» Articles » PMID: 27965654

The Neuro-endocrinological Role of Microbial Glutamate and GABA Signaling

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2016 Dec 15
PMID 27965654
Citations 150
Authors
Affiliations
Soon will be listed here.
Abstract

Gut microbiota provides the host with multiple functions (e.g., by contributing to food digestion, vitamin supplementation, and defense against pathogenic strains) and interacts with the host organism through both direct contact (e.g., through surface antigens) and soluble molecules, which are produced by the microbial metabolism. The existence of the so-called gut-brain axis of bi-directional communication between the gastrointestinal tract and the central nervous system (CNS) also supports a communication pathway between the gut microbiota and neural circuits of the host, including the CNS. An increasing body of evidence has shown that gut microbiota is able to modulate gut and brain functions, including the mood, cognitive functions, and behavior of humans. Nonetheless, given the extreme complexity of this communication network, its comprehension is still at its early stage. The present contribution will attempt to provide a state-of-the art description of the mechanisms by which gut microbiota can affect the gut-brain axis and the multiple cellular and molecular communication circuits (i.e., neural, immune, and humoral). In this context, special attention will be paid to the microbial strains that produce bioactive compounds and display ascertained or potential probiotic activity. Several neuroactive molecules (e.g., catecholamines, histamine, serotonin, and trace amines) will be considered, with special focus on Glu and GABA circuits, receptors, and signaling. From the basic science viewpoint, "microbial endocrinology" deals with those theories in which neurochemicals, produced by both multicellular organisms and prokaryotes (e.g., serotonin, GABA, glutamate), are considered as a common shared language that enables interkingdom communication. With regards to its application, research in this area opens the way toward the possibility of the future use of neuroactive molecule-producing probiotics as therapeutic agents for the treatment of neurogastroenteric and/or psychiatric disorders.

Citing Articles

Psycho-gastroenterological profile of an Italian population of children with disorders of gut-brain interaction: A case-control study.

Giorgio V, Venezia I, Pensabene L, Blasi E, Rigante D, Mariotti P World J Clin Pediatr. 2025; 14(1):97543.

PMID: 40059898 PMC: 11686583. DOI: 10.5409/wjcp.v14.i1.97543.


Exploring Gut Microbiota-Targeted Therapies for Canine Idiopathic Epilepsy.

Blanquet L, Serra D, Marrinhas C, Almeida A Int J Mol Sci. 2025; 26(4).

PMID: 40004205 PMC: 11855791. DOI: 10.3390/ijms26041742.


Anxiety disorders and the gut microbiota: a bibliometric and visual analysis.

Guo L, Ding Q, Li Q, Zheng D, Guo L, Cao X Front Psychiatry. 2025; 15:1517508.

PMID: 39902242 PMC: 11788897. DOI: 10.3389/fpsyt.2024.1517508.


Metabolics-Based Study on the Therapeutic Mechanism Behind the Effect of Shenhuang Plaster Applied to the Shenque Acupoint on Gastrointestinal Motility in POI Mice.

Shi Y, Wu C, Liu T, Wang R, Ding B, Sun Q Metabolites. 2025; 15(1).

PMID: 39852407 PMC: 11767606. DOI: 10.3390/metabo15010065.


Exploring Gut Microbiota Imbalance in Irritable Bowel Syndrome: Potential Therapeutic Effects of Probiotics and Their Metabolites.

Garcia Mansilla M, Rodriguez Sojo M, Lista A, Ayala Mosqueda C, Ruiz Malagon A, Galvez J Nutrients. 2025; 17(1.

PMID: 39796588 PMC: 11723002. DOI: 10.3390/nu17010155.


References
1.
Keita A, Soderholm J . The intestinal barrier and its regulation by neuroimmune factors. Neurogastroenterol Motil. 2010; 22(7):718-33. DOI: 10.1111/j.1365-2982.2010.01498.x. View

2.
Buka S, Cannon T, Torrey E, Yolken R . Maternal exposure to herpes simplex virus and risk of psychosis among adult offspring. Biol Psychiatry. 2007; 63(8):809-15. DOI: 10.1016/j.biopsych.2007.09.022. View

3.
Berntson G, Sarter M, Cacioppo J . Ascending visceral regulation of cortical affective information processing. Eur J Neurosci. 2003; 18(8):2103-9. DOI: 10.1046/j.1460-9568.2003.02967.x. View

4.
Gadea A, Lopez-Colome A . Glial transporters for glutamate, glycine, and GABA: II. GABA transporters. J Neurosci Res. 2001; 63(6):461-8. DOI: 10.1002/jnr.1040. View

5.
Zareian M, Ebrahimpour A, Abu Bakar F, Mohamed A, Forghani B, Ab-Kadir M . A glutamic acid-producing lactic acid bacteria isolated from Malaysian fermented foods. Int J Mol Sci. 2012; 13(5):5482-5497. PMC: 3382744. DOI: 10.3390/ijms13055482. View