Evidence map›Paper›PMID 40932492›Full record

ArticlePsychopharmacology2026

Effects of psychostimulants on locomotor activity in the BTBR T

William E Fantegrossi, Hannah E Shaw, Stephen A Fagot, Kamryn Thomas, Harpreet Kaur

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Article in Psychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

William E FantegrossiDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 638, Little Rock, AR, 72205, USA. WEFantegrossi@uams.edu.ORCID http://orcid.org/0000-0001-9964-1593
Hannah E ShawDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 638, Little Rock, AR, 72205, USA.
Stephen A FagotCollege of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Kamryn ThomasDepartment of Neuroscience, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Harpreet KaurPharmAla Biotech, Inc, Toronto, ON, Canada.

Funding

NIDA NIH HHS DA022981
6 · The paper itself

Abstract

rationalePeople with autism spectrum disorder (ASD) often have psychiatric comorbidities, with attention deficit hyperactivity disorder (ADHD) being the most common. Psychostimulants used as ADHD treatments are less effective in these dual diagnosis individuals, with lower rates of symptom improvement and a higher incidence of adverse drug effects. The mutant BTBR T

objectivesWe determined dose-effect curves for locomotor effects of 10 different psychostimulants in adult male BTBR and C57Bl/6 N (C57) mice, including amphetamine and other monoamine releasers, methylphenidate and other reuptake inhibitors, as well as some drugs with a mixed profile of monoamine release and reuptake inhibition.

methodsMice were surgically implanted with radiotelemetry probes which measured locomotor activity within the home cage.

resultsA robust strain difference was typically observed at large doses, wherein C57 mice entered motor stereotypy while BTBRs did not. This resistance to stereotypy in BTBR mice resulted in dramatically increased locomotor stimulant effects across drugs.

conclusionsBecause resistance to locomotor stereotypy in BTBRs was observed among psychostimulants with distinct mechanisms of action and selectivities for monoamine transporters, it is likely that pervasive neurobiological and/or metabolic differences in BTBR mice mediate this effect. Further studies to determine the mechanisms underlying the exaggerated locomotor responses to psychostimulants in BTBR mice are needed. Results of these studies may guide drug development efforts toward identifying more effective and better-tolerated medications for comorbid ASD with ADHD.

Indexed as

Attention Deficit Disorder with HyperactivityAutism Spectrum DisorderCentral Nervous System StimulantsLocomotionMotor ActivityAmphetamineAnimalsComorbidityDisease Models, AnimalDose-Response Relationship, DrugMaleMethylphenidateMiceMice, Inbred C57BLAmphetamineCentral Nervous System StimulantsMethylphenidateAttention deficit hyperactivity disorderAutismLocomotor activityMousePsychostimulants

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Read underepoch 390

Registered trials

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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.