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黏膜胆汁酸谱的改变与腹泻型肠易激综合征患者肥大细胞中神经生长因子的表达及肠道症状相关。

The alteration of mucosal bile acid profile is associated with nerve growth factor expression in mast cells and bowel symptoms in diarrhea-predominant irritable bowel syndrome.

作者信息

Wu Bi-Yu, Xu Ping, Cheng Li, Wang Qian-Qian, Qiu Hong-Yi, Yan Xiu-Juan, Chen Sheng-Liang

机构信息

Division of Gastroenterology and Hepatology, NHC Key Laboratory of Digestive Diseases, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Institute of Digestive Disease, Shanghai, China.

出版信息

Clin Exp Immunol. 2024 Apr 23;216(2):200-210. doi: 10.1093/cei/uxae006.


DOI:10.1093/cei/uxae006
PMID:38290436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11036107/
Abstract

Mucosal bile acid (BA) profile is still unestablished in diarrhea-predominant irritable bowel syndrome (IBS-D). The aim of this study was to explore colonic mucosal BAs and their associations with mucosal mast cell (MMC)-derived nerve growth factor (NGF) and bowel symptoms in IBS-D. Colonic mucosal biopsies from 36 IBS-D patients and 35 healthy controls (HCs) were obtained for targeted BA profiling. MMC count and the expression of NGF and tight junction proteins (TJPs) were examined. We found that colonic mucosal BA profile was altered in the IBS-D cohort. The proportion of primary BAs was significantly higher and that of secondary BAs was lower in IBS-D patients. According to the 90th percentile of total mucosal BA content of HCs, IBS-D patients were divided into BA-H (n = 7, 19.4%) and BA-L (n = 29, 80.6%) subgroups. BA-H patients showed significantly higher total mucosal BA content compared to BA-L subgroup and HCs. The mucosal content of 11 BA metabolites significantly increased in BA-H subgroup, e.g. cholic acid (CA) and taurocholic acid (TCA). Moreover, BA-H patients displayed significantly elevated MMC count and NGF expression, with decreased expression of TJPs (claudin-1, junctional adhesion molecule-A and zonula occludens-1). Correlation analyses revealed that mucosal TCA content positively correlated with MMC count, MMC-derived NGF levels, and abdominal pain while negatively correlated with TJP expression. In conclusion, IBS-D patients showed an altered BA profile in the colonic mucosa. Approximately 20% of them exhibit elevated mucosal BA content, which may be associated with MMC-derived NGF signaling and bowel symptoms.

摘要

腹泻型肠易激综合征(IBS-D)患者的黏膜胆汁酸(BA)谱仍未明确。本研究旨在探讨IBS-D患者结肠黏膜中的BA及其与黏膜肥大细胞(MMC)衍生的神经生长因子(NGF)和肠道症状的关系。收集了36例IBS-D患者和35例健康对照者(HCs)的结肠黏膜活检组织进行靶向BA分析。检测了MMC计数以及NGF和紧密连接蛋白(TJPs)的表达。我们发现IBS-D队列中结肠黏膜BA谱发生了改变。IBS-D患者中初级BA的比例显著更高,次级BA的比例更低。根据HCs黏膜总BA含量的第90百分位数,将IBS-D患者分为BA-H(n = 7,19.4%)和BA-L(n = 29,80.6%)亚组。与BA-L亚组和HCs相比,BA-H患者的黏膜总BA含量显著更高。BA-H亚组中11种BA代谢产物的黏膜含量显著增加,如胆酸(CA)和牛磺胆酸(TCA)。此外,BA-H患者的MMC计数和NGF表达显著升高,而TJPs(闭合蛋白-1、连接黏附分子-A和闭锁小带-1)的表达降低。相关性分析显示,黏膜TCA含量与MMC计数、MMC衍生的NGF水平和腹痛呈正相关,而与TJP表达呈负相关。总之,IBS-D患者结肠黏膜中的BA谱发生了改变。其中约20%的患者黏膜BA含量升高,这可能与MMC衍生的NGF信号传导和肠道症状有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c68e/11036107/aedeb55d0b88/uxae006_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c68e/11036107/aedeb55d0b88/uxae006_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c68e/11036107/aedeb55d0b88/uxae006_fig6.jpg

相似文献

[1]
The alteration of mucosal bile acid profile is associated with nerve growth factor expression in mast cells and bowel symptoms in diarrhea-predominant irritable bowel syndrome.

Clin Exp Immunol. 2024-4-23

[2]
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FASEB J. 2018-9-27

[3]
Nerve growth factor content is increased in the rectal mucosa of children with diarrhea-predominant irritable bowel syndrome.

Neurogastroenterol Motil. 2012-5-24

[4]
Colonic mucosal gene expression and genotype in irritable bowel syndrome patients with normal or elevated fecal bile acid excretion.

Am J Physiol Gastrointest Liver Physiol. 2015-7-1

[5]
The function of the gut microbiota-bile acid-TGR5 axis in diarrhea-predominant irritable bowel syndrome.

mSystems. 2024-3-19

[6]
Diarrhoea-predominant irritable bowel syndrome: an organic disorder with structural abnormalities in the jejunal epithelial barrier.

Gut. 2012-5-25

[7]
Altered metabolism of bile acids correlates with clinical parameters and the gut microbiota in patients with diarrhea-predominant irritable bowel syndrome.

World J Gastroenterol. 2020-12-7

[8]
Increased intestinal mucosal leptin levels in patients with diarrhea-predominant irritable bowel syndrome.

World J Gastroenterol. 2018-1-7

[9]
Effect of increased bile acid synthesis or fecal excretion in irritable bowel syndrome-diarrhea.

Am J Gastroenterol. 2014-10

[10]
Intestinal serotonin release, sensory neuron activation, and abdominal pain in irritable bowel syndrome.

Am J Gastroenterol. 2011-3-22

本文引用的文献

[1]
The Gut Microbial Bile Acid Modulation and Its Relevance to Digestive Health and Diseases.

Gastroenterology. 2023-6

[2]
Understanding neuroimmune interactions in disorders of gut-brain interaction: from functional to immune-mediated disorders.

Gut. 2023-4

[3]
Bile Acid and Gut Microbiota in Irritable Bowel Syndrome.

J Neurogastroenterol Motil. 2022-10-30

[4]
AGA Clinical Practice Guideline on the Pharmacological Management of Irritable Bowel Syndrome With Diarrhea.

Gastroenterology. 2022-7

[5]
Comparison of biochemical, microbial and mucosal mRNA expression in bile acid diarrhoea and irritable bowel syndrome with diarrhoea.

Gut. 2023-1

[6]
Bile acid-gut microbiota crosstalk in irritable bowel syndrome.

Crit Rev Microbiol. 2023-5

[7]
Mast cell mediation of visceral sensation and permeability in irritable bowel syndrome.

Neurogastroenterol Motil. 2022-7

[8]
Gut microbiota-derived bile acids in intestinal immunity, inflammation, and tumorigenesis.

Cell Host Microbe. 2022-3-9

[9]
Bile acid detergency: permeability, inflammation, and effects of sulfation.

Am J Physiol Gastrointest Liver Physiol. 2022-5-1

[10]
Aberrant Gut-To-Brain Signaling in Irritable Bowel Syndrome - The Role of Bile Acids.

Front Endocrinol (Lausanne). 2021

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