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Potential neuro-immune therapeutic targets in irritable bowel syndrome.

作者信息

Casado-Bedmar Maite, Keita Åsa V

机构信息

Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.

Department of Biomedical and Clinical Sciences, Medical Faculty, Linköping University, Campus US, Linköping, 581 85, Sweden.

出版信息

Therap Adv Gastroenterol. 2020 Apr 9;13:1756284820910630. doi: 10.1177/1756284820910630. eCollection 2020.


DOI:10.1177/1756284820910630
PMID:32313554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7153177/
Abstract

Irritable bowel syndrome (IBS) is a functional gastrointestinal (GI) disorder characterized by recurring abdominal pain and disturbed bowel habits. The aetiology of IBS is unknown but there is evidence that genetic, environmental and immunological factors together contribute to the development of the disease. Current treatment of IBS includes lifestyle and dietary interventions, laxatives or antimotility drugs, probiotics, antispasmodics and antidepressant medication. The gut-brain axis comprises the central nervous system, the hypothalamic pituitary axis, the autonomic nervous system and the enteric nervous system. Within the intestinal mucosa there are close connections between immune cells and nerve fibres of the enteric nervous system, and signalling between, for example, mast cells and nerves has shown to be of great importance during GI disorders such as IBS. Communication between the gut and the brain is most importantly routed the vagus nerve, where signals are transmitted by neuropeptides. It is evident that IBS is a disease of a gut-brain axis dysregulation, involving altered signalling between immune cells and neurotransmitters. In this review, we analyse the most novel and distinct neuro-immune interactions within the IBS mucosa in association with already existing and potential therapeutic targets.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47ad/7153177/5a57f7a2c0f5/10.1177_1756284820910630-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47ad/7153177/5a57f7a2c0f5/10.1177_1756284820910630-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47ad/7153177/5a57f7a2c0f5/10.1177_1756284820910630-fig1.jpg

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[2]
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[4]
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[5]
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[6]
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[7]
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World J Gastroenterol. 2022-3-28

[8]
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World J Gastroenterol. 2022-1-28

[9]
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[10]
Intestinal Homeostasis under Stress Siege.

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本文引用的文献

[1]
Increased Colonic Epithelial Permeability and Mucosal Eosinophilia in Ulcerative Colitis in Remission Compared With Irritable Bowel Syndrome and Health.

Inflamm Bowel Dis. 2020-6-18

[2]
In major depression, increased kappa and mu opioid receptor levels are associated with immune activation.

Acta Neuropsychiatr. 2020-1-14

[3]
Endogenous control of inflammatory visceral pain by T cell-derived opioids in IL-10-deficient mice.

Neurogastroenterol Motil. 2020-2

[4]
Miltefosine treatment reduces visceral hypersensitivity in a rat model for irritable bowel syndrome via multiple mechanisms.

Sci Rep. 2019-8-29

[5]
Berberine prevents stress-induced gut inflammation and visceral hypersensitivity and reduces intestinal motility in rats.

World J Gastroenterol. 2019-8-7

[6]
µ-opioid receptor, β-endorphin, and cannabinoid receptor-2 are increased in the colonic mucosa of irritable bowel syndrome patients.

Neurogastroenterol Motil. 2019-7-23

[7]
Effectiveness of mesalazine to treat irritable bowel syndrome: A meta-analysis.

Medicine (Baltimore). 2019-7

[8]
New insights into the interplay between autophagy, gut microbiota and inflammatory responses in IBD.

Autophagy. 2019-7-9

[9]
Berberine ameliorates diabetic neuropathic pain in a rat model: involvement of oxidative stress, inflammation, and μ-opioid receptors.

Naunyn Schmiedebergs Arch Pharmacol. 2019-5-12

[10]
The place of tachykinin NK2 receptor antagonists in the treatment diarrhea-predominant irritable bowel syndrome.

J Physiol Pharmacol. 2019-4-20

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