Evidence map›Paper›PMID 33449137›Full record

ArticlePsychopharmacology2021

Effects of clonidine on progressive ratio schedule performance in Fmr1 knockout mice.

Craige C Wrenn, Eric French, Dustin Baker, Randall McCallian, Ryan Kirk, Mark P Reilly, Maria G Valdovinos

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Maternal immune activation in mice recapitulates features of attention-deficit/hyperactivity disorder (ADHD) in susceptible offspring.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    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

7 authors at 2 institutions in 1 country.

Craige C WrennCollege of Pharmacy and Health Sciences, Drake University, 2507 University Ave, Des Moines, IA, 50311, USA. craige.wrenn@drake.edu.
Eric FrenchPsychology Department, Central Michigan University, East Campus Dr, Mount Pleasant, MI, 48858, USA.
Dustin BakerPsychology Department, Drake University, 2507 University Ave, Des Moines, IA, 50311, USA.
Randall McCallianPsychology Department, Drake University, 2507 University Ave, Des Moines, IA, 50311, USA.
Ryan KirkPsychology Department, Drake University, 2507 University Ave, Des Moines, IA, 50311, USA.
Mark P ReillyPsychology Department, Central Michigan University, East Campus Dr, Mount Pleasant, MI, 48858, USA.
Maria G ValdovinosPsychology Department, Drake University, 2507 University Ave, Des Moines, IA, 50311, USA.
Drake University · USCentral Michigan University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleFragile X syndrome (FXS), the most prevalent genetic form of intellectual disability, is characterized by intellectual impairment, impaired sociability, aggression, self-injury, hyperactivity, and attention deficits. A consequence of the hyperactivity and attention deficits is that individuals with FXS are frequently diagnosed with attention deficit hyperactivity disorder (ADHD) and treated with medications approved for ADHD (e.g., the α

objectivesIn the present progressive ratio study, we used a knockout mouse model to test the effects of the fragile X genotype, the α

resultsWe found that clonidine decreased the progressive ratio breakpoint, increased the length of post-reinforcement pauses, and slowed the run rate. None of these effects varied by genotype. The effect on breakpoint suggests that clonidine alters motivation, but analysis using mathematical principles of reinforcement (MPR) did not rule out motor parameters as a contributor.

conclusionsOur findings show that clonidine alters operant behavior and serve as a caution for combining clonidine with behavioral therapies that rely on positive reinforcement. Further research using different murine behaviors (e.g., touchscreen tasks) or different animal models (e.g., knockout rats) is needed to explore the interaction between pharmaco- and behavioral therapy.

Indexed as

Reinforcement ScheduleAdrenergic alpha-2 Receptor AgonistsAnimalsClonidineConditioning, OperantFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeGenotypeMaleMiceMice, Inbred C57BLMice, KnockoutMotivationRewardAdrenergic alpha-2 Receptor AgonistsClonidineFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1BreakpointClonidineFragile XOperantReward

Identifiers

PMID33449137
OpenAlexW3119208427

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.