ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
Neuroprotective Effects of Time-Restricted Feeding Combined With Different Protein Sources in MPTP-Induced Parkinson's Disease Mice Model and Its Modulatory Impact on Gut Microbiota Metabolism.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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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.
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.
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Who cites it
3 citing papers in PubMed.
- Intermittent Fasting and the Gut Microbiota: Mechanisms Linking Microbial Remodeling to Metabolic and Immune Regulation.Nutrients · 2026Review
- Time vortex: the circadian-dopaminergic dialogue in Parkinson's disease.NPJ Parkinson's disease · 2026Review
- Dietary Yam (Nutrients · 2026Article
Corrections and comments
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Authors and funding
13 authors.
Funding
Abstract
Dietary interventions alleviate Parkinson's disease (PD) progression by modulating the gut microbiota. However, the interaction between time-restricted feeding (TRF) and dietary protein composition remains unclear. This study examines the effects of casein (animal-derived) and soy protein (plant-derived) on PD pathology in an MPTP-induced mouse model and their influence on TRF efficacy. MPTP induces dopaminergic neuron loss and neuroinflammation regardless of protein source, but casein-fed mice show partial motor dysfunction and gut barrier disruption, whereas soy protein-fed mice maintain motor function and barrier integrity. TRF differentially modulates PD outcomes: in casein-fed mice, it alleviates partial motor deficits by suppressing monoamine oxidase B (MAO-B) and reducing dopamine (DA) metabolism, without rescuing DA levels or neuron survival. In soy protein-fed mice, TRF suppresses MAO-B, preserves dopaminergic neurons, restores DA levels, and reduces neuroinflammation. Analysis of gut microbiota and metabolomics suggests that TRF may reduce Allobaculum and branched-chain amino acids (BCAAs) in casein-fed mice, while increasing Akkermansia and short-chain fatty acids (SCFAs) in soy protein-fed mice. Mechanistic assays suggest that Allobaculum and BCAAs impair gut barrier function and aggravate inflammation. In conclusion, TRF exerts protein-dependent neuroprotective effects, with soy protein combined with TRF offering a promising dietary strategy for PD management.
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Registered trials
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