Evidence map›Paper›PMID 38499210›Full record

ArticleBrain, behavior, and immunity2024

Knockdown of Tlr3 in dorsal striatum reduces ethanol consumption and acute functional tolerance in male mice.

Geoffrey A Dilly, Yuri A Blednov, Anna S Warden, Lubov Ezerskiy, Caleb Fleischer, Jesse D Plotkin, Shruti Patil, Elizabeth A Osterndorff-Kahanek, Jody Mayfield, R Dayne Mayfield and 2 more

Open access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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

12 authors at 2 institutions in 1 country.

Geoffrey A DillyWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States; Institute for Neuroscience, The University of Texas at Austin, Austin, TX 78712, United States; Department of Neuroscience, The University of Texas at Austin, Austin, TX 78712, United States; Department of Neurology, Dell Medical School, The University of Texas at Austin, Austin, TX 78712, United States.
Yuri A BlednovWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States.
Anna S WardenWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States.
Lubov EzerskiyWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States; Department of Neuroscience, The University of Texas at Austin, Austin, TX 78712, United States.
Caleb FleischerWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States; Department of Neuroscience, The University of Texas at Austin, Austin, TX 78712, United States.
Jesse D PlotkinWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States; Department of Neuroscience, The University of Texas at Austin, Austin, TX 78712, United States.
Shruti PatilWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States.
Elizabeth A Osterndorff-KahanekWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States.
Jody MayfieldWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States.
R Dayne MayfieldWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States; Department of Neuroscience, The University of Texas at Austin, Austin, TX 78712, United States.
Gregg E HomanicsDepartments of Anesthesiology & Perioperative Medicine, Neurobiology, and Pharmacology & Chemical Biology, University of Pittsburgh, Pittsburgh, PA 15261, United States.
Robert O MessingWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX 78712, United States; Institute for Neuroscience, The University of Texas at Austin, Austin, TX 78712, United States; Department of Neuroscience, The University of Texas at Austin, Austin, TX 78712, United States; Department of Neurology, Dell Medical School, The University of Texas at Austin, Austin, TX 78712, United States. Electronic address: romessing@austin.utexas.edu.
The University of Texas at Austin · USUniversity of Pittsburgh · US

Funding

GENE EXPRESSION IN THE HUMAN ALCOHOLIC BRAINR01AA012404 · NIAAA · UNIVERSITY OF TEXAS AUSTIN · PI MAYFIELD, ROY DAYNE · 2000 to 2025
$10.7M
INIA: ANIMAL COREU01AA013520 · NIAAA · UNIVERSITY OF TEXAS AUSTIN · PI YURI A BLEDNOV, ROBERT O. MESSING · 2001 to 2026
$9.5M
Neurochemical & Behavioral Correlates of ETOH EffectsT32AA007471 · NIAAA · UNIVERSITY OF TEXAS AUSTIN · PI Kimberly Nixon · 1987 to 2026
$9.2M
Role of noncoding RNA in alcohol actionU01AA020889 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Sean P Farris, Gregg E. Homanics · 2011 to 2026
$7.1M
Next Generation Sequencing of Human Alcoholic BrainU01AA020926 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI Roy DAYNE MAYFIELD · 2011 to 2026
$6.7M
Integrative Neuroscience Initiative on AlcoholismU24AA025479 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI ROBERT O. MESSING · 2017 to 2026
$5.0M
Cell-type specific central amygdala neurotransmission in alcohol dependenceF31AA029635 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI DILLY, GEOFFREY A · 2021 to 2022
$74k
NIAAA NIH HHS F31 AA029635NIAAA NIH HHS R01 AA012404NIAAA NIH HHS T32 AA007471NIAAA NIH HHS U01 AA013520NIAAA NIH HHS U01 AA020889NIAAA NIH HHS U01 AA020926NIAAA NIH HHS U24 AA025479
6 · The paper itself

Abstract

Systemic activation of toll-like receptor 3 (TLR3) signaling using poly(I:C), a TLR3 agonist, drives ethanol consumption in several rodent models, while global knockout of Tlr3 reduces drinking in C57BL/6J male mice. To determine if brain TLR3 pathways are involved in drinking behavior, we used CRISPR/Cas9 genome editing to generate a Tlr3 floxed (Tlr3

Indexed as

EthanolToll-Like Receptor 3Alcohol DrinkingAnimalsMaleMiceMice, Inbred C57BLPoly I-CSignal TransductionEthanolPoly I-CToll-Like Receptor 3Acute functional tolerance to ethanolDiazepamPoly(I:C)Rotarod ataxiaTlr3(F/F) miceTlr3 knockdown in dorsal striatumTwo-bottle choice every-other-day ethanol consumption

Identifiers

PMID38499210
PMCPMC11007683
OpenAlexW4392877904

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.