Evidence map›Paper›PMID 38485258›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2024

Visual Corticotectal Neurons in Awake Rabbits: Receptive Fields and Driving Monosynaptic Thalamocortical Inputs.

Chuyi Su, Rosangela F Mendes-Platt, Jose-Manuel Alonso, Harvey A Swadlow, Yulia Bereshpolova

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. A Neural Model for V1 That Incorporates Dendritic Nonlinearities and Backpropagating Action Potentials.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  2. Fast-Spike Interneurons in Visual Cortical Layer 5: Heterogeneous Response Properties Are Related to Thalamocortical Connectivity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  3. 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

5 authors.

Chuyi SuDepartment of Psychological Sciences, University of Connecticut, Storrs, Connecticut.
Rosangela F Mendes-PlattDepartment of Psychological Sciences, University of Connecticut, Storrs, Connecticut.
Jose-Manuel AlonsoDepartment of Psychological Sciences, University of Connecticut, Storrs, Connecticut.ORCID 0000-0002-8066-8080
Harvey A SwadlowDepartment of Psychological Sciences, University of Connecticut, Storrs, Connecticut harvey.swadlow@uconn.edu.ORCID 0000-0003-1477-3250
Yulia BereshpolovaDepartment of Psychological Sciences, University of Connecticut, Storrs, Connecticut.ORCID 0000-0002-7117-7255

Funding

Thalamortical processing of visual information during alert and non-alert brain statesR01EY028905 · NEI · UNIVERSITY OF CONNECTICUT STORRS · PI SWADLOW, HARVEY A · 2018 to 2021
$1.6M
Cellular Mechanisms of State-Dependent Processing in Visual CortexR01EY034503 · NEI · UNIVERSITY OF CONNECTICUT STORRS · PI Yulia Bereshpolova · 2023 to 2026
$1.6M
Thalamocortical Architecture of a Visual Cortex Without Orientation ColumnsR01EY024946 · NEI · UNIVERSITY OF CONNECTICUT STORRS · PI SWADLOW, HARVEY A · 2015 to 2017
$1.2M
NEI NIH HHS R01 EY024946NEI NIH HHS R01 EY028905NEI NIH HHS R01 EY034503
6 · The paper itself

Abstract

The superior colliculus receives powerful synaptic inputs from corticotectal neurons in the visual cortex. The function of these corticotectal neurons remains largely unknown due to a limited understanding of their response properties and connectivity. Here, we use antidromic methods to identify corticotectal neurons in awake male and female rabbits, and measure their axonal conduction times, thalamic inputs and receptive field properties. All corticotectal neurons responded to sinusoidal drifting gratings with a nonlinear (nonsinusoidal) increase in mean firing rate but showed pronounced differences in their ON-OFF receptive field structures that we classified into three groups, Cx, S2, and S1. Cx receptive fields had highly overlapping ON and OFF subfields as classical complex cells, S2 had largely separated ON and OFF subfields as classical simple cells, and S1 had a single ON or OFF subfield. Thus, all corticotectal neurons are homogeneous in their nonlinear spatial summation but very heterogeneous in their spatial integration of ON and OFF inputs. The Cx type had the fastest conducting axons, the highest spontaneous activity, and the strongest and fastest visual responses. The S2 type had the highest orientation selectivity, and the S1 type had the slowest conducting axons. Moreover, our cross-correlation analyses found that a subpopulation of corticotectal neurons with very fast conducting axons and high spontaneous firing rates (largely "Cx" type) receives monosynaptic input from retinotopically aligned thalamic neurons. This previously unrecognized fast-conducting thalamic-mediated corticotectal pathway may provide specialized information to superior colliculus and prime recipient neurons for subsequent corticotectal or retinal synaptic input.

Indexed as

NeuronsSynapsesThalamusVisual CortexVisual PathwaysWakefulnessAction PotentialsAnimalsFemaleMalePhotic StimulationRabbitsSuperior ColliculiVisual Fieldsantidromicawake statecorticotectallayer 5thalamocorticalthalamo-corticotectal

Identifiers

PMID38485258
PMCPMC11079980

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.