Evidence map›Paper›PMID 39843219›Full record

ArticleBritish journal of pharmacology2025

Cardiovascular and locomotor effects of binary mixtures of common 'bath salts' constituents: Studies with methylone, methylenedioxypyrovalerone and caffeine in rats.

Robert W Seaman, David G Galindo, Benjamin T Stinson, Agnieszka Sulima, Kenner C Rice, Martin A Javors, Brett C Ginsburg, Gregory T Collins

Abstract read
In one paragraph

Article in British journal of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Robert W SeamanDepartment of Pharmacology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
David G GalindoDepartment of Psychiatry and Behavioral Sciences, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Benjamin T StinsonDepartment of Psychiatry and Behavioral Sciences, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Agnieszka SulimaDrug Design and Synthesis Section, Molecular Targets and Medications Discovery Branch, NIDA and NIAAA, Bethesda, Maryland, USA.
Kenner C RiceDrug Design and Synthesis Section, Molecular Targets and Medications Discovery Branch, NIDA and NIAAA, Bethesda, Maryland, USA.
Martin A JavorsDepartment of Psychiatry and Behavioral Sciences, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Brett C GinsburgDepartment of Psychiatry and Behavioral Sciences, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Gregory T CollinsDepartment of Pharmacology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.

Funding

Bath Salts: Abuse-related and Toxic EffectsR01DA039146 · NIDA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Gregory Collins · 2015 to 2026
$4.0M
Cognitive flexibility as a target for relapse preventionR01AA025664 · NIAAA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI GINSBURG, BRETT C · 2018 to 2022
$1.7M
Intramural Research Program, National Institute on Drug Abuse and National Institute of Alcohol Abuse and Alcoholism (KCR)NIAAA NIH HHS R01 AA025664NIAAA NIH HHS R01AA025664 (BCG)NIDA NIH HHS 1ZIADA000527NIDA NIH HHS R01 DA039146NIDA NIH HHS R01DA039146 (GTC)
6 · The paper itself

Abstract

background and purposeThe use of 'bath salts' drug preparations has been associated with high rates of toxicity and death. Preparations often contain mixtures of drugs, including multiple synthetic cathinones or synthetic cathinones and caffeine. Little is known about the interactions of 'bath salts' constituents and adverse effects often reported by users. EXPERIMENTAL APPROACH: This study used adult male Sprague-Dawley rats to characterise the cardiovascular effects, locomotor effects and pharmacokinetics of methylone, methylenedioxypyrovalerone (MDPV) and caffeine, administered alone and as binary mixtures. Dose-addition analyses were used to determine the effect levels of a strictly additive interaction for dose pairs. KEY

resultsMethylone, MDPV and caffeine increased heart rate (HR) and locomotion, with methylone producing the largest increase in HR, MDPV producing the largest increase in locomotor activity and caffeine being the least effective in stimulating HR and locomotor activity. MDPV and caffeine increased mean arterial pressure (MAP), with caffeine being more effective than MDPV. The nature of the interactions between methylone and MDPV tended towards sub-additivity for all endpoints, whereas interactions between MDPV or methylone and caffeine tended to be additive or sub-additive for cardiovascular endpoints, and additive or supra-additive for increases in locomotion. No pharmacokinetic interactions were observed between individual constituents, but methylone appeared to display nonlinear pharmacokinetics at the largest dose evaluated. CONCLUSION AND IMPLICATIONS: These findings demonstrate that 'bath salts' preparations can impact both cardiovascular and locomotor effects and suggest that interactions among constituent drugs could contribute to the 'bath salts' toxidrome reported by human users.

Indexed as

BenzodioxolesCaffeineLocomotionMethamphetaminePyrrolidinesAnimalsBlood PressureCentral Nervous System StimulantsDose-Response Relationship, DrugHeart RateMaleRatsRats, Sprague-DawleySynthetic CathinoneBenzodioxolesCaffeineCentral Nervous System StimulantsMethamphetaminemethylonePyrrolidinesSynthetic Cathinonebath saltscaffeineMDPVmethylonepolysubstance usesynthetic cathinones

Identifiers

PMID39843219
PMCPMC12183792

What Socratic 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 Socratic graph.