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肥大细胞调节:肠易激综合征腹痛的一种新的治疗策略。

Mast cell modulation: A novel therapeutic strategy for abdominal pain in irritable bowel syndrome.

机构信息

Translational Research Centre for Gastrointestinal Disorders, KU Leuven, Leuven, Belgium.

Translational Research Centre for Gastrointestinal Disorders, KU Leuven, Leuven, Belgium.

出版信息

Cell Rep Med. 2024 Oct 15;5(10):101780. doi: 10.1016/j.xcrm.2024.101780. Epub 2024 Oct 7.


DOI:10.1016/j.xcrm.2024.101780
PMID:39378882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11513802/
Abstract

Irritable bowel syndrome (IBS) is one of the most prevalent gastrointestinal disorders characterized by recurrent abdominal pain and an altered defecation pattern. Chronic abdominal pain represents the hallmark IBS symptom and is reported to have the most bothersome impact on the patient's quality of life. Unfortunately, effective therapeutic strategies reducing abdominal pain are lacking, mainly attributed to a limited understanding of the contributing mechanisms. In the past few years, exciting new insights have pointed out that altered communication between gut immune cells and pain-sensing nerves acts as a hallmark driver of IBS-related abdominal pain. In this review, we aim to summarize our current knowledge on altered neuro-immune crosstalk as the main driver of altered pain signaling, with a specific focus on altered mast cell functioning herein, and highlight the relevance of targeting mast cell-mediated mechanisms as a novel therapeutic strategy for chronic abdominal pain in IBS patients.

摘要

肠易激综合征(IBS)是最常见的胃肠道疾病之一,其特征为反复腹痛和排便习惯改变。慢性腹痛是 IBS 的标志性症状,据报道对患者的生活质量有最严重的影响。不幸的是,目前缺乏能够减轻腹痛的有效治疗策略,这主要归因于对发病机制的了解有限。在过去的几年中,令人兴奋的新见解指出,肠道免疫细胞和痛觉神经之间的通讯改变是导致 IBS 相关腹痛的主要驱动因素。在这篇综述中,我们旨在总结目前关于神经免疫串扰改变作为疼痛信号改变的主要驱动因素的知识,特别关注其中改变的肥大细胞功能,并强调靶向肥大细胞介导的机制作为 IBS 患者慢性腹痛的一种新的治疗策略的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/bf83b84fc4de/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/62c60dfa2fc6/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/ecb4717fa9a4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/9591ba4d39a5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/744682c36cca/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/bf83b84fc4de/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/62c60dfa2fc6/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/ecb4717fa9a4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/9591ba4d39a5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/744682c36cca/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/11513802/bf83b84fc4de/gr4.jpg

相似文献

[1]
Mast cell modulation: A novel therapeutic strategy for abdominal pain in irritable bowel syndrome.

Cell Rep Med. 2024-10-15

[2]
Irritable bowel syndrome: When food is a pain in the gut.

Immunol Rev. 2024-9

[3]
Immune activation in irritable bowel syndrome: what is the evidence?

Nat Rev Immunol. 2022-11

[4]
Local immune response as novel disease mechanism underlying abdominal pain in patients with irritable bowel syndrome.

Acta Clin Belg. 2022-10

[5]
Intestinal serotonin release, sensory neuron activation, and abdominal pain in irritable bowel syndrome.

Am J Gastroenterol. 2011-3-22

[6]
Activated mast cells in proximity to colonic nerves correlate with abdominal pain in irritable bowel syndrome.

Gastroenterology. 2004-3

[7]
Neuroimmune interactions at different intestinal sites are related to abdominal pain symptoms in children with IBS.

Neurogastroenterol Motil. 2013-11-7

[8]
Mast cell-dependent excitation of visceral-nociceptive sensory neurons in irritable bowel syndrome.

Gastroenterology. 2007-1

[9]
New insights into the pathogenesis and treatment of irritable bowel syndrome.

Adv Med Sci. 2017-3

[10]
Mucosal permeability and immune activation as potential therapeutic targets of probiotics in irritable bowel syndrome.

J Clin Gastroenterol. 2012-10

引用本文的文献

[1]
Novel Bicyclic Heterocycles as MRGPRX2 Antagonists for Treating Inflammatory Diseases.

ACS Med Chem Lett. 2025-6-2

[2]
Novel Bicyclic Heterocycles as MRGPRX2 Antagonists for Treating Inflammatory Diseases.

ACS Med Chem Lett. 2025-4-2

[3]
Multiple Aspects of Irritable Bowel Syndrome and the Role of the Immune System: An Overview of Systematic Reviews with a Focus on Polyphenols.

Int J Mol Sci. 2024-11-8

本文引用的文献

[1]
Postprandial symptoms in disorders of gut-brain interaction and their potential as a treatment target.

Gut. 2024-6-6

[2]
Coffee, Alcohol, and Artificial Sweeteners Have Temporal Associations with Gastrointestinal Symptoms.

Dig Dis Sci. 2024-7

[3]
Fructose malabsorption and fructan malabsorption are associated in patients with irritable bowel syndrome.

BMC Gastroenterol. 2024-4-24

[4]
Treatment of non-constipated irritable bowel syndrome with the histamine 1 receptor antagonist ebastine: a randomised, double-blind, placebo-controlled trial.

Gut. 2024-2-23

[5]
What Is the Value of Counting Mast Cells in Gastrointestinal Mucosal Biopsies?

Mod Pathol. 2023-2

[6]
Inhibition of Serine Proteases as a Novel Therapeutic Strategy for Abdominal Pain in IBS.

Front Physiol. 2022-5-19

[7]
An Allergic Basis for Abdominal Pain.

N Engl J Med. 2021-6-3

[8]
Multifaceted MRGPRX2: New insight into the role of mast cells in health and disease.

J Allergy Clin Immunol. 2021-8

[9]
Impact of Diet on Symptoms of the Irritable Bowel Syndrome.

Nutrients. 2021-2-9

[10]
Local immune response to food antigens drives meal-induced abdominal pain.

Nature. 2021-2

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