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Review
. 2015 May 1;37(5):984-95.
doi: 10.1016/j.clinthera.2015.04.002.

Gut-Microbiota-Brain Axis and Its Effect on Neuropsychiatric Disorders With Suspected Immune Dysregulation

Affiliations
Review

Gut-Microbiota-Brain Axis and Its Effect on Neuropsychiatric Disorders With Suspected Immune Dysregulation

Anastasia I Petra et al. Clin Ther. .

Abstract

Purpose: Gut microbiota regulate intestinal function and health. However, mounting evidence indicates that they can also influence the immune and nervous systems and vice versa. This article reviews the bidirectional relationship between the gut microbiota and the brain, termed the microbiota-gut-brain (MGB) axis, and discusses how it contributes to the pathogenesis of certain disorders that may involve brain inflammation.

Methods: Articles were identified with a search of Medline (starting in 1980) by using the key words anxiety, attention-deficit hypersensitivity disorder (ADHD), autism, cytokines, depression, gut, hypothalamic-pituitary-adrenal (HPA) axis, inflammation, immune system, microbiota, nervous system, neurologic, neurotransmitters, neuroimmune conditions, psychiatric, and stress.

Findings: Various afferent or efferent pathways are involved in the MGB axis. Antibiotics, environmental and infectious agents, intestinal neurotransmitters/neuromodulators, sensory vagal fibers, cytokines, and essential metabolites all convey information to the central nervous system about the intestinal state. Conversely, the hypothalamic-pituitary-adrenal axis, the central nervous system regulatory areas of satiety, and neuropeptides released from sensory nerve fibers affect the gut microbiota composition directly or through nutrient availability. Such interactions seem to influence the pathogenesis of a number of disorders in which inflammation is implicated, such as mood disorder, autism-spectrum disorders, attention-deficit hypersensitivity disorder, multiple sclerosis, and obesity.

Implications: Recognition of the relationship between the MGB axis and the neuroimmune systems provides a novel approach for better understanding and management of these disorders. Appropriate preventive measures early in life or corrective measures such as use of psychobiotics, fecal microbiota transplantation, and flavonoids are discussed.

Keywords: MGB axis; cytokines; gut; immune disorders; microbiota; nervous system diseases.

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Conflict of interest statement

Conflicts of interests

The authors declare no conflicts.

Figures

Figure 1
Figure 1. Diagrammatic representation of the M-G-B axis showing the proposed bidirectional communications
Gut microbiota can release molecules that can: activate the neuroenteric plexus, stimulate brain production of neuropeptides, as well as increase gut-blood barrier and BBB permeability. The brain releases molecules that stimulate the neuroenteric plexus and gut function. The vagus nerve sends orthodromic and antidromic. Ach= Acetylcholine BBB= Blood-brain barrier CRH= Corticotropin-releasing hormone 5-HT= 5-hydroxytryptamine IL-6= Interleukin 6 NT= Neurotensin SP= Substance P TNF= Tumor necrosis factor VIP= Vasoactive intestinal peptide

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