Evidence map›Paper›PMID 28705715›Full record

ArticleBrain research2017

Acute treatment with doxorubicin affects glutamate neurotransmission in the mouse frontal cortex and hippocampus.

Theresa Currier Thomas, Joshua A Beitchman, Francois Pomerleau, Teresa Noel, Paiboon Jungsuwadee, D Allan Butterfield, Daret K St Clair, Mary Vore, Greg A Gerhardt

Open access · greenAbstract read
In one paragraph

Article in Brain research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 55 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Theresa Currier ThomasSpinal Cord & Brain Injury Research Center, University of Kentucky College of Medicine, Lexington, KY 40536, USA; Barrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ 85016, USA; Department of Child Health, University of Arizona College of Medicine, Phoenix, AZ 85004, USA; Phoenix VA Health Care System, Phoenix, AZ 85012, USA. Electronic address: theresathomas@email.arizona.edu.
Joshua A BeitchmanDepartment of Child Health, University of Arizona College of Medicine, Phoenix, AZ 85004, USA; Phoenix VA Health Care System, Phoenix, AZ 85012, USA; Midwestern University, Glendale, AZ 85308, USA.
Francois PomerleauDepartments of Neuroscience, Neurology, Neurosurgery, Psychiatry and Electrical Engineering, University of Kentucky College of Medicine, Lexington, KY 40536, USA; Center for Microelectrode Technology, University of Kentucky College of Medicine, Lexington, KY 40536, USA; Brain Research Center, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
Teresa NoelDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
Paiboon JungsuwadeeDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40536, USA; School of Pharmacy & Health Sciences, Fairleigh Dickinson University, Florham Park, NJ 07932, USA.
D Allan ButterfieldDepartment of Chemistry, Redox Chemistry and Biology Core, Markey Cancer, and Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY 40506, USA.
Daret K St ClairDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
Mary VoreDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
Greg A GerhardtSpinal Cord & Brain Injury Research Center, University of Kentucky College of Medicine, Lexington, KY 40536, USA; Departments of Neuroscience, Neurology, Neurosurgery, Psychiatry and Electrical Engineering, University of Kentucky College of Medicine, Lexington, KY 40536, USA; Center for Microelectrode Technology, University of Kentucky College of Medicine, Lexington, KY 40536, USA; Brain Research Center, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
University of Kentucky · USBarrow Neurological Institute · USMidwestern University · US

Funding

KENTUCKY CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCEUL1RR033173 · NCRR · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2011 to 2011
$3.5M
THE MOLECULAR AND CELLULAR BASIS OF BRAIN AGINGT32AG000242 · NIA · UNIVERSITY OF KENTUCKY · PI GERHARDT, GREG A. · 1994 to 2013
$3.4M
The role of MRP1 in Protection of Cardiac InjuryR01CA139844 · NCI · UNIVERSITY OF KENTUCKY · PI VORE, MARY · 2008 to 2012
$1.3M
MbSOD in chemotherapeutic-Induced Cardiac InjuryR01CA139843 · NCI · UNIVERSITY OF KENTUCKY · PI ST CLAIR, DARET K · 2008 to 2012
$1.3M
NCI NIH HHS R01 CA139843NCI NIH HHS R01 CA139844NCRR NIH HHS UL1 RR033173NIA NIH HHS T32 AG000242
6 · The paper itself

Abstract

Doxorubicin (DOX) is a potent chemotherapeutic agent known to cause acute and long-term cognitive impairments in cancer patients. Cognitive function is presumed to be primarily mediated by neuronal circuitry in the frontal cortex (FC) and hippocampus, where glutamate is the primary excitatory neurotransmitter. Mice treated with DOX (25mg/kg i.p.) were subjected to in vivo recordings under urethane anesthesia at 24h post-DOX injection or 5 consecutive days of cognitive testing (Morris Water Maze; MWM). Using novel glutamate-selective microelectrode arrays, amperometric recordings measured parameters of extracellular glutamate clearance and potassium-evoked release of glutamate within the medial FC and dentate gyrus (DG) of the hippocampus. By 24h post-DOX injection, glutamate uptake was 45% slower in the FC in comparison to saline-treated mice. In the DG, glutamate took 48% longer to clear than saline-treated mice. Glutamate overflow in the FC was similar between treatment groups, however, it was significantly increased in the DG of DOX treated mice. MWM data indicated that a single dose of DOX impaired swim speed without impacting total length traveled. These data indicate that systemic DOX treatment changes glutamate neurotransmission in key nuclei associated with cognitive function within 24h, without a lasting impact on spatial learning and memory. Understanding the functional effects of DOX on glutamate neurotransmission may help us understand and prevent some of the debilitating side effects of chemotherapeutic treatment in cancer survivors.

Indexed as

AnimalsCognitionDentate GyrusDoxorubicinFrontal LobeGlutamic AcidHippocampusMaleMaze LearningMemoryMiceSpatial LearningSynaptic TransmissionTemporal LobeDoxorubicinGlutamic AcidAmperometryChemobrainDentate gyrusDoxorubicinGlutamate clearancePrefrontal cortex

Identifiers

PMID28705715
PMCPMC5576558
OpenAlexW2734595528

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.