Evidence map›Paper›PMID 38496609›Full record

ArticlebioRxiv : the preprint server for biology2024

Effects of access condition on substance use disorder-like phenotypes in male and female rats self-administering MDPV or cocaine.

Michelle R Doyle, Nina M Beltran, Mark S A Bushnell, Maaz Syed, Valeria Acosta, Marisa Desai, Kenner C Rice, Katherine M Serafine, Georgianna G Gould, Lynette C Daws and 1 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Michelle R DoyleDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Nina M BeltranDepartment of Psychology, University of Texas at El Paso, El Paso, TX, USA.
Mark S A BushnellDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Maaz SyedDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Valeria AcostaDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Marisa DesaiDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Kenner C RiceDrug Design and Synthesis Section, Molecular Targets and Medications Discovery Branch National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism - Intramural Research Program, Bethesda, MD.
Katherine M SerafineDepartment of Psychology, University of Texas at El Paso, El Paso, TX, USA.
Georgianna G GouldDepartment of Cellular and Integrative Physiology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Lynette C DawsDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Gregory T CollinsDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
The University of Texas Health Science Center at San Antonio · USThe University of Texas at El Paso · USNational Institute on Drug Abuse · US

Funding

Bath Salts: Abuse-related and Toxic EffectsR01DA039146 · NIDA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Gregory Collins · 2015 to 2026
$4.0M
Uptake2 transporters: Novel sex-dependent molecular targets to treat stimulant use disorderR01DA055703 · NIDA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LYNETTE C DAWS · 2023 to 2026
$2.7M
Medicinal Chemistry of Drugs Acting on Central and Peripheral Opioid ReceptorsZ01DA000527 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI RICE, KENNER · 2008 to 2008
$2.1M
Integrated Graduate Training Program in Neuroscience, UTHSCSAT32NS082145 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI David A Morilak · 2013 to 2026
$1.5M
Exploring a role for organic transporter 3 in the mechanism of action of drugs of abuseR21DA046044 · NIDA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI DAWS, LYNETTE C, KOEK, WOUTER · 2018 to 2019
$419k
Role of dopamine D3 and serotonin 2C receptors in the development of an addiction-like phenotype in ratsR36DA050955 · NIDA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI DOYLE, MICHELLE RIANE · 2020 to 2021
$108k
Intramural NIH HHS Z01 DA000527NIDA NIH HHS R01 DA039146NIDA NIH HHS R01 DA055703NIDA NIH HHS R21 DA046044NIDA NIH HHS R36 DA050955NINDS NIH HHS T32 NS082145
6 · The paper itself

Abstract

Substance use disorder (SUD) is a heterogeneous disorder, where severity, symptoms, and patterns of substance use vary across individuals. Yet, when rats are allowed to self-administer drugs such as cocaine under short-access conditions, their behavior tends to be well-regulated and homogeneous in nature; though individual differences can emerge when rats are provided long- or intermittent-access to cocaine. In contrast to cocaine, significant individual differences emerge when rats are allowed to self-administer 3,4-methylenedioxypyrovalerone (MDPV), even under short-access conditions, wherein ~30% of rats rapidly transition to high levels of drug-taking. This study assessed the SUD-like phenotypes of male and female Sprague Dawley rats self-administering MDPV (0.032 mg/kg/infusion) or cocaine (0.32 mg/kg/infusion) by comparing level of drug intake, responding during periods of signaled drug unavailability, and sensitivity to footshock punishment to test the hypotheses that: (1) under short-access conditions, rats that self-administer MDPV will exhibit a more robust SUD-like phenotype than rats that self-administered cocaine; (2) female rats will have a more severe phenotype than male rats; and (3) compared to short-access, long- and intermittent-access to MDPV or cocaine self-administration will result in a more robust SUD-like phenotype. After short-access, rats that self-administered MDPV exhibited a more severe phenotype than rats that self-administered cocaine. Though long- and intermittent-access to cocaine and MDPV self-administration altered drug-taking patterns, manipulating access conditions did not systematically alter their SUD-like phenotype. Evidence from behavioral and quantitative autoradiography studies suggest that these differences are unlikely due to changes in expression levels of dopamine transporter, dopamine D

Identifiers

PMID38496609
PMCPMC10942381
OpenAlexW4392603621

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.