Evidence map›Paper›PMID 29305936›Full record

ReviewProgress in neuro-psychopharmacology & biological psychiatry2018

Modeling cocaine relapse in rodents: Behavioral considerations and circuit mechanisms.

Mitchell R Farrell, Hannah Schoch, Stephen V Mahler

Abstract readReview
In one paragraph

Review in Progress in neuro-psychopharmacology & biological psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
–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

49 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  9. Article
  10. A large-scale c-Fos brain mapping study on extinction of cocaine-primed reinstatement.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  11. Astrocyte CaFrontiers in cellular neuroscience · 2024
    Article
  12. Article
  13. Dopamine D3 Receptor Modulates Akt/mTOR and ERKInternational journal of molecular sciences · 2023
    Article
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  16. Review
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  18. Review
  19. PPL-103: A mixed opioid partial agonist with desirable anti-cocaine properties.Progress in neuro-psychopharmacology & biological psychiatry · 2022
    Article
  20. 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

3 authors.

Mitchell R FarrellDepartment of Neurobiology & Behavior, University of California, 1203 McGaugh Hall, Irvine, United States.
Hannah SchochDepartment of Neurobiology & Behavior, University of California, 1203 McGaugh Hall, Irvine, United States.
Stephen V MahlerDepartment of Neurobiology & Behavior, University of California, 1203 McGaugh Hall, Irvine, United States. Electronic address: mahlers@uci.edu.

Funding

Role of Ventral Pallidum Projection to VTA in Reinstatement of Cocaine SeekingR00DA035251 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI MAHLER, STEPHEN VINCENT · 2015 to 2017
$756k
NIDA NIH HHS R00 DA035251
6 · The paper itself

Abstract

Addiction is a chronic relapsing disorder, in that most addicted individuals who choose to quit taking drugs fail to maintain abstinence in the long-term. Relapse is especially likely when recovering addicts encounter risk factors like small "priming" doses of drug, stress, or drug-associated cues and locations. In rodents, these same factors reinstate cocaine seeking after a period of abstinence, and extensive preclinical work has used priming, stress, or cue reinstatement models to uncover brain circuits underlying cocaine reinstatement. Here, we review common rat models of cocaine relapse, and discuss how specific features of each model influence the neural circuits recruited during reinstated drug seeking. To illustrate this point, we highlight the surprisingly specific roles played by ventral pallidum subcircuits in cocaine seeking reinstated by either cocaine-associated cues, or cocaine itself. One goal of such studies is to identify, and eventually to reverse the specific circuit activity that underlies the inability of some humans to control their drug use. Based on preclinical findings, we posit that circuit activity in humans also differs based on the triggers that precipitate craving and relapse, and that associated neural responses could help predict the triggers most likely to elicit relapse in a given person. If so, examining circuit activity could facilitate diagnosis of subgroups of addicted people, allowing individualized treatment based on the most problematic risk factors.

Indexed as

Cocaine-Related DisordersAnimalsBrainCocaineDisease Models, AnimalDrug-Seeking BehaviorExtinction, PsychologicalHumansNeural PathwaysRecurrenceRodentiaSelf AdministrationCocaineNeural circuitsReinstatementSelf-administrationVentral pallidumVoluntary abstinence

Identifiers

PMID29305936
PMCPMC6034989

What OpenQuestion holds

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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.