Evidence map›Paper›PMID 20371821›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Early suppressive mechanisms and the negative blood oxygenation level-dependent response in human visual cortex.

Alex R Wade, Jess Rowland

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.1field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 50 citations in OpenAlex.

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  4. BOLD response delays represent local cortical processing.Cerebral cortex (New York, N.Y. : 1991) · 2026
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  11. Dynamic metabolic changes in human visual cortex in regions with positive and negative blood oxygenation level-dependent response.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2019
    Article
  12. Asymmetries between achromatic and chromatic extraction of 3D motion signals.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  13. Article
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  15. Article
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  17. Normalization in human somatosensory cortex.Journal of neurophysiology · 2015
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  18. Article
  19. Article
  20. On the role of suppression in spatial attention: evidence from negative BOLD in human subcortical and cortical structures.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Alex R WadeSmith-Kettlewell Eye Research Institute, San Francisco, California 94115, USA. wade@wadelab.net
Jess Rowland
Smith-Kettlewell Eye Research Institute · USSmith-Kettlewell Eye Research Institute · US

Funding

A Multimodal Study of Human Chromatic PathwaysR01EY018157 · NEI · SMITH-KETTLEWELL EYE RESEARCH INSTITUTE · PI WADE, ALEXANDER R. · 2008 to 2010
$1.5M
GENETIC DETERMINANTS OF MULTISTEP ORAL TUMORIGENESISR01DE013157 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HITTELMAN, WALTER N. · 1999 to 2006
$1.4M
The Organization of Suppression in Human Visual CortexR01EY017071 · NEI · SMITH-KETTLEWELL EYE RESEARCH INSTITUTE · PI MCKEE, SUZANNE P · 2006 to 2008
$749k
NEI NIH HHS R01 EY013157NEI NIH HHS R01 EY017071NEI NIH HHS R01 EY018157NIDCR NIH HHS R01 DE013157
6 · The paper itself

Abstract

Functional magnetic resonance imaging (fMRI) studies of early sensory cortex often measure stimulus-driven increases in the blood oxygenation level-dependent (BOLD) signal. However, these positive responses are frequently accompanied by reductions in the BOLD signal in adjacent regions of cortex. Although this negative BOLD response (NBR) is thought to result from neuronal suppression, the precise relationship between local activity, suppression, and perception remains unknown. By measuring BOLD signals in human primary visual cortex while varying the baseline contrast levels in the region affected by the NBR, we tested three physiologically plausible computational models of neuronal modulation that could explain this phenomenon: a subtractive model, a response gain model, and a contrast gain model. We also measured the ability of isoluminant contrast to generate an NBR. We show that the NBR can be modeled as a pathway-specific contrast gain modulation that is strongest outside the fovea. We found a similar spatial bias in a psychophysical study using identical stimuli, although these data indicated a response gain rather than a contrast gain mechanism. We reconcile these findings by proposing (1) that the NBR is associated with a long-range suppressive mechanism that hyperpolarizes a subset of magnocellularly driven neurons at the input to V1, (2) that this suppression is broadly tuned to match the spatial features of the mask region, and (3) that increasing the baseline contrast in the suppressed region drives all neurons in the input layer, reducing the relative contribution of the suppressing subpopulation in the fMRI signal.

Indexed as

Magnetic Resonance ImagingPhotic StimulationAdultAgedFemaleHumansMaleMiddle AgedNeural InhibitionOxygenSignal TransductionTime FactorsVisual CortexYoung AdultOxygen

Identifiers

PMID20371821
PMCPMC3523120
OpenAlexW2027063232

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.