Evidence map›Paper›PMID 22115899›Full record

ArticleNeuropharmacology2012

Methamphetamine-induced changes in the object recognition memory circuit.

Carmela M Reichel, Lauren A Ramsey, Marek Schwendt, Jacqueline F McGinty, Ronald E See

Open access · greenAbstract read
In one paragraph

Article in Neuropharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

54 citing papers in PubMed, 108 citations in OpenAlex.

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  9. Repeated methamphetamine administration produces cognitive deficits through augmentation of GABAergic synaptic transmission in the prefrontal cortex.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
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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

5 authors at 1 institution in 1 country.

Carmela M ReichelDepartment of Neurosciences, Medical University of South Carolina, 173 Ashley Avenue, Charleston, SC 29425, USA. reichel@musc.edu
Lauren A Ramsey
Marek Schwendt
Jacqueline F McGinty
Ronald E See
Medical University of South Carolina · US

Funding

Corticostriatal Neuroplasticity and Cognition in Methamphetamine AddictionR01DA033049 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SCOFIELD, MICHAEL DAVID · 2012 to 2022
$3.4M
Translational Research in Addiction CenterP20DA022658 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SEE, RONALD E · 2006 to 2009
$3.0M
MUSC FACIL EXPANSION &RENOV: SLE C06RR015455 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CROUCH, ROSALIE K · 2002 to 2002
$2.0M
Reversal of Methamphetamine Induced Cognitive Deficits and mGlu ReceptorsF32DA029344 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI REICHEL, CARMELA M · 2010 to 2011
$63k
NCRR NIH HHS C06 RR015455NIDA NIH HHS F32 DA029344NIDA NIH HHS F32DA029344NIDA NIH HHS P20 DA022658NIDA NIH HHS P20DA022658NIDA NIH HHS R01 DA033049
6 · The paper itself

Abstract

Chronic methamphetamine (meth) can lead to persisting cognitive deficits in human addicts and animal models of meth addiction. Here, we examined the impact of either contingent or non-contingent meth on memory performance using an object-in-place (OIP) task, which measures the ability to detect an object relative to its location and surrounding objects. Further, we quantified monoamine transporter levels and markers of neurotoxicity within the OIP circuitry and striatum. Male Long-Evans rats received an acute meth binge (4 × 4 mg/kg i.p., 2 h intervals) or self-administered meth (0.02 mg/infusion, i.v.; 7 days for 1 h/day, followed by 14 days for 6 h/day). Rats were tested for OIP recognition memory following one week of withdrawal. Subsequently, transporters for serotonin (SERT) and norepinephrine (NET) were quantified using Western blot in tissue obtained from the hippocampus, perirhinal cortex, and prefrontal cortex. In addition, striatal dopamine transporters, tyrosine hydroxylase, and glial fibrillary acidic protein were measured to assess potential neurotoxicity. Control (saline-treated) rats spent more time interacting with the objects in the changed locations. In contrast, contingent or non-contingent meth resulted in disrupted OIP performance as seen by similar amounts of time spent with all objects, regardless of location. While only acute meth binge produced signs of neurotoxicity, both meth regimens decreased SERT in the perirhinal cortex and hippocampus. Only meth self-administration resulted in a selective decrease in NET. Meth-induced changes in SERT function in the OIP circuitry may underlie memory deficits independently of overt neurotoxic effects. This article is part of a Special Issue entitled 'Post-Traumatic Stress Disorder'.

Indexed as

AnimalsCorpus StriatumDopamine Plasma Membrane Transport ProteinsDopamine Uptake InhibitorsGlial Fibrillary Acidic ProteinHippocampusMaleMethamphetamineNorepinephrine Plasma Membrane Transport ProteinsPrefrontal CortexRatsRats, Long-EvansRecognition, PsychologySelf AdministrationSerotonin Plasma Membrane Transport ProteinsDopamine Plasma Membrane Transport ProteinsDopamine Uptake InhibitorsGlial Fibrillary Acidic ProteinMethamphetamineNorepinephrine Plasma Membrane Transport ProteinsSerotonin Plasma Membrane Transport Proteins

Identifiers

PMID22115899
PMCPMC3262904
OpenAlexW2132622783

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.