebral haemodynamics and metabolic changes, enabling the possible use of multichannel recording of NIRS for functional optical imaging of human brain activity. Spatio-temporal variations of brain regions were demonstrated during various mental tasks. Non-synchronous behaviour of cerebral haemodynamics during the neuronal activation was observed. Gender- and handedness-dependent lateralization of the function between right and left hemispheres was demonstrated by simultaneous measurement using two NIR instruments during the mirror-drawing task. A lack of interhemispheric integration was observed with schizophrenic patients. These observations suggest an application for NIRS in psychiatric disease management, as an addition to clinical monitoring at the bedside. A time resolved 64-channel optical imaging system was constructed. This consisted of three picosecond laser diodes and 64 channels of TAC and CFD systems. Image reconstruction for phantom model systems was performed. Time-resolved quantitative optical imaging will become real in the very near future.

Full Text

The Full Text of this article is available as a PDF (401.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Hazeki O., Tamura M. Quantitative analysis of hemoglobin oxygenation state of rat brain in situ by near-infrared spectrophotometry. J Appl Physiol (1985) 1988 Feb;64(2):796–802. doi: 10.1152/jappl.1988.64.2.796. [DOI] [PubMed] [Google Scholar]
  2. Hoshi Y., Mizukami S., Tamura M. Dynamic features of hemodynamic and metabolic changes in the human brain during all-night sleep as revealed by near-infrared spectroscopy. Brain Res. 1994 Aug 1;652(2):257–262. doi: 10.1016/0006-8993(94)90235-6. [DOI] [PubMed] [Google Scholar]
  3. Hoshi Y., Onoe H., Watanabe Y., Andersson J., Bergström M., Lilja A., Långström B., Tamura M. Non-synchronous behavior of neuronal activity, oxidative metabolism and blood supply during mental tasks in man. Neurosci Lett. 1994 May 19;172(1-2):129–133. doi: 10.1016/0304-3940(94)90679-3. [DOI] [PubMed] [Google Scholar]
  4. Hoshi Y., Tamura M. Detection of dynamic changes in cerebral oxygenation coupled to neuronal function during mental work in man. Neurosci Lett. 1993 Feb 5;150(1):5–8. doi: 10.1016/0304-3940(93)90094-2. [DOI] [PubMed] [Google Scholar]
  5. Kato T., Kamei A., Takashima S., Ozaki T. Human visual cortical function during photic stimulation monitoring by means of near-infrared spectroscopy. J Cereb Blood Flow Metab. 1993 May;13(3):516–520. doi: 10.1038/jcbfm.1993.66. [DOI] [PubMed] [Google Scholar]
  6. Maki A., Yamashita Y., Ito Y., Watanabe E., Mayanagi Y., Koizumi H. Spatial and temporal analysis of human motor activity using noninvasive NIR topography. Med Phys. 1995 Dec;22(12):1997–2005. doi: 10.1118/1.597496. [DOI] [PubMed] [Google Scholar]
  7. Okada F., Tokumitsu Y., Hoshi Y., Tamura M. Gender- and handedness-related differences of forebrain oxygenation and hemodynamics. Brain Res. 1993 Jan 22;601(1-2):337–342. doi: 10.1016/0006-8993(93)91733-9. [DOI] [PubMed] [Google Scholar]
  8. Okada F., Tokumitsu Y., Hoshi Y., Tamura M. Impaired interhemispheric integration in brain oxygenation and hemodynamics in schizophrenia. Eur Arch Psychiatry Clin Neurosci. 1994;244(1):17–25. doi: 10.1007/BF02279807. [DOI] [PubMed] [Google Scholar]
  9. Okada F., Tokumitsu Y., Takahashi N., Hoshi Y., Tamura M. Region-dependent asymmetrical or symmetrical variations in the oxygenation and hemodynamics of the brain due to different mental stimuli. Brain Res Cogn Brain Res. 1995 Jul;2(3):215–219. doi: 10.1016/0926-6410(95)90010-1. [DOI] [PubMed] [Google Scholar]
  10. Onoe H., Watanabe Y., Tamura M., Hayaishi O. REM sleep-associated hemoglobin oxygenation in the monkey forebrain studied using near-infrared spectrophotometry. Neurosci Lett. 1991 Aug 19;129(2):209–213. doi: 10.1016/0304-3940(91)90463-4. [DOI] [PubMed] [Google Scholar]
  11. Villringer A., Dirnagl U. Coupling of brain activity and cerebral blood flow: basis of functional neuroimaging. Cerebrovasc Brain Metab Rev. 1995 Fall;7(3):240–276. [PubMed] [Google Scholar]
  12. Villringer A., Planck J., Hock C., Schleinkofer L., Dirnagl U. Near infrared spectroscopy (NIRS): a new tool to study hemodynamic changes during activation of brain function in human adults. Neurosci Lett. 1993 May 14;154(1-2):101–104. doi: 10.1016/0304-3940(93)90181-j. [DOI] [PubMed] [Google Scholar]
  13. van der Zee P., Cope M., Arridge S. R., Essenpreis M., Potter L. A., Edwards A. D., Wyatt J. S., McCormick D. C., Roth S. C., Reynolds E. O. Experimentally measured optical pathlengths for the adult head, calf and forearm and the head of the newborn infant as a function of inter optode spacing. Adv Exp Med Biol. 1992;316:143–153. doi: 10.1007/978-1-4615-3404-4_17. [DOI] [PubMed] [Google Scholar]

Articles from Philosophical Transactions of the Royal Society B: Biological Sciences are provided here courtesy of The Royal Society

RESOURCES