Evidence map›Paper›PMID 21190217›Full record

ArticleSynapse (New York, N.Y.)2011

Methamphetamine treatment during development attenuates the dopaminergic deficits caused by subsequent high-dose methamphetamine administration.

Lisa M McFadden, Amanda J Hoonakker, Paula L Vieira-Brock, Kristen A Stout, Nicole M Sawada, Jonathan D Ellis, Scott C Allen, Elliot T Walters, Shannon M Nielsen, James W Gibb and 4 more

Open access · greenAbstract read
In one paragraph

Article in Synapse (New York, N.Y.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Peri-adolescent exposure to (meth)amphetamine in animal models.International review of neurobiology · 2022
    Review
  2. Article
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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

14 authors at 1 institution in 1 country.

Lisa M McFaddenDepartment of Pharmacology and Toxicology, University of Utah, Salt Lake City, Utah 84112, USA. lisa.mcfadden@utah.edu
Amanda J Hoonakker
Paula L Vieira-Brock
Kristen A Stout
Nicole M Sawada
Jonathan D Ellis
Scott C Allen
Elliot T Walters
Shannon M Nielsen
James W Gibb
Mario E Alburges
Diana G Wilkins
Glen R Hanson
Annette E Fleckenstein
University of Utah · US

Funding

Vmat AND NEUROTOXICITYP01DA013367 · NIDA · UNIVERSITY OF UTAH · PI CROUCH, DENNIS J. · 2001 to 2012
$10.1M
DRUG ABUSE &REGULATORY ENZYMES OF BIOGENIC AMINESR01DA000869 · NIDA · UNIVERSITY OF UTAH · PI FLECKENSTEIN, ANNETTE · 1985 to 2010
$2.9M
Psychostimulants and Monoamine TransportersR01DA011389 · NIDA · UNIVERSITY OF UTAH · PI FLECKENSTEIN, ANNETTE · 2003 to 2012
$2.5M
NEUROCHEMICAL ALTERATIONS BY DESIGNER DRUGSR01DA004222 · NIDA · UNIVERSITY OF UTAH · PI HANSON, GLEN R · 1986 to 2010
$2.0M
K02 ApplicationK02DA019447 · NIDA · UNIVERSITY OF UTAH · PI FLECKENSTEIN, ANNETTE · 2005 to 2014
$1.3M
Pharmacology and Toxicology of Methamphetamine Abuse (K05 DA00378)K05DA000378 · NIDA · UNIVERSITY OF UTAH · PI HANSON, GLEN R · 1998 to 2011
$1.2M
METHAMPHETAMINE AND DOPAMINE TRANSPORTERSR29DA011389 · NIDA · UNIVERSITY OF UTAH · PI FLECKENSTEIN, ANNETTE · 1998 to 2002
$329k
NIDA NIH HHS DA00378NIDA NIH HHS DA00869NIDA NIH HHS DA013367NIDA NIH HHS DA019447NIDA NIH HHS DA04222NIDA NIH HHS DA11389NIDA NIH HHS K02 DA019447NIDA NIH HHS K05 DA000378NIDA NIH HHS P01 DA013367NIDA NIH HHS R01 DA000869NIDA NIH HHS R01 DA004222NIDA NIH HHS R01 DA011389NIDA NIH HHS R29 DA011389
6 · The paper itself

Abstract

Administration of high doses of methamphetamine (METH) causes persistent dopaminergic deficits in both nonhuman preclinical models and METH-dependent persons. Noteworthy, adolescent [i.e., postnatal day (PND) 40] rats are less susceptible to this damage than young adult (PND90) rats. In addition, biweekly treatment with METH, beginning at PND40 and continuing throughout development, prevents the persistent dopaminergic deficits caused by a "challenge" high-dose METH regimen when administered at PND90. Mechanisms underlying this "resistance" were thus investigated. Results revealed that biweekly METH treatment throughout development attenuated both the acute and persistent deficits in VMAT2 function, as well as the acute hyperthermia, caused by a challenge METH treatment. Pharmacokinetic alterations did not appear to contribute to the protection afforded by the biweekly treatment. Maintenance of METH-induced hyperthermia abolished the protection against both the acute and persistent VMAT2-associated deficits suggesting that alterations in thermoregulation were caused by exposure of rats to METH during development. These findings suggest METH during development prevents METH-induced hyperthermia and the consequent METH-related neurotoxicity.

Indexed as

AnimalsBody Temperature RegulationBrainCentral Nervous System StimulantsChromatography, GasDopamineFeverGrowth and DevelopmentMaleMass SpectrometryMethamphetamineRatsRats, Sprague-DawleyVesicular Monoamine Transport ProteinsCentral Nervous System StimulantsDopamineMethamphetamineSlc18a2 protein, ratVesicular Monoamine Transport Proteins

Identifiers

PMID21190217
PMCPMC3908924
OpenAlexW2157570964

What OpenQuestion 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 OpenQuestion graph.