Evidence map›Paper›PMID 31301327›Full record

ReviewNeurochemistry international2019

Dopaminergic cellular and circuit contributions to kappa opioid receptor mediated aversion.

Elyssa B Margolis, Anushree N Karkhanis

Open access · greenAbstract readReview
In one paragraph

Review in Neurochemistry international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

34 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
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  4. Kappa Opioid Receptors Control a Stress-Sensitive Brain Circuit and Drive Cocaine Seeking.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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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

2 authors at 2 institutions in 1 country.

Elyssa B MargolisDepartment of Neurology, Alcohol and Addiction Research Group, University of California, San Francisco, 675 Nelson Rising Lane, Box 0444, San Francisco, CA, 94143, USA. Electronic address: elyssa.margolis@ucsf.edu.
Anushree N KarkhanisDepartment of Psychology, Developmental Exposure Alcohol Research Center, Center for Developmental and Behavioral Neuroscience, Binghamton University - SUNY, 4400 Vestal Parkway East, Binghamton, NY, 13902, USA. Electronic address: akarkhan@binghamton.edu.
Alcohol Research Group · USBinghamton University · US

Funding

Heterogeneity of Ventral Tegmental Area Neurons and Opioid RewardR01DA030529 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARGOLIS, ELYSSA · 2011 to 2015
$1.8M
The role of the VTA-lateral habenula circuit in opioid mediated behaviorsR01DA042025 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARGOLIS, ELYSSA · 2017 to 2021
$1.8M
Impact of early life stress on accumbal kappa opioid signaling and ethanol intakeK01AA023874 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KARKHANIS, ANUSHREE N · 2016 to 2020
$673k
NIAAA NIH HHS K01 AA023874NIDA NIH HHS R01 DA030529NIDA NIH HHS R01 DA042025
6 · The paper itself

Abstract

Neural circuits that enable an organism to protect itself by promoting escape from immediate threat and avoidance of future injury are conceptualized to carry an "aversive" signal. One of the key molecular elements of these circuits is the kappa opioid receptor (KOR) and its endogenous peptide agonist, dynorphin. In many cases, the aversive response to an experimental manipulation can be eliminated by selective blockade of KOR function, indicating its necessity in transmitting this signal. The dopamine system, through its contributions to reinforcement learning, is also involved in processing of aversive stimuli, and KOR control of dopamine in the context of aversive behavioral states has been intensely studied. In this review, we have discussed the multiple ways in which the KORs regulate dopamine dynamics with a central focus on dopamine neurons and projections from the ventral tegmental area. At the neuronal level, KOR agonists inhibit dopamine neurons both in the somatodendritic region as well as at terminal release sites, through various signaling pathways and ion channels, and these effects are specific to different synaptic sites. While the dominant hypotheses are that aversive states are driven by decreases in dopamine and increases in dynorphin, reported exceptions to these patterns indicate these ideas require refinement. This is critical given that KOR is being considered as a target for development of new therapeutics for anxiety, depression, pain, and other psychiatric disorders.

Indexed as

AmygdalaAnimalsAvoidance LearningDopamineDopaminergic NeuronsDynorphinsForecastingLearningNucleus AccumbensPunishmentReceptors, Opioid, kappaReinforcement, PsychologySignal TransductionVentral Tegmental AreaDopamineDynorphinsReceptors, Opioid, kappa

Identifiers

PMID31301327
PMCPMC6702044
OpenAlexW2946072318

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.