Probiotics Affect One-Carbon Metabolites and Catecholamines in a Genetic Rat Model of Depression

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SCOPE: Probiotics may influence one-carbon (C1) metabolism, neurotransmitters, liver function markers, or behavior.

METHODS AND RESULTS: Male adult Flinders Sensitive Line rats (model of depression, FSL; n = 22) received Lactobacillus helveticus R0052 and Bifidobacterium longum R0175 (109or 1010colony-forming units/d) or vehicle for 10 weeks. The controls, Flinders Resistant Line rats (FRL, n = 8), only received vehicle. C1-related metabolites were measured in plasma, urine, and different tissues. Monoamine concentrations were measured in plasma, hippocampus, and prefrontal cortex. Vehicle-treated FSL rats had higher plasma concentrations of betaine, choline, and dimethylglycine, but lower plasma homocysteine and liver S-adenosylmethionine (SAM) than FRLs. FSL rats receiving high-dose probiotics had lower plasma betaine and higher liver SAM compared to vehicle-treated FSL rats. FSLs had higher concentrations of norepinephrine, dopamine, and serotonin than FRLs across various brain regions. Probiotics decreased plasma dopamine in FSLs in a dose-dependent manner. There were no detectable changes in liver function markers or behavior.

CONCLUSIONS: Probiotics reduced the flow of methyl groups via betaine, increased liver SAM, and decreased plasma dopamine and norepinephrine. Since these changes in methylation and catecholamine pathways are known to be involved in several diseases, future investigation of the effect of probiotics is warranted. This article is protected by copyright. All rights reserved.

Original languageEnglish
Article number1701070
JournalMolecular Nutrition & Food Research
Volume62
Issue7
Pages (from-to)e1701070
Number of pages10
ISSN1613-4125
Publication statusPublished - 2018

    Research areas

  • depression, dopamine, gut–brain axis, probiotics, S-adenosylmethionine, Lactobacillus helveticus/growth & development, Probiotics/administration & dosage, Dopamine/blood, Prefrontal Cortex/metabolism, Male, Behavior, Animal, Dopamine Antagonists/administration & dosage, Norepinephrine/antagonists & inhibitors, S-Adenosylmethionine/antagonists & inhibitors, Rats, Mutant Strains, Liver/metabolism, Antidepressive Agents/administration & dosage, Biomarkers/blood, Depression/blood, Freeze Drying, Homocysteine/antagonists & inhibitors, Random Allocation, Animals, Neurons/metabolism, Bifidobacterium longum/growth & development, Hippocampus/metabolism, Methylation

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