Probiotic Lactobacillus plantarum 299v supplementation in patients with major depression in a double-blind, randomized, placebo-controlled trial: A metabolomics study.

Chiral amino acids analysis LP299v MDD Major depression Probiotic supplementation Untargeted metabolomics

Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
11 Sep 2024
Historique:
received: 10 03 2024
revised: 19 06 2024
accepted: 10 09 2024
medline: 14 9 2024
pubmed: 14 9 2024
entrez: 13 9 2024
Statut: aheadofprint

Résumé

Understanding the multifactorial nature of major depressive disorder (MDD) is crucial for tailoring treatments. However, the complex interplay of various factors underlying the development and progression of MDD poses significant challenges. Our previous study demonstrated improvements in cognitive functions in MDD patients undergoing treatment with selective serotonin reuptake inhibitors (SSRIs) supplemented with Lactobacillus plantarum 299v (LP299v). To elucidate the biochemical mechanisms underlying cognitive functions improvements, we explored underlying metabolic changes. We employed multi-platform metabolomics, including LC-QTOF-MS and CE-TOF-MS profiling, alongside chiral LC-QqQ-MS analysis for amino acids. Supplementation of SSRI treatment with LP299v intensified the reduction of long-chain acylcarnitines, potentially indicating improved mitochondrial function. LP299v supplementation reduced N-acyl taurines more than four times compared to the placebo, suggesting a substantial impact on restoring biochemical balance. The LP299v-supplemented group showed increased levels of oxidized glycerophosphocholine (oxPC). Additionally, LP299v supplementation led to higher levels of sphingomyelins, L-histidine, D-valine, and p-cresol. This exploratory study suggests potential metabolic pathways influenced by LP299v supplementation. However, the need for further research hinders the ability to draw definitive conclusions. Observed metabolic alterations were linked to mitochondrial dysfunction, inflammation, oxidative stress and gut microbiota alterations. Despite the subtle nature of their alterations, our research successfully detected these differences and connected them to the metabolic disruptions associated with MDD. Our findings emphasise the intricate relationship between metabolism, gut microbiota, and mental health prompting further research into the mechanisms of action of probiotics in MDD treatment.

Sections du résumé

BACKGROUND BACKGROUND
Understanding the multifactorial nature of major depressive disorder (MDD) is crucial for tailoring treatments. However, the complex interplay of various factors underlying the development and progression of MDD poses significant challenges. Our previous study demonstrated improvements in cognitive functions in MDD patients undergoing treatment with selective serotonin reuptake inhibitors (SSRIs) supplemented with Lactobacillus plantarum 299v (LP299v).
METHODS METHODS
To elucidate the biochemical mechanisms underlying cognitive functions improvements, we explored underlying metabolic changes. We employed multi-platform metabolomics, including LC-QTOF-MS and CE-TOF-MS profiling, alongside chiral LC-QqQ-MS analysis for amino acids.
RESULTS RESULTS
Supplementation of SSRI treatment with LP299v intensified the reduction of long-chain acylcarnitines, potentially indicating improved mitochondrial function. LP299v supplementation reduced N-acyl taurines more than four times compared to the placebo, suggesting a substantial impact on restoring biochemical balance. The LP299v-supplemented group showed increased levels of oxidized glycerophosphocholine (oxPC). Additionally, LP299v supplementation led to higher levels of sphingomyelins, L-histidine, D-valine, and p-cresol.
LIMITATIONS CONCLUSIONS
This exploratory study suggests potential metabolic pathways influenced by LP299v supplementation. However, the need for further research hinders the ability to draw definitive conclusions.
CONCLUSIONS CONCLUSIONS
Observed metabolic alterations were linked to mitochondrial dysfunction, inflammation, oxidative stress and gut microbiota alterations. Despite the subtle nature of their alterations, our research successfully detected these differences and connected them to the metabolic disruptions associated with MDD. Our findings emphasise the intricate relationship between metabolism, gut microbiota, and mental health prompting further research into the mechanisms of action of probiotics in MDD treatment.

Identifiants

pubmed: 39271063
pii: S0165-0327(24)01543-X
doi: 10.1016/j.jad.2024.09.058
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest.

Auteurs

Joanna Godzien (J)

Metabolomics Laboratory, Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Bartlomiej Kalaska (B)

Department of Pharmacodynamics, Medical University of Bialystok, Bialystok, Poland. Electronic address: bartlomiej.kalaska@umb.edu.pl.

Leszek Rudzki (L)

Psychiatry-UK, 3b Fore Street, Camelford PL32 9PG, UK.

Cecilia Barbas Bernardos (CB)

Centro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain.

Justyna Swieton (J)

Department of Pharmacodynamics, Medical University of Bialystok, Bialystok, Poland.

Angeles Lopez-Gonzalvez (A)

Centro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain.

Lucyna Ostrowska (L)

Department of Dietetics and Clinical Nutrition, Medical University of Bialystok, Bialystok, Poland.

Agata Szulc (A)

Department of Psychiatry, Medical University of Warsaw, Warsaw, Poland.

Napoleon Waszkiewicz (N)

Department of Psychiatry, Medical University of Bialystok, Bialystok, Poland.

Michal Ciborowski (M)

Metabolomics Laboratory, Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Antonia García (A)

Centro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain.

Adam Kretowski (A)

Metabolomics Laboratory, Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Coral Barbas (C)

Centro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain.

Dariusz Pawlak (D)

Department of Pharmacodynamics, Medical University of Bialystok, Bialystok, Poland.

Classifications MeSH