Evidence map›Paper›PMID 29161352›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2019

Delta Rhythm Orchestrates the Neural Activity Underlying the Resting State BOLD Signal via Phase-amplitude Coupling.

Saul Jaime, Hong Gu, Brian F Sadacca, Elliot A Stein, Jose E Cavazos, Yihong Yang, Hanbing Lu

Open access · hybridAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Frontiers in neural circuits · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Vascular and neural basis of the BOLD signal.Current opinion in neurobiology · 2019
    Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Intracranial Electrophysiology Reveals Reproducible Intrinsic Functional Connectivity within Human Brain Networks.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  18. Article
  19. 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

7 authors at 4 institutions in 1 country.

Saul JaimeNeuroimaging Research Branch, National Institute on Drug Abuse, National Institutes of Health, Baltimore, USA.
Hong GuNeuroimaging Research Branch, National Institute on Drug Abuse, National Institutes of Health, Baltimore, USA.
Brian F SadaccaCellular Neurobiology Research Branch, National Institute on Drug Abuse, National Institutes of Health, Baltimore, USA.
Elliot A SteinNeuroimaging Research Branch, National Institute on Drug Abuse, National Institutes of Health, Baltimore, USA.
Jose E CavazosGraduate School of Biomedical Sciences, UT Health-San Antonio, San Antonio, USA.
Yihong YangNeuroimaging Research Branch, National Institute on Drug Abuse, National Institutes of Health, Baltimore, USA.
Hanbing LuNeuroimaging Research Branch, National Institute on Drug Abuse, National Institutes of Health, Baltimore, USA.
National Institute on Drug Abuse · USNational Institutes of Health · USThe University of Texas Health Science Center at Houston · USThe University of Texas Health Science Center at San Antonio · US

Funding

Translational addiction neurobiologyZIADA000597 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI STEIN, ELLIOT A · 2013 to 2021
$6.2M
6 · The paper itself

Abstract

Spontaneous ongoing neuronal activity is a prominent feature of the mammalian brain. Temporal and spatial patterns of such ongoing activity have been exploited to examine large-scale brain network organization and function. However, the neurophysiological basis of this spontaneous brain activity as detected by resting-state functional Magnetic Resonance Imaging (fMRI) remains poorly understood. To this end, multi-site local field potentials (LFP) and blood oxygenation level-dependent (BOLD) fMRI were simultaneously recorded in the rat striatum along with local pharmacological manipulation of striatal activity. Results demonstrate that delta (δ) band LFP power negatively, while beta (β) and gamma (γ) band LFPs positively correlated with BOLD fluctuation. Furthermore, there was strong cross-frequency phase-amplitude coupling (PAC), with the phase of δ LFPs significantly modulating the amplitude of the high frequency signal. Enhancing dopaminergic neuronal activity significantly reduced ventral striatal functional connectivity, δ LFP-BOLD correlation, and the PAC effect. These data suggest that different frequency bands of the LFP contribute distinctively to BOLD spontaneous fluctuation and that PAC is the organizing mechanism through which low frequency LFPs orchestrate neural activity that underlies resting state functional connectivity.

Indexed as

AnimalsDelta RhythmMagnetic Resonance ImagingMaleNerve NetOxygen ConsumptionRatsRats, Sprague-DawleyRestVentral Striatum

Identifiers

PMID29161352
PMCPMC6490973
OpenAlexW2769433111

What OpenQuestion holds

Textmetadata
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.