Difference in the metabolic response to photic stimulation of the lateral geniculate nucleus and the primary visual cortex of infants: A fMRI study

Neuroscience Research

Volumn 38, Issue 1, 2000, Pages 63-70

  Morita, Tomoyo ^a   Kochiyama, Takanori ^a   Yamada, Hiroki ^b   Konishi, Yukuo ^b   Yonekura, Yoshiharu ^b   Matsumura, Michikazu ^a   Sadato, Norihiro ^c  

^a KYOTO UNIVERSITY   (Japan)

^b UNIVERSITY OF FUKUI   (Japan)

^c Psychophysiology Sect Natl I ^*  (Japan)

Author keywords

Brain activation; Functional magnetic resonance imaging (fMRI); Infant; Lateral geniculate nucleus; Primary visual cortex; Synaptogenesis

Indexed keywords

OXYGEN; PENTOBARBITAL;

ARTICLE; BRAIN DEVELOPMENT; BRAIN METABOLISM; EYELID; FEMALE; HUMAN; HUMAN EXPERIMENT; INFANT; LATERAL GENICULATE BODY; MALE; NERVE CELL STIMULATION; NORMAL HUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; OXYGEN CONSUMPTION; OXYGEN SUPPLY; PHOTOSTIMULATION; PRIORITY JOURNAL; SYNAPTOGENESIS; VISUAL CORTEX;

AGING; BLOOD FLOW VELOCITY; CEREBROVASCULAR CIRCULATION; FEMALE; GENICULATE BODIES; GESTATIONAL AGE; HUMAN; INFANT; MAGNETIC RESONANCE IMAGING; MALE; OXYGEN; PHOTIC STIMULATION; SUPPORT, NON-U.S. GOV'T; SYNAPSES; VISUAL CORTEX;

EID: 0034281989     PISSN: 01680102     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-0102(00)00146-2     Document Type: Article

References (42)

1. Altman D.I., Perlman J.M., Volpe J.J., Powers W.J. Cerebral oxygen metabolism in newborns. Pediatrics. 92:1993;99-104.
2. Barkovich A.J., Kjos B.O., Jackson D.E. Jr, Norman D. Normal maturation of the neonatal and infant brain: MR imaging at 1.5 T. Radiology. 166:1988;173-180.
3. Belliveau J., Kennedy D., McKinstry R., et al. Functional mapping of the human visual cortex by magnetic resonance imaging. Science. 254:1991;716-719.
4. Born P., Rostrup E., Leth H., Peitersen B., Lou H.C. Change of visually induced cortical activation patterns during development. Lancet. 347:1996;543.
5. Born P., Leth H., Miranda M.J., et al. Visual activation in infants and young children studied by functional magnetic resonance imaging. Pediatr. Res. 44:1998;578-583.
6. Bourgeois J.P., Rakic P. Changes of synaptic density in the primary visual cortex of the macaque monkey from fetal to adult stage. J. Neurosci. 13:1993;2801-2820.
7. Büchel C., Turner R., Friston K. Lateral geniculate activations can be detected using intersubject averaging and fMRI. Magn. Reson. Med. 38:1997;691-694.
8. Chen W., Kato T., Zhu X.H., Strupp J., Ogawa S., Ugurbil K. Mapping of lateral geniculate nucleus activation during visual stimulation in human brain using fMRI [published erratum appears in Magn. Reson. Med. 1998 Mar; 39(3):following 505]. Magn. Reson. Med. 39:1998;89-96.
9. Chi J.G., Dooling E.C., Gilles F.H. Gyral development of the human brain. Ann. Neurol. 1:1977;86-93.
10. 18F]FDG positron emission tomography. Science. 231:1986;840-843.
11. Fox P.T., Raichle M.E. Focal physiological uncoupling of cerebral blood flow and oxidative metabolism during somatosensory stimulation in human subjects. Proc. Natl. Acad. Sci. USA. 83:1986;1140-1144.
12. Friston K.J., Jezzard P., Turner R. Analysis of functional MRI time-series. Hum. Brain Mapp. 1:1994;153-171.
13. Friston K.J., Holmes A.P., Worsley K.J., Poline J.B., Frith C.D., Frackowiak R.S.J. Statistical parametric maps in functional imaging: a general linear approach. Hum. Brain Mapp. 2:1995a;189-210.
14. Friston K.J., Holmes A.P., Poline J.-B., et al. Analysis of fMRI time-series revisited. Neuroimage. 2:1995b;45-53.
15. Garey L.J., de Courten C. Structural development of the lateral geniculate nucleus and visual cortex in monkey and man. Behav. Brain Res. 10:1983;3-13.
16. Grinvald A., Frostig R.D., Siegel R.M., Bartfeld E. High-resolution optical imaging of functional brain architecture in the awake monkey. Proc. Natl. Acad. Sci. USA. 88:1991;11559-11563.
17. Herschkowitz N. Brain development in the fetus, neonate and infant. Biol. Neonate. 54:1988;1-19.
18. Hitchcock P.F., Hickey T.L. Prenatal development of the human lateral geniculate nucleus. J. Comp. Neurol. 194:1980;395-411.
19. Hobbs W.R., Rall T.W., Verdoorn T.A. Hypnotics and sedatives; ethanol. Hardman J.G., Goodman G., Gilman A., Limbird L.E. Goodman & Gilman's The Pharmacological Basis of Therapeutics. 1995;361-396 McGraw-Hill, New York.
20. Holstein G.R., Pasik T., Pasik P., Hamori J. Early postnatal development of the monkey visual system. II: elimination of retinogeniculate synapses. Brain Res. 352:1985;15-31.
21. Horton J.C., Landau K., Maeder P., Hoyt W.F. Magnetic resonance imaging of the human lateral geniculate body. Arch. Neurol. 47:1990;1201-1206.
22. Hu X., Le T.H., Ugurbil K. Evaluation of the early response in fMRI in individual subjects using short stimulus duration. Magn. Reson. Med. 37:1997;877-884.
23. Huttenlocher P.R., de Courten C., Garey L.J., Van der Loos H. Synaptogenesis in human visual cortex - evidence for synapse elimination during normal development. Neurosci. Lett. 33:1982;247-252.
24. Khan A.A., Wadhwa S., Bijlani V. Development of human lateral geniculate nucleus: an electron microscopic study. Int. J. Dev. Neurosci. 12:1994;661-672.
25. Kinnala A., Suhonen-Polvi H., Aarimaa T., et al. Cerebral metabolic rate for glucose during the first six months of life: an FDG positron emission tomography study. Arch. Dis. Child. Fetal Neonatal Ed. 74:1996;F153-F157.
26. Kwong K.K., Belliveau J.W., Chesler D.A., et al. Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation. Proc. Natl. Acad. Sci. USA. 89:1992;5675-5679.
27. Malonek D., Grinvald A. Interactions between electrical activity and cortical microcirculation revealed by imaging spectroscopy: implications for functional brain mapping. Science. 272:1996;551-554.
28. Martin E., Joeri P., Loenneker T., et al. Visual processing in infants and children studied using functional MRI. Pediatr. Res. 46:1999;135-140.
29. Menon R.S., Ogawa S., Hu X., Strupp J.P., Anderson P., Ugurbil K. BOLD based functional MRI at 4 Tesla includes a capillary bed contribution: echo-planar imaging correlates with previous optical imaging using intrinsic signals. Magn. Reson. Med. 33:1995;453-459.
30. Ogawa S., Lee T.M., Kay A.R., Tank D.W. Brain magnetic resonance imaging with contrast dependent on blood oxygenation. Proc. Natl. Acad. Sci. USA. 87:1990;9868-9872.
31. Ogawa S., Tank D.W., Menon R., et al. Intrinsic signal changes accompnying sensory stimulation: functional brain mapping with magnetic resonance imaging. Proc. Natl. Acad. Sci. USA. 89:1992;5951-5955.
32. Pauling L., Coryell C. The magnetic properties of and structure of hemoglobin, oxyhemoglobin and carbonmonoxyhemoglobin. Proc. Natl. Acad. Sci. USA. 22:1936;210-216.
33. Powers W.J., Rosenbaum J.L., Dence C.S., Markham J., Videen T.O. Cerebral glucose transport and metabolism in preterm human infants. J. Cereb. Blood Flow Metab. 18:1998;632-638.
34. Provis J.M., van Driel D., Billson F.A., Russell P. Human fetal optic nerve: overproduction and elimination of retinal axons during development. J. Comp. Neurol. 238:1985;92-100.
35. Raichle M.E. Circulatory and metabolic correlates of brain function in normal humans. Mountcastle V.M., Plum F., Geiger S.R. Handbook of Physiology. 1987;643-674 American Physiology Society, Bethesda, MD.
36. Rakic P. Prenatal genesis of connections subserving ocular dominance in the rhesus monkey. Nature. 261:1976;467-471.
37. Sadato N., Yonekura Y., Yamada H., Nakamura S., Waki A., Ishii Y. Activation patterns of covert word generation detected by functional MRI: comparison with 3D PET. J. Comput. Assist. Tomogr. 22:1998;945-952.
38. Takahashi T., Shirane R., Sato S., Yoshimoto T. Developmental changes of cerebral blood flow and oxygen metabolism in children. Am. J. Neuroradiol. 20:1999;917-922.
39. Wadhwa S., Takacs J., Bijlani V., Hamori J. Numerical estimates of GABA immunoreactive neurons in the human lateral geniculate nucleus in the prenatal period. Hum. Neurobiol. 6:1988;261-272.
40. Wolff J.R. Evidence for a dual role of GABA as a synaptic transmitter and a promoter of synaptogenesis. Adv. Biochem. Psychopharmacol. 29:1981;459-465.
41. Worsley K.J., Friston K.J. Analysis of fMRI time-series revisited - again. Neuroimage. 2:1995;173-181.
42. Yamada H., Sadato N., Konishi Y., et al. A rapid brain metabolic change in infants detected by fMRI. Neuroreport. 8:1997;3775-3778.