Evidence map›Paper›PMID 39528410›Full record

ArticleThe European journal of neuroscience2024

Ketone ester-enriched diet ameliorates motor and dopamine release deficits in MitoPark mice.

Vikrant R Mahajan, Jacob A Nadel, M Todd King, Robert J Pawlosky, Margaret I Davis, Richard L Veech, David M Lovinger, Armando G Salinas

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
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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

8 authors.

Vikrant R MahajanLaboratory for Integrative Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, USA.
Jacob A NadelLaboratory for Integrative Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, USA.
M Todd KingLaboratory for Metabolic Control, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, USA.
Robert J PawloskyLaboratory for Metabolic Control, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, USA.
Margaret I DavisLaboratory for Integrative Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, USA.
Richard L VeechLaboratory for Metabolic Control, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, USA.
David M LovingerLaboratory for Integrative Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, USA.
Armando G SalinasLaboratory for Integrative Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, USA.ORCID 0000-0002-1682-128X

Funding

Chronic ethanol effects on cholinergic interneurons of the striatumR00AA025991 · NIAAA · LOUISIANA STATE UNIV HSC SHREVEPORT · PI SALINAS, ARMANDO · 2022 to 2024
$747k
Chronic ethanol effects on cholinergic interneurons of the striatumK99AA025991 · NIAAA · GEORGE MASON UNIVERSITY · PI SALINAS, ARMANDO · 2018 to 2020
$287k
Impact of chronic alcohol on neuronal cholinergic signalingR03AA030400 · NIAAA · LOUISIANA STATE UNIV HSC SHREVEPORT · PI SALINAS, ARMANDO · 2023 to 2023
$146k
NIAAA NIH HHS AA000110NIAAA NIH HHS AA000407NIAAA NIH HHS AA025991NIAAA NIH HHS AA030400NIAAA NIH HHS K99 AA025991NIAAA NIH HHS R00 AA025991NIAAA NIH HHS R03 AA030400
6 · The paper itself

Abstract

Parkinson's disease (PD) is a progressive, neurodegenerative disease characterized by motor dysfunction and dopamine deficits. The MitoPark (MP) mouse model of PD recapitulates several facets of Parkinson's disease, including gradual development of motor deficits, which enables the study of potential therapeutic interventions. One therapeutic strategy involves decreasing the mitochondrial metabolic load by inducing ketosis and providing an alternative energy source for neurons, leading to decreased neuronal oxidative stress. Thus, we hypothesized that administration of a ketone ester-enriched diet (KEED) would improve motor and dopamine release deficits in MP mice. Motor function (rotarod and open field tests), dopamine release (fast-scan cyclic voltammetry), tissue dopamine levels (gas chromatography-mass spectrometry) and dopamine neurons and axons (immunofluorescence) were assessed in MP, and control mice fed either the standard or a KEED. When started on the ketone diet before motor dysfunction onset, MP mice had improved motor function relative to standard diet (SD) MP mice. While the KEED did not preserve dopamine neurons or striatal dopamine axons, dopamine release in ketone diet MP mice was greater than SD MP mice but less than control mice. In a follow-up experiment, we began the ketone diet after motor dysfunction onset and observed a modest preservation of motor function in ketone diet MP mice relative to SD MP mice. The improvement in motor dysfunction indicates that a KEED or ketone supplement may have a beneficial effect on delaying motor deficit progression in Parkinson's disease.

Indexed as

DopamineDopaminergic NeuronsKetonesAnimalsCorpus StriatumDiet, KetogenicDisease Models, AnimalEstersMaleMiceMice, Inbred C57BLMice, TransgenicMotor ActivityParkinson DiseaseDopamineEstersKetonesdopamine neuronsketosisneuroprotectionParkinson's diseasestriatum

Identifiers

PMID39528410
PMCPMC11612846

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Registered trials

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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.