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Increased NOX1 and DUOX2 expression in the colonic mucosa of patients with chronic functional constipation

To determine whether oxidative stress and inflammation are associated with constipation by examining the expression of the main producers of reactive oxygen species, nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, and pro-inflammatory cytokines in the colon of patients with chronic fun...

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Autores principales: Wei, Xiuqin, Xue, Mei, Kang, Chunbo, Gao, Lei, Zhang, Mengqiao, Ma, Chao, Jia, Wei, Zheng, Yufeng, Cao, Lei, Chen, Pan, Jiang, Shujing, Chu, Fong-Fong, Gao, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371511/
https://www.ncbi.nlm.nih.gov/pubmed/35960091
http://dx.doi.org/10.1097/MD.0000000000030028
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author Wei, Xiuqin
Xue, Mei
Kang, Chunbo
Gao, Lei
Zhang, Mengqiao
Ma, Chao
Jia, Wei
Zheng, Yufeng
Cao, Lei
Chen, Pan
Jiang, Shujing
Chu, Fong-Fong
Gao, Qiang
author_facet Wei, Xiuqin
Xue, Mei
Kang, Chunbo
Gao, Lei
Zhang, Mengqiao
Ma, Chao
Jia, Wei
Zheng, Yufeng
Cao, Lei
Chen, Pan
Jiang, Shujing
Chu, Fong-Fong
Gao, Qiang
author_sort Wei, Xiuqin
collection PubMed
description To determine whether oxidative stress and inflammation are associated with constipation by examining the expression of the main producers of reactive oxygen species, nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, and pro-inflammatory cytokines in the colon of patients with chronic functional constipation. The colonic biopsies were collected from 32 patients with chronic functional constipation and 30 healthy subjects who underwent colonoscopy. Colonic mucosal histology was observed. Interleukin (IL)-1β, IL-6, IL-8 messenger RNA (mRNA), and 4 members of NADPH oxidase (NOX1, NOX2, DUOX2, and NOX4) protein and mRNA were assessed by immunohistochemistry, western blotting, and reverse transcription polymerase chain reaction. The tissues from both patients and healthy subjects showed normal histological structure without increase of inflammatory cells. NOX1 protein and mRNA levels were significantly increased compared to controls (P < .05). DUOX2 protein, but not mRNA, was increased by 2-fold compared to controls (P < .05). The levels of NOX2 and NOX4 protein and mRNA demonstrated no significant difference between patients and control subjects. The levels of IL-1β and IL-6 mRNA were significantly higher in constipation patients (P < .05), while IL-8 mRNA level was no different between the 2 groups. NADPH oxidase and pro-inflammatory cytokine might be involved in the pathogeneses of chronic functional constipation.
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spelling pubmed-93715112022-08-16 Increased NOX1 and DUOX2 expression in the colonic mucosa of patients with chronic functional constipation Wei, Xiuqin Xue, Mei Kang, Chunbo Gao, Lei Zhang, Mengqiao Ma, Chao Jia, Wei Zheng, Yufeng Cao, Lei Chen, Pan Jiang, Shujing Chu, Fong-Fong Gao, Qiang Medicine (Baltimore) Research Article To determine whether oxidative stress and inflammation are associated with constipation by examining the expression of the main producers of reactive oxygen species, nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, and pro-inflammatory cytokines in the colon of patients with chronic functional constipation. The colonic biopsies were collected from 32 patients with chronic functional constipation and 30 healthy subjects who underwent colonoscopy. Colonic mucosal histology was observed. Interleukin (IL)-1β, IL-6, IL-8 messenger RNA (mRNA), and 4 members of NADPH oxidase (NOX1, NOX2, DUOX2, and NOX4) protein and mRNA were assessed by immunohistochemistry, western blotting, and reverse transcription polymerase chain reaction. The tissues from both patients and healthy subjects showed normal histological structure without increase of inflammatory cells. NOX1 protein and mRNA levels were significantly increased compared to controls (P < .05). DUOX2 protein, but not mRNA, was increased by 2-fold compared to controls (P < .05). The levels of NOX2 and NOX4 protein and mRNA demonstrated no significant difference between patients and control subjects. The levels of IL-1β and IL-6 mRNA were significantly higher in constipation patients (P < .05), while IL-8 mRNA level was no different between the 2 groups. NADPH oxidase and pro-inflammatory cytokine might be involved in the pathogeneses of chronic functional constipation. Lippincott Williams & Wilkins 2022-08-12 /pmc/articles/PMC9371511/ /pubmed/35960091 http://dx.doi.org/10.1097/MD.0000000000030028 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wei, Xiuqin
Xue, Mei
Kang, Chunbo
Gao, Lei
Zhang, Mengqiao
Ma, Chao
Jia, Wei
Zheng, Yufeng
Cao, Lei
Chen, Pan
Jiang, Shujing
Chu, Fong-Fong
Gao, Qiang
Increased NOX1 and DUOX2 expression in the colonic mucosa of patients with chronic functional constipation
title Increased NOX1 and DUOX2 expression in the colonic mucosa of patients with chronic functional constipation
title_full Increased NOX1 and DUOX2 expression in the colonic mucosa of patients with chronic functional constipation
title_fullStr Increased NOX1 and DUOX2 expression in the colonic mucosa of patients with chronic functional constipation
title_full_unstemmed Increased NOX1 and DUOX2 expression in the colonic mucosa of patients with chronic functional constipation
title_short Increased NOX1 and DUOX2 expression in the colonic mucosa of patients with chronic functional constipation
title_sort increased nox1 and duox2 expression in the colonic mucosa of patients with chronic functional constipation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371511/
https://www.ncbi.nlm.nih.gov/pubmed/35960091
http://dx.doi.org/10.1097/MD.0000000000030028
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