Skip to main content

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Blog
    • Collections
    • Podcast
  • TOPICS
    • Cognition and Behavior
    • Development
    • Disorders of the Nervous System
    • History, Teaching and Public Awareness
    • Integrative Systems
    • Neuronal Excitability
    • Novel Tools and Methods
    • Sensory and Motor Systems
  • ALERTS
  • FOR AUTHORS
  • ABOUT
    • Overview
    • Editorial Board
    • For the Media
    • Privacy Policy
    • Contact Us
    • Feedback
  • SUBMIT

User menu

Search

  • Advanced search
eNeuro
eNeuro

Advanced Search

 

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Blog
    • Collections
    • Podcast
  • TOPICS
    • Cognition and Behavior
    • Development
    • Disorders of the Nervous System
    • History, Teaching and Public Awareness
    • Integrative Systems
    • Neuronal Excitability
    • Novel Tools and Methods
    • Sensory and Motor Systems
  • ALERTS
  • FOR AUTHORS
  • ABOUT
    • Overview
    • Editorial Board
    • For the Media
    • Privacy Policy
    • Contact Us
    • Feedback
  • SUBMIT
PreviousNext
Research ArticleNew Research, Cognition and Behavior

Theta Oscillations Organize Spiking Activity in Higher-Order Visual Thalamus during Sustained Attention

Chunxiu Yu, Yuhui Li, Iain M. Stitt, Zhe Charles Zhou, Kristin K. Sellers and Flavio Frohlich
eNeuro 28 February 2018, 5 (1) ENEURO.0384-17.2018; https://doi.org/10.1523/ENEURO.0384-17.2018
Chunxiu Yu
1Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Chunxiu Yu
Yuhui Li
1Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Iain M. Stitt
1Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Zhe Charles Zhou
1Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
5Neuroscience Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kristin K. Sellers
1Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Kristin K. Sellers
Flavio Frohlich
1Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
2Department of Neurology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
3Department of Biomedical Engineering, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
4Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
5Neuroscience Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Flavio Frohlich
  • Article
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF
Loading

Article Figures & Data

Figures

  • Figure 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 1.

    Sustained attention task in freely-moving ferrets. A, Illustration of trial sequences of the 5-CSRTT. Each trial begins with illumination of the water spout, which is centrally placed on the back wall of the chamber. The ferret initiates the trial by approaching the water spout, which is equipped with an IR proximity sensor. Then, the spout light is extinguished and the 5-s delay period starts during which the animal is required to sustain attention to the five windows on the front wall of the chamber. A white solid square (stimulus) will randomly present in one of five windows after the delay ends. Nose-poke to the stimulus window during stimulus presentation (2 s) or in the first 2 s after stimulus offset (HP) triggers a tone and delivery of water reward at the spout (correct trial, left). Touch by the ferret is indicated with an asterisk. If the ferret responds before the stimulus (PreTouch), or touches an incorrect window (MissTouch), or fails to respond before the end of the HP (omission), a 6-s time-out (TO) period is introduced where the house light is on and no water is delivered (right). After collecting the reward (8-s time window) or at the end of the TO period, a new trial can be started. B, Representative photographs of one animal during a single trial: a, initiation; b, turn to the stimulus windows (numbered 1 through 5 in subpanel a); c–d, paws on the platform and checking for occurrence of stimulus; e, stimulus on; f, find the stimulus; g, nose poke the stimulus window; h, turn back to collect the reward; i, collect the reward; j, complete trajectory for a single trial obtained from video tracking; k, heatmap of animal locations during the session. Time stamps are shown in the corner of each frame. C, Behavioral performance. Mean accuracy and omission rates across sessions. Error bars: SEM across sessions. D, Mean distance between animal location and stimulus location as a function of time for correct trials. The shorter distances to middle windows (W2 – W4) indicate that animals were centered relative to the stimulus windows before stimulus onset. E, Distribution of touch reaction times (RT) for correct trials. In most trials, the correct window was touched during stimulus presentation (RT < 2 s).

  • Figure 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 2.

    Single-unit responses during task performance. A, Representative coronal section; stars indicate the estimated locations of the electrode tips. Electrodes outside of LP/pulvinar (LP/Pulv) were excluded. LGN, lateral geniculate nucleus; MGN, medial geniculate nucleus; PO, nucleus of the posterior group; SGN, suprageniculate nucleus. B, top, Example of high-pass filtered raw trace from representative recording session. Bottom, Action potentials of two representative single units. C, Peri-event raster plots (top) and peri-event histograms of the corresponding firing rates (bottom) of two representative neurons. The unit on the left exhibited an increasing firing during the delay period, whereas the unit on the right did not show such modulation but rather increased its firing rate after stimulus onset. D, Z-score normalized population firing rate of attention-modulated (red, n = 130) and non-attention-modulated units (black, n = 129) in correct trials (solid lines) and in incorrect trials (dotted lines). Attention-modulated units gradually increased their firing rate during the delay period. Both neuron types displayed a transient increase in firing rate after stimulus onset, with stronger responses in attention-modulated neurons. Shaded areas indicate SEM. E, Peri-event raster plots from all the attention-modulated (red, n = 130) and non-attention-modulated units (black, n = 129) in all correct trials. Units from each category are sorted by their mean firing rate in the delay period.

  • Figure 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 3.

    Interaction of spiking activity and the LFP in the θ band. A–D, SFC across sessions and animals for different task epochs for attention-modulated (red) and non-attention modulated units (black). A, Before initiation. B, Delay period (from initiation to stimulus onset). C, Before touch (from stimulus onset to touch response). D, After touch. The inset in B shows the STA of the LFP averaged across the attention-modulated (red) and non-attention-modulated units (black), and the shuffle control (green) in the 5-s delay period for all correct trials. The vertical dashed line indicates the spike time. Shaded areas both in the SFC plots and in the STA plot represent SEM. E, SFC of attention-modulated and non-attention-modulated units in θ band (4–6 Hz) for different task epochs. θ Coherence was differentially modulated by task performance. Attention-modulated units showed significantly higher coherence than non-attention-modulated units at all task epochs, except after touch. For attention-modulated units, θ coherence increased during the delay period compared to before trial initiation and reached the maximum before touch. No change in coherence occurred for non-attention-modulated units during the task; *p < 0.05; NS indicates p > 0.05. Error bars represent SEM.

  • Figure 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 4.

    Task-modulated θ/γ PAC. A, Modulation of θ power during task performance. θ Power gradually increased and was maintained during the delay period and peaked between stimulus onset and screen touch. Shaded area represents SEM. An example LFP trace (bandpass in 1–20 Hz) is displayed on the top and shows the θ oscillation throughout a trial. B, Heatmap of PAC during task performance shows selective coupling of θ and γ oscillations. An example LFP trace (bandpass in 1–100 Hz) is superimposed on the heatmap and shows γ-θ oscillation nesting. C, Task-dependent modulation of time-resolved θ/γ PAC. θ/γ PAC was elevated throughout the delay period and decreased after screen touch. Shaded area shows SEM. D, Modulation of γ power during task performance. γ Power gradually decreased during the delay period. Shaded area represents SEM.

Back to top

In this issue

eneuro: 5 (1)
eNeuro
Vol. 5, Issue 1
January/February 2018
  • Table of Contents
  • Index by author
Email

Thank you for sharing this eNeuro article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Theta Oscillations Organize Spiking Activity in Higher-Order Visual Thalamus during Sustained Attention
(Your Name) has forwarded a page to you from eNeuro
(Your Name) thought you would be interested in this article in eNeuro.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
View Full Page PDF
Citation Tools
Theta Oscillations Organize Spiking Activity in Higher-Order Visual Thalamus during Sustained Attention
Chunxiu Yu, Yuhui Li, Iain M. Stitt, Zhe Charles Zhou, Kristin K. Sellers, Flavio Frohlich
eNeuro 28 February 2018, 5 (1) ENEURO.0384-17.2018; DOI: 10.1523/ENEURO.0384-17.2018

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article
Share
Theta Oscillations Organize Spiking Activity in Higher-Order Visual Thalamus during Sustained Attention
Chunxiu Yu, Yuhui Li, Iain M. Stitt, Zhe Charles Zhou, Kristin K. Sellers, Flavio Frohlich
eNeuro 28 February 2018, 5 (1) ENEURO.0384-17.2018; DOI: 10.1523/ENEURO.0384-17.2018
Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Significance Statement
    • Introduction
    • Materials and Methods
    • Results
    • Discussion
    • Footnotes
    • References
    • Synthesis
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF

Keywords

  • 5-CSRTT
  • ferret
  • oscillations
  • sustained attention
  • thalamus
  • θ-γ coupling

Responses to this article

Respond to this article

Jump to comment:

No eLetters have been published for this article.

Related Articles

Cited By...

More in this TOC Section

New Research

  • A Very Fast Time Scale of Human Motor Adaptation: Within Movement Adjustments of Internal Representations during Reaching
  • Optogenetic Activation of β-Endorphin Terminals in the Medial Preoptic Nucleus Regulates Female Sexual Receptivity
  • Hsc70 Ameliorates the Vesicle Recycling Defects Caused by Excess α-Synuclein at Synapses
Show more New Research

Cognition and Behavior

  • Visual Speech Reduces Cognitive Effort as Measured by EEG Theta Power and Pupil Dilation
  • A progressive ratio task with costly resets reveals adaptive effort-delay tradeoffs
  • Luminance Matching in Cognitive Pupillometry Is Not Enough: The Curious Case of Orientation
Show more Cognition and Behavior

Subjects

  • Cognition and Behavior
  • Home
  • Alerts
  • Follow SFN on BlueSky
  • Visit Society for Neuroscience on Facebook
  • Follow Society for Neuroscience on Twitter
  • Follow Society for Neuroscience on LinkedIn
  • Visit Society for Neuroscience on Youtube
  • Follow our RSS feeds

Content

  • Early Release
  • Current Issue
  • Latest Articles
  • Issue Archive
  • Blog
  • Browse by Topic

Information

  • For Authors
  • For the Media

About

  • About the Journal
  • Editorial Board
  • Privacy Notice
  • Contact
  • Feedback
(eNeuro logo)
(SfN logo)

Copyright © 2025 by the Society for Neuroscience.
eNeuro eISSN: 2373-2822

The ideas and opinions expressed in eNeuro do not necessarily reflect those of SfN or the eNeuro Editorial Board. Publication of an advertisement or other product mention in eNeuro should not be construed as an endorsement of the manufacturer’s claims. SfN does not assume any responsibility for any injury and/or damage to persons or property arising from or related to any use of any material contained in eNeuro.