Evidence map›Paper›PMID 28412411›Full record

ArticleProgress in neuro-psychopharmacology & biological psychiatry2017

Mirtazapine and ketanserin alter preference for gambling-like schedules of reinforcement in rats.

Amanda L Persons, Stephanie E Tedford, T Celeste

Abstract read
In one paragraph

Article in Progress in neuro-psychopharmacology & biological psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 52% 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, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Methylation Patterns of theFrontiers in psychiatry · 2020
    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 at 1 institution in 1 country.

Amanda L PersonsDepartment of Pharmacology, Rush University Medical Center, Chicago, IL, United States; Department of Physician Assistant Studies, Rush University Medical Center, Chicago, IL, United States; Center for Compulsive Behavior and Addiction, Rush University Medical Center, Chicago, IL, United States. Electronic address: Amanda_L_Persons@rush.edu.
Stephanie E TedfordDepartment of Pharmacology, Rush University Medical Center, Chicago, IL, United States; Center for Compulsive Behavior and Addiction, Rush University Medical Center, Chicago, IL, United States.
T CelesteDepartment of Pharmacology, Rush University Medical Center, Chicago, IL, United States; Department of Psychiatry, Rush University Medical Center, Chicago, IL, United States; Center for Compulsive Behavior and Addiction, Rush University Medical Center, Chicago, IL, United States.
Rush University Medical Center · US

Funding

A novel rodent model of dopamine agonist-induced impulsive control disordersR21NS074014 · NINDS · RUSH UNIVERSITY MEDICAL CENTER · PI NAPIER, T. CELESTE · 2011 to 2012
$421k
NINDS NIH HHS R21 NS074014
6 · The paper itself

Abstract

Drug and behavioral addictions have overlapping features, e.g., both manifest preference for larger, albeit costlier, reinforcement options in cost/benefit decision-making tasks. Our prior work revealed that the mixed-function serotonergic compound, mirtazapine, attenuates behaviors by rats motivated by abused drugs. To extend this work to behavioral addictions, here we determined if mirtazapine and/or ketanserin, another mixed-function serotonin-acting compound, can alter decision-making in rats that is independent of drug (or food)-motivated reward. Accordingly, we developed a novel variable-ratio task in rats wherein intracranial self-stimulation was used as the positive reinforcer. Using lever pressing for various levels of brain stimulation, the operant task provided choices between a small brain stimulation current delivered on a fixed-ratio schedule (i.e., a predictable reward) and a large brain stimulation delivered following an unpredictable number of responses (i.e., a variable-ratio schedule). This task allowed for demonstration of individualized preference and detection of shifts in motivational influences during a pharmacological treatment. Once baseline preference was established, we determined that pretreatment with mirtazapine or ketanserin significantly decreased preference for the large reinforcer presented after gambling-like schedules of reinforcement. When the rats were tested the next day without drug, preference for the unpredictable large reinforcer option was restored. These data demonstrate that mirtazapine and ketanserin can reduce preference for larger, costlier reinforcement options, and illustrate the potential for these drugs to alter behavior.

Indexed as

Reinforcement ScheduleRewardAnimalsChoice BehaviorDecision MakingGamblingKetanserinMaleMianserinMirtazapineRatsSelf StimulationKetanserinMianserinMirtazapineCost/benefit decision-makingGamblingIntracranial self-stimulationSerotoninVariable-ratio

Identifiers

PMID28412411
PMCPMC5656013
OpenAlexW2606220058

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.