Alterations in Vagal Tone Are Associated with Changes in the Gut Microbiota of Adults with Anxiety and Depression Symptoms: Analysis of Fecal Metabolite Profiles

被引:0
作者
Pasqualette, Laura [1 ,2 ]
Fidalgo, Tatiana Kelly da Silva [3 ]
Freitas-Fernandes, Liana Bastos [4 ]
Souza, Gabriela Guerra Leal [5 ]
Imbiriba, Luis Aureliano [6 ]
Lobo, Leandro Araujo [1 ]
Volchan, Eliane [7 ]
Domingues, Regina Maria Cavalcanti Pilotto [1 ]
Valente, Ana Paula [4 ]
Miranda, Karla Rodrigues [1 ]
机构
[1] Univ Fed Rio De Janeiro, Inst Microbiol Paulo Goes, BR-21941902 Rio De Janeiro, Brazil
[2] Univ Bremen, Dev & Educ Psychol, D-28359 Bremen, Germany
[3] Univ Estado Rio De Janeiro, Dept Prevent & Community Dent, Pediat Dent, BR-20551030 Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Natl Ctr Nucl Magnet Resonance CENABIO, Med Biochem, BR-21941902 Rio De Janeiro, Brazil
[5] Univ Fed Ouro Preto, Dept Biol Sci, Lab Psychophysiol, BR-35400000 Ouro Preto, Brazil
[6] Univ Fed Rio de Janeiro, Sch Phys Educ & Sports, BR-21941599 Rio De Janeiro, Brazil
[7] Univ Fed Rio de Janeiro, Inst Biophys Carlos Chagas Filho, BR-21941902 Rio De Janeiro, Brazil
关键词
metabolomics; gut-brain axis; depression; anxiety; vagal tone; gut microbiota; amino acids; short-chain fatty acids; HEART-RATE-VARIABILITY; STRESS; BUTYRATE; ANTIDEPRESSANT; METABOLOMICS; INFLAMMATION; EXPRESSION; INVENTORY; ASPARTATE; BEHAVIOR;
D O I
10.3390/metabo14080450
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulating evidence suggests that interactions between the brain and gut microbiota significantly impact brain function and mental health. In the present study, we aimed to investigate whether young, healthy adults without psychiatric diagnoses exhibit differences in metabolic stool and microbiota profiles based on depression/anxiety scores and heart rate variability (HRV) parameters. Untargeted nuclear magnetic resonance-based metabolomics was used to identify fecal metabolic profiles. Results were subjected to multivariate analysis through principal component analysis (PCA) and partial least squares discriminant analysis (PLS-DA), and the metabolites were identified through VIP score. Metabolites separating asymptomatic and symptomatic groups were acetate, valine, and glutamate, followed by sugar regions, glutamine, acetone, valerate, and acetoacetate. The main metabolites identified in high vagal tone (HVT) and low vagal tone (LVT) groups were acetate, valerate, and glutamate, followed by propionate and butyrate. In addition to the metabolites identified by the PLS-DA test, significant differences in aspartate, sarcosine, malate, and methionine were observed between the groups. Levels of acetoacetate were higher in both symptomatic and LVT groups. Valerate levels were significantly increased in the symptomatic group, while isovalerate, propionate, glutamate, and acetone levels were significantly increased in the LVT group. Furthermore, distinct abundance between groups was only confirmed for the Firmicutes phylum. Differences between participants with high and low vagal tone suggest that certain metabolites are involved in communication between the vagus nerve and the brain.
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页数:16
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共 88 条
[1]   Enzymes involved in branched-chain amino acid metabolism in humans [J].
Adeva-Andany, Maria M. ;
Lopez-Maside, Laura ;
Donapetry-Garcia, Cristobal ;
Fernandez-Fernandez, Carlos ;
Sixto-Leal, Cristina .
AMINO ACIDS, 2017, 49 (06) :1005-1028
[2]   The tryptophan catabolite or kynurenine pathway in major depressive and bipolar disorder: A systematic review and meta-analysis [J].
Almulla, Abbas F. ;
Thipakorn, Yanin ;
Vasupanrajit, Asara ;
Algon, Ali Abbas Abo ;
Tunvirachaisakul, Chavit ;
Aljanabi, Ashwan Abdulzahra Hashim ;
Oxenkrug, Gregory ;
Al-Hakeim, Hussein K. ;
Maes, Michael .
BRAIN BEHAVIOR & IMMUNITY-HEALTH, 2022, 26
[3]  
American Psychological Society, 2013, Diagnostic and statistical manual of mental disorders, V5th ed.
[5]   Exogenous Ketone Supplements Reduce Anxiety-Related Behavior in Sprague-Dawley and Wistar Albino Glaxo/Rijs']jswijk Rats (vol 9, 137, 2016) [J].
Ari, Csilla ;
Kovacs, Zsolt ;
Juhasz, Gabor ;
Murdun, Cem ;
Goldhagen, Craig R. ;
Koutnik, Andrew P. ;
Poff, Angela M. ;
Kesl, Shannon L. ;
D'Agostino, Dominic P. .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2017, 10
[6]   Gut Microbiota-Derived Inflammation-Related Serum Metabolites as Potential Biomarkers for Major Depressive Disorder [J].
Bai, Shunjie ;
Xie, Jing ;
Bai, Huili ;
Tian, Tian ;
Zou, Tao ;
Chen, Jian-Jun .
JOURNAL OF INFLAMMATION RESEARCH, 2021, 14 :3755-3766
[7]   Branched-Chain Amino Acids as New Biomarkers of Major Depression - A Novel Neurobiology of Mood Disorder [J].
Baranyi, Andreas ;
Amouzadeh-Ghadikolai, Omid ;
von Lewinski, Dirk ;
Rothenhaeusler, Hans-Bernd ;
Theokas, Simon ;
Robier, Christoph ;
Mangge, Harald ;
Reicht, Gerhard ;
Hlade, Peter ;
Meinitzer, Andreas .
PLOS ONE, 2016, 11 (08)
[8]   AN INVENTORY FOR MEASURING DEPRESSION [J].
BECK, AT ;
ERBAUGH, J ;
WARD, CH ;
MOCK, J ;
MENDELSOHN, M .
ARCHIVES OF GENERAL PSYCHIATRY, 1961, 4 (06) :561-&
[9]   Gut Microbiota Dysbiosis Associated With Altered Production of Short Chain Fatty Acids in Children With Neurodevelopmental Disorders [J].
Bojovic, Katarina ;
Ignjatovic, Durdica ;
Bajic, Svetlana Sokovic ;
Milutinovic, Danijela Vojnovic ;
Tomic, Mirko ;
Golic, Natasa ;
Tolinacki, Maja .
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2020, 10
[10]   The gut microbiota influences blood-brain barrier permeability in mice [J].
Braniste, Viorica ;
Al-Asmakh, Maha ;
Kowal, Czeslawa ;
Anuar, Farhana ;
Abbaspour, Afrouz ;
Toth, Miklos ;
Korecka, Agata ;
Bakocevic, Nadja ;
Ng, Lai Guan ;
Kundu, Parag ;
Gulyas, Balazs ;
Halldin, Christer ;
Hultenby, Kjell ;
Nilsson, Harriet ;
Hebert, Hans ;
Volpe, Bruce T. ;
Diamond, Betty ;
Pettersson, Sven .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (263)