Literature DB >> 26423130

The gut-brain axis: interactions between Helicobacter pylori and enteric and central nervous systems.

Jannis Kountouras1, Christos Zavos1, Stergios A Polyzos1, Georgia Deretzi2.   

Abstract

Entities:  

Year:  2015        PMID: 26423130      PMCID: PMC4585404     

Source DB:  PubMed          Journal:  Ann Gastroenterol        ISSN: 1108-7471


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Carabotti et al [1] suggested that gut microbiota has an important role in bidirectional interactions between the gut and the central nervous system (CNS). In this regard, we considered gastrointestinal immune system and brain dialogue, particularly implicated in neuroinflammation, as a common feature of the neurodegenerative and neuroinflammatory diseases [2]. Neuroinflammation might initiate from gastrointestinal track (GIT), a vulnerable area through which pathogens influence the brain. A proposed mechanism from GIT (i.e., “little brain”) infections including Helicobacter pylori (Hp) current infection to the CNS (i.e., “big brain”) neuroinflammation, is that the pathogen may access the brain through the blood, the oral-nasal olfactory and the faster GIT-associated retrograde axonal transport pathways [2,3]. Specifically, Hp induces relative mechanisms and/or mediators such as the synthesis of various cytokines and/or chemokines, which may be detrimental to the CNS inflammation and/or neurodegeneration. Hp, by inducing several inflammatory mediators such as tumor necrosis factor-α and interleukin (IL)-6, may contribute to blood-brain barrier (ΒΒΒ) disruption leading to brain neurodegenerative diseases. In addition, Hp-induced vacuolating A cytotoxin exhibits chemotactic activities to the bone marrow-derived mast cells (BMD-MCs) and induces BMD-MCs to produce proinflammatory cytokines leading to BBB dysfunction; MCs can be stimulated by corticotropin releasing hormone, also mentioned by the authors [1], including histamine, IL-8, tryptase and vascular endothelial growth factor which disrupt the BBB. Likewise, human defensins might contribute to Hp-related brain pathologies by modulating innate and adaptive immune system responses. Finally, activated monocytes (possibly infected with Hp due to defective autophagy resulting in Hp replication in autophagic vesicles) might also access the brain due to BBB disruption (Trojan horse theory) contributing to Hp-related neurodegeneration [2-5]. Importantly, Hippocrates wisely remarked: “all the diseases begin in the gut” and “death sits in the bowel”, thereby creating the hypothesis that gut is responsible for many disorders including neurodegenerative diseases.
  5 in total

1.  Helicobacter pylori and multiple sclerosis.

Authors:  Emmanuel Gavalas; Jannis Kountouras; Georgia Deretzi; Marina Boziki; Nikolaos Grigoriadis; Christos Zavos; Ioannis Venizelos
Journal:  J Neuroimmunol       Date:  2007-07-05       Impact factor: 3.478

2.  From the "little brain" gastrointestinal infection to the "big brain" neuroinflammation: a proposed fast axonal transport pathway involved in multiple sclerosis.

Authors:  Georgia Deretzi; Jannis Kountouras; Nikolaos Grigoriadis; Christos Zavos; Stavros Chatzigeorgiou; Evangelos Koutlas; Iakovos Tsiptsios
Journal:  Med Hypotheses       Date:  2009-05-24       Impact factor: 1.538

3.  Relationship between Helicobacter pylori infection and Alzheimer disease.

Authors:  J Kountouras; M Tsolaki; E Gavalas; M Boziki; C Zavos; P Karatzoglou; D Chatzopoulos; I Venizelos
Journal:  Neurology       Date:  2006-03-28       Impact factor: 9.910

Review 4.  Gastrointestinal immune system and brain dialogue implicated in neuroinflammatory and neurodegenerative diseases.

Authors:  G Deretzi; J Kountouras; S A Polyzos; C Zavos; E Giartza-Taxidou; E Gavalas; I Tsiptsios
Journal:  Curr Mol Med       Date:  2011-11       Impact factor: 2.222

5.  The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems.

Authors:  Marilia Carabotti; Annunziata Scirocco; Maria Antonietta Maselli; Carola Severi
Journal:  Ann Gastroenterol       Date:  2015 Apr-Jun
  5 in total
  6 in total

1.  Potential impact of Helicobacter pylori-related human β-defensin-1 on hepatic encephalopathy and neurodegeneration.

Authors:  Jannis Kountouras; Christos Zavos; Stergios A Polyzos; Georgia Deretzi
Journal:  Ann Gastroenterol       Date:  2016 Jan-Mar

2.  The role of stomach in neurological disorders: 1000 years historical background.

Authors:  Arman Zargaran; Hossein Rezaeizadeh
Journal:  Ann Gastroenterol       Date:  2016 Jan-Mar

3.  Helicobacter pylori infection and low dietary iron alter behavior, induce iron deficiency anemia, and modulate hippocampal gene expression in female C57BL/6 mice.

Authors:  Monika Burns; Aldo Amaya; Caroline Bodi; Zhongming Ge; Vasudevan Bakthavatchalu; Kathleen Ennis; Timothy C Wang; Michael Georgieff; James G Fox
Journal:  PLoS One       Date:  2017-03-29       Impact factor: 3.240

Review 4.  Helicobacter pylori infection: Beyond gastric manifestations.

Authors:  Maria Luísa Cordeiro Santos; Breno Bittencourt de Brito; Filipe Antônio França da Silva; Mariana Miranda Sampaio; Hanna Santos Marques; Natália Oliveira E Silva; Dulciene Maria de Magalhães Queiroz; Fabrício Freire de Melo
Journal:  World J Gastroenterol       Date:  2020-07-28       Impact factor: 5.742

Review 5.  Helicobacter pylori and unignorable extragastric diseases: Mechanism and implications.

Authors:  Junjian He; Yunyi Liu; Qin Ouyang; Rongxing Li; Jie Li; Weiyan Chen; Weichao Hu; Lijiao He; Qiyu Bao; Ping Li; Changjiang Hu
Journal:  Front Microbiol       Date:  2022-08-04       Impact factor: 6.064

6.  Electroacupuncture Upregulated Ghrelin in Rats with Functional Dyspepsia via AMPK/TSC2/Rheb-Mediated mTOR Inhibition.

Authors:  Lei Tang; Yi Zeng; Lei Li; Jingjing Wang; Duo Peng; Ting Zhang; Hongxing Zhang; Xue An
Journal:  Dig Dis Sci       Date:  2019-12-21       Impact factor: 3.199

  6 in total

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