Evidence map›Paper›PMID 38351131›Full record

ArticleeNeuro2024

The Paraventricular Thalamic Nucleus and Its Projections in Regulating Reward and Context Associations.

Dillon S McDevitt, Quinn W Wade, Greer E McKendrick, Jacob Nelsen, Mariya Starostina, Nam Tran, Julie A Blendy, Nicholas M Graziane

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eNeuro, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Brain network localization of anhedonia.Translational psychiatry · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Dillon S McDevittNeuroscience Program, Penn State College of Medicine, Hershey, Pennsylvania 17033.
Quinn W WadeDepartment of Anesthesiology and Perioperative Medicine, Penn State College of Medicine, Hershey, Pennsylvania 17033.
Greer E McKendrickNeuroscience Program, Penn State College of Medicine, Hershey, Pennsylvania 17033.
Jacob NelsenDoctor of Medicine Program, Penn State College of Medicine, Hershey, Pennsylvania 17033.
Mariya StarostinaDoctor of Medicine Program, Penn State College of Medicine, Hershey, Pennsylvania 17033.
Nam TranDoctor of Medicine Program, Penn State College of Medicine, Hershey, Pennsylvania 17033.ORCID https://orcid.org/0000-0002-8312-9197
Julie A BlendyDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.ORCID https://orcid.org/0000-0003-1705-9001
Nicholas M GrazianeDepartments of Anesthesiology and Perioperative Medicine and Pharmacology, Penn State College of Medicine, Hershey, Pennsylvania 17033 ngraziane@pennstatehealth.psu.edu.
Pennsylvania State University · USTranslational Therapeutics (United States) · US

Funding

Mapping opioid-dependence state transitions across structural, functional, and transcriptomic topologiesR01DA054374 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI BLENDY, JULIE A, CORDER, GREGORY · 2021 to 2025
$2.4M
NIDA NIH HHS R01 DA054374
6 · The paper itself

Abstract

The paraventricular thalamic nucleus (PVT) is a brain region that mediates aversive and reward-related behaviors as shown in animals exposed to fear conditioning, natural rewards, or drugs of abuse. However, it is unknown whether manipulations of the PVT, in the absence of external factors or stimuli (e.g., fear, natural rewards, or drugs of abuse), are sufficient to drive reward-related behaviors. Additionally, it is unknown whether drugs of abuse administered directly into the PVT are sufficient to drive reward-related behaviors. Here, using behavioral as well as pathway and cell-type specific approaches, we manipulate PVT activity as well as the PVT-to-nucleus accumbens shell (NAcSh) neurocircuit to explore reward phenotypes. First, we show that bath perfusion of morphine (10 µM) caused hyperpolarization of the resting membrane potential, increased rheobase, and decreased intrinsic membrane excitability in PVT neurons that project to the NAcSh. Additionally, we found that direct injections of morphine (50 ng) in the PVT of mice were sufficient to generate conditioned place preference (CPP) for the morphine-paired chamber. Mimicking the inhibitory effect of morphine, we employed a chemogenetic approach to inhibit PVT neurons that projected to the NAcSh and found that pairing the inhibition of these PVT neurons with a specific context evoked the acquisition of CPP. Lastly, using brain slice electrophysiology, we found that bath-perfused morphine (10 µM) significantly reduced PVT excitatory synaptic transmission on both dopamine D1 and D2 receptor-expressing medium spiny neurons in the NAcSh, but that inhibiting PVT afferents in the NAcSh was not sufficient to evoke CPP.

Indexed as

Midline Thalamic NucleiNeuronsAnimalsMiceMorphineNucleus AccumbensRewardMorphineconditioned place preferencemotivationnucleus accumbens shellopioidsparaventricular thalamic nucleusreward

Identifiers

PMID38351131
PMCPMC10883411
OpenAlexW4391773489

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.