Evidence map›Paper›PMID 29955899›Full record

ArticlePsychopharmacology2018

5-HT

Marina Mori, Iku Tsutsui-Kimura, Masaru Mimura, Kenji F Tanaka

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Which came first: Cannabis use or deficits in impulse control?Progress in neuro-psychopharmacology & biological psychiatry · 2021
    Review
  6. The effect of 5-HTThe journal of physiological sciences : JPS · 2019
    Article
  7. 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

4 authors at 1 institution in 2 countries.

Marina MoriDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Iku Tsutsui-KimuraDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan. ikimura@fas.harvard.edu.
Masaru MimuraDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Kenji F TanakaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan. kftanaka@keio.jp.ORCID http://orcid.org/0000-0003-2511-0057
Keio University · JP

Funding

Ministry of Education, Culture, Sports, Science and Technology 15H03123Ministry of Education, Culture, Sports, Science and Technology 16H01621Ministry of Education, Culture, Sports, Science and Technology 17H06062
6 · The paper itself

Abstract

rationaleImpulsive choice has often been evaluated in rodents according to the proportion of choices for the delayed large magnitude reinforcer (%large choice) in a delay-discounting task (DDT). However, because %large choice is influenced by both sensitivity to reinforcer magnitude and sensitivity to delayed reinforcement (i.e., discounting rate), distinctively evaluating such discounting parameters represents a critical issue demanding methods to determine each parameter in rats. The serotonin (5-HT) system is well known to be involved in impulsive choice; nevertheless, only a few studies have distinguished discounting parameters and investigated how 5-HT modulators affect discounting rate.

objectiveHere, we performed a discounting parameter analysis in mice and examined the effects of various 5-HT modulators on discounting rate.

methodsWe set up DDTs with different delay schedules to determine which schedule could address delay-discounting rates in mice. We examined the effect of the following drugs on impulsive choice: a 5-HT reuptake inhibitor (paroxetine), a 5-HT

resultsMice showed typical delay discounting at the shorter delay schedules (up to 4 s delay). The %large choice under shorter, but not longer, schedules followed an exponential function and allowed us to derive discounting rates. We selected a DDT with a 4-s delay schedule for further experiments. Granisetron and ondansetron, but not paroxetine or 8-OH-DPAT, decreased discounting rates without affecting sensitivity to reinforcer magnitude.

conclusionWe found that a method to calculate discounting rates in rats is also applicable to mouse models. We also provided evidence that 5-HT

Indexed as

Reinforcement, PsychologyRewardAnimalsChoice BehaviorConditioning, OperantDelay DiscountingImpulsive BehaviorMaleMiceMice, Inbred C57BLRatsSerotonin 5-HT3 Receptor AntagonistsSerotonin 5-HT3 Receptor AntagonistsDelay discounting taskExponential functionGranisetronImpulsive choiceOndansetronSerotonin

Identifiers

PMID29955899
OpenAlexW2810248206

What OpenQuestion holds

Textmetadata
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.