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Butyrate Rescues Oxidative Stress-Induced Transport Deficits of Tryptophan: Potential Implication in Affective or
Julia Rode1, Lin Yang2, Julia König1
1Nutrition-Gut-Brain Interactions Research Centre, School of Medical Sciences, Örebro University, Örebro, Sweden.
Neuropsychobiology
|October 19, 2020
Summary
Butyrate, a gut microbiota metabolite, counteracts oxidative stress that impairs tryptophan transport. This finding suggests butyrate
Area of Science:
- Neuroscience
- Microbiology
- Biochemistry
Background:
- Butyrate, a short-chain fatty acid produced by gut microbiota, exhibits antioxidant properties.
- Butyrate influences neurological functions and is implicated in gut-brain interactions relevant to affective disorders.
Purpose of the Study:
- To investigate how oxidative stress affects tryptophan transport, a key factor in affective disorders.
- To determine if butyrate can mitigate these negative effects due to its antioxidant capacity and influence on tryptophan transport.
Main Methods:
- Human skin fibroblasts were exposed to hydrogen peroxide to induce oxidative stress.
- Cells were treated with varying concentrations of butyrate.
- Tryptophan uptake was measured using a radiotracer, and gene expression of amino acid transporters was analyzed.
Main Results:
- Oxidative stress significantly reduced tryptophan uptake in fibroblasts.
- Butyrate treatment reversed the decrease in tryptophan uptake caused by oxidative stress.
- Butyrate differentially regulated the gene expression of large amino acid transporters 1 and 2 in stressed and control cells.
Conclusions:
- Gut microbiota-derived butyrate shows therapeutic potential for affective disorders.
- Butyrate may counteract oxidative stress-induced disruptions in tryptophan transport, potentially benefiting conditions with altered serotonergic activity or neuroinflammation.
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