Literature DB >> 9345542

Frequency variation of a pattern-flash visual stimulus during PET differentially activates brain from striate through frontal cortex.

M J Mentis1, G E Alexander, C L Grady, B Horwitz, J Krasuski, P Pietrini, T Strassburger, H Hampel, M B Schapiro, S I Rapoport.   

Abstract

We evaluate regional cerebral blood flow (rCBF) in 19 healthy elderly subjects, mean age 64 +/- 11 (SD, years), during a passive visual stimulus in which pattern-flash frequency was parametrically manipulated. Using goggles with a grid of red lights imbedded into each lens, we performed five positron emission tomography (PET) H2(15)O water scans on each subject at alternating (left to right eye) flash frequencies of 0, 1, 4, 7, and 14 Hz. We found a biphasic rising and falling rCBF response in the striate cortex (7 Hz peak) and left anterior cingulate (4 Hz peak), 1 Hz activation in left middle temporal gyrus (V5), monotonically increasing rCBF in posterior areas (lateral and inferior visual association areas, Brodmann 18 and 19), and monotonically decreasing rCBF in anterior areas (frontal, cingulate, and superior temporal) predominantly in right hemisphere. We suggest the striate rCBF changes at all frequencies primarily reflect lateral geniculate input, the middle temporal activation at 1 Hz reflects perception of apparent motion, and the posterior extrastriate rCBF monotonic increase represents a neural response to increasing luminance intensity and form and color complexity that occur as pattern-flash frequency increases. The anterior monotonic rCBF decrease may represent active cross-modal functional suppression of brain areas irrelevant for processing the passive visual stimulus. Pattern-flash rCBF responses were highly reproducible (no series effect), more so in posterior than in anterior brain regions. The reproducibility and systematically changing rCBF responses to this passive stimulus suggest that it could be successfully used as a disease probe to evaluate neural function and drug effects in cognitively impaired patients.

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Year:  1997        PMID: 9345542     DOI: 10.1006/nimg.1997.0256

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  19 in total

1.  Detection and quantification of a wide range of fMRI temporal responses using a physiologically-motivated basis set.

Authors:  Michael P Harms; Jennifer R Melcher
Journal:  Hum Brain Mapp       Date:  2003-11       Impact factor: 5.038

2.  Determination of individual stimulus--response curves in the visual cortex.

Authors:  Rogier E Hagenbeek; Serge A R B Rombouts; Bob W van Dijk; Frederik Barkhof
Journal:  Hum Brain Mapp       Date:  2002-12       Impact factor: 5.038

3.  BOLD fMRI and DTI in strabismic amblyopes following occlusion therapy.

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4.  fMRI responses in medial frontal cortex that depend on the temporal frequency of visual input.

Authors:  Ramesh Srinivasan; Eleonora Fornari; Maria G Knyazeva; Reto Meuli; Philippe Maeder
Journal:  Exp Brain Res       Date:  2007-02-13       Impact factor: 1.972

5.  Long-lasting connectivity changes induced by intensive first-person shooter gaming.

Authors:  Davide Momi; Carmelo L Smeralda; Giorgio Di Lorenzo; Francesco Neri; Simone Rossi; Alessandro Rossi; Emiliano Santarnecchi
Journal:  Brain Imaging Behav       Date:  2021-06       Impact factor: 3.978

6.  Imaging signal transduction via arachidonic acid in the human brain during visual stimulation, by means of positron emission tomography.

Authors:  Giuseppe Esposito; Giampiero Giovacchini; Margaret Der; Jeih-San Liow; Abesh K Bhattacharjee; Kaizong Ma; Peter Herscovitch; Michael Channing; William C Eckelman; Mark Hallett; Richard E Carson; Stanley I Rapoport
Journal:  Neuroimage       Date:  2006-12-29       Impact factor: 6.556

7.  Modeling the effective connectivity of the visual network in healthy and photosensitive, epileptic baboons.

Authors:  C Ákos Szabó; Felipe S Salinas; Karl Li; Crystal Franklin; M Michelle Leland; Peter T Fox; Angela R Laird; Shalini Narayana
Journal:  Brain Struct Funct       Date:  2015-03-07       Impact factor: 3.270

8.  Influence of contrast-reversing frequency on the amplitude and spatial distribution of visual cortex hemodynamic responses.

Authors:  Karolina Bejm; Stanisław Wojtkiewicz; Piotr Sawosz; Maciej Perdziak; Zanna Pastuszak; Aleh Sudakou; Petro Guchek; Adam Liebert
Journal:  Biomed Opt Express       Date:  2019-11-15       Impact factor: 3.732

9.  Human cerebral activation during steady-state visual-evoked responses.

Authors:  Maria A Pastor; Julio Artieda; Javier Arbizu; Miguel Valencia; Jose C Masdeu
Journal:  J Neurosci       Date:  2003-12-17       Impact factor: 6.167

10.  Nonlinear changes in brain activity during continuous word repetition: an event-related multiparametric functional MR imaging study.

Authors:  R E Hagenbeek; S A R B Rombouts; D J Veltman; J W Van Strien; M P Witter; P Scheltens; F Barkhof
Journal:  AJNR Am J Neuroradiol       Date:  2007-09-20       Impact factor: 3.825

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