Evidence map›Paper›PMID 40368903›Full record

ArticleNature communications2025

Intermittent fasting reduces alpha-synuclein pathology and functional decline in a mouse model of Parkinson's disease.

Éva M Szegő, Lennart Höfs, Anna Antoniou, Elisabeth Dinter, Nadine Bernhardt, Anja Schneider, Donato A Di Monte, Björn H Falkenburger

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Cellular and systemic modifiers of alpha-synuclein proteostasis.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
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  7. NADAlzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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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.

Éva M SzegőDepartment of Neurology, TU Dresden, Dresden, Germany. eva.szego@gmail.com.ORCID http://orcid.org/0000-0002-2629-2131
Lennart HöfsDepartment of Neurology, TU Dresden, Dresden, Germany.
Anna AntoniouDepartment of Old Age Psychiatry and Cognitive Disorders, University Hospital Bonn, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-3907-2330
Elisabeth DinterDepartment of Neurology, TU Dresden, Dresden, Germany.ORCID http://orcid.org/0009-0008-9467-6402
Nadine BernhardtDepartment of Psychiatry and Psychotherapy, TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-3188-8431
Anja SchneiderGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.ORCID http://orcid.org/0000-0001-9540-8700
Donato A Di MonteGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.ORCID http://orcid.org/0000-0002-8296-836X
Björn H FalkenburgerDepartment of Neurology, TU Dresden, Dresden, Germany. bfalken@ukdd.de.ORCID http://orcid.org/0000-0002-2387-526X

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) FA-658-3-1
6 · The paper itself

Abstract

Parkinson's disease (PD) is a neurodegenerative disorder characterized by dopaminergic neuron degeneration and α-synuclein (aSyn) accumulation. Environmental factors play a significant role in PD progression, highlighting the potential of non-pharmacological interventions. This study investigates the therapeutic effects of intermittent fasting (IF) in an rAAV-aSyn mouse model of PD. IF, initiated four weeks post-induction of aSyn pathology, improved motor function and reduced dopaminergic neuron and axon terminal degeneration. Additionally, IF preserved dopamine levels and synaptic integrity in the striatum. Mechanistically, IF enhanced autophagic activity, promoting phosphorylated-aSyn clearance and reducing its accumulation in insoluble brain fractions. Transcriptome analysis revealed IF-induced modulation of inflammation-related genes and microglial activation. Validation in primary cultures confirmed that autophagy activation and inflammatory modulators (CCL17, IL-36RN) mitigate aSyn pathology. These findings suggest that IF exerts neuroprotective effects, supporting further exploration of IF and IF-mimicking therapies as potential PD treatments.

Indexed as

alpha-SynucleinFastingParkinson DiseaseAnimalsAutophagyCorpus StriatumDisease Models, AnimalDopamineDopaminergic NeuronsHumansIntermittent FastingMaleMiceMice, Inbred C57BLMicrogliaalpha-SynucleinDopamine

Identifiers

PMID40368903
PMCPMC12078643

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.