Evidence map›Paper›PMID 26644333›Full record

ArticleNeuroscience letters2016

Long-term effect of sub-anesthetic ketamine in reducing L-DOPA-induced dyskinesias in a preclinical model.

Mitchell J Bartlett, Ria M Joseph, Lindsey M LePoidevin, Kate L Parent, Nicholas D Laude, Levi B Lazarus, Michael L Heien, Miguel Estevez, Scott J Sherman, Torsten Falk

Abstract read
In one paragraph

Article in Neuroscience letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

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  16. Roles of Glutamate Receptors in Parkinson's Disease.International journal of molecular sciences · 2019
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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

10 authors at 1 institution in 1 country.

Mitchell J BartlettDepartment of Neurology, University of Arizona, Tucson, AZ, USA.
Ria M JosephDepartment of Neurology, University of Arizona, Tucson, AZ, USA.
Lindsey M LePoidevinDepartment of Neurology, University of Arizona, Tucson, AZ, USA.
Kate L ParentDepartment of Chemistry & Biochemistry, University of Arizona, Tucson, AZ, USA.
Nicholas D LaudeDepartment of Chemistry & Biochemistry, University of Arizona, Tucson, AZ, USA.
Levi B LazarusDepartment of Chemistry & Biochemistry, University of Arizona, Tucson, AZ, USA.
Michael L HeienDepartment of Chemistry & Biochemistry, University of Arizona, Tucson, AZ, USA.
Miguel EstevezNeurometrica, LLC, Eugene, OR, USA.
Scott J ShermanDepartment of Neurology, University of Arizona, Tucson, AZ, USA.
Torsten FalkDepartment of Neurology, University of Arizona, Tucson, AZ, USA. Electronic address: tfalk@u.arizona.edu.
University of Arizona · US

Funding

CHEMISTRY-BIOLOGY INTERFACE TRAINING PROGRAMT32GM008804 · NIGMS · UNIVERSITY OF ARIZONA · PI MONTFORT, WILLIAM R. · 2003 to 2023
$3.9M
NIGMS NIH HHS T32-GM00804NIGMS NIH HHS T32 GM008804
6 · The paper itself

Abstract

Low-dose sub-anesthetic ketamine infusion treatment has led to a long-term reduction of treatment-resistant depression and posttraumatic stress disorder (PTSD) symptom severity, as well as reduction of chronic pain states, including migraine headaches. Ketamine also is known to change oscillatory electric brain activity. One commonality between migraine headaches, depression, PTSD, Parkinson's disease (PD) and l-DOPA-induced dyskinesias (LID) is hypersynchrony of electric activity in the brain, including the basal ganglia. Therefore, we investigated the use of low-dose sub-anesthetic ketamine in the treatment of LID. In a preclinical rodent model of LID, ketamine (5-20mg/kg) led to long-term dose-dependent reduction of abnormal involuntary movements, only when low-dose ketamine was given for 10h continuously (5× i.p. injections two hours apart) and not after a single acute low-dose ketamine i.p. injection. Pharmacokinetic analysis of plasma levels showed ketamine and its major metabolites were not detectable any more at time points when a lasting anti-dyskinetic effect was seen, indicating a plastic change in the brain. This novel use of low-dose sub-anesthetic ketamine infusion could lead to fast clinical translation, and since depression and comorbid pain states are critical problems for many PD patients could open up the road to a new dual therapy for patients with LID.

Indexed as

AnimalsAntiparkinson AgentsDose-Response Relationship, DrugDyskinesia, Drug-InducedKetamineLevodopaMaleRats, Sprague-DawleyReceptors, N-Methyl-D-AspartateReceptors, OpioidTime FactorsAntiparkinson AgentsKetamineLevodopaReceptors, N-Methyl-D-AspartateReceptors, OpioidHypersynchronyNMDA ReceptorsOpioid receptorsParkinson’s diseasePreclinical rodent model

Identifiers

PMID26644333
PMCPMC4728020
OpenAlexW2173305081

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.