Cargando…
Influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes
According to clinical investigations, sleep disruption (SD) can influence the immune system and cause inflammatory bowel disease (IBD). However, the detailed effects of sleep on IBD development and progression have not been clarified. Here, we used dextran sulfate sodium (DSS) to induce colitis in m...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618989/ https://www.ncbi.nlm.nih.gov/pubmed/36325141 http://dx.doi.org/10.1016/j.heliyon.2022.e11229 |
_version_ | 1784821176934072320 |
---|---|
author | Wang, Dan Yin, Houqing Wang, Xin Wang, Zequn Han, Mengyuan He, Quanzhao Chen, Jingjing Xian, Haocheng Zhang, Bentuo Wei, Xihua Yang, Baoxue Pan, Yan Li, Jun |
author_facet | Wang, Dan Yin, Houqing Wang, Xin Wang, Zequn Han, Mengyuan He, Quanzhao Chen, Jingjing Xian, Haocheng Zhang, Bentuo Wei, Xihua Yang, Baoxue Pan, Yan Li, Jun |
author_sort | Wang, Dan |
collection | PubMed |
description | According to clinical investigations, sleep disruption (SD) can influence the immune system and cause inflammatory bowel disease (IBD). However, the detailed effects of sleep on IBD development and progression have not been clarified. Here, we used dextran sulfate sodium (DSS) to induce colitis in mice, and then interfered with SD (day-time 8:00 a.m. to 5:00 p.m.) to explore the influence of sleep on colitis by analyzing colon length, mouse body weight, disease activity index (DAI) score, pathology detection, and infiltration of inflammatory cells with LCA immunohistochemistry analysis. Next, we detected the mRNA levels of circadian genes and related inflammatory factors, including Bmal1, CLOCK, Cry1, Cry2, Per1, Per2, Timeless, Rev-erbα, TNF-α, IL-6, and IFN-γ. Additionally, we conducted a sleep survey in IBD patients and collected colon lesion sites to detect the mRNA levels of those eight circadian genes and three inflammatory factors. We found that SD promoted the body weight decrease, increased inflammation as shown with pathological staining of the DSS animal model, and increased expression of the clock gene Cry2 in DSS-induced colitis mice. In IBD patients with active disease, the mRNA level of circadian genes Bmal1, Cry1, Cry2, and Rev-erbα in inflammatory tissues decreased significantly compared with non-inflammatory tissues. |
format | Online Article Text |
id | pubmed-9618989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-96189892022-11-01 Influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes Wang, Dan Yin, Houqing Wang, Xin Wang, Zequn Han, Mengyuan He, Quanzhao Chen, Jingjing Xian, Haocheng Zhang, Bentuo Wei, Xihua Yang, Baoxue Pan, Yan Li, Jun Heliyon Research Article According to clinical investigations, sleep disruption (SD) can influence the immune system and cause inflammatory bowel disease (IBD). However, the detailed effects of sleep on IBD development and progression have not been clarified. Here, we used dextran sulfate sodium (DSS) to induce colitis in mice, and then interfered with SD (day-time 8:00 a.m. to 5:00 p.m.) to explore the influence of sleep on colitis by analyzing colon length, mouse body weight, disease activity index (DAI) score, pathology detection, and infiltration of inflammatory cells with LCA immunohistochemistry analysis. Next, we detected the mRNA levels of circadian genes and related inflammatory factors, including Bmal1, CLOCK, Cry1, Cry2, Per1, Per2, Timeless, Rev-erbα, TNF-α, IL-6, and IFN-γ. Additionally, we conducted a sleep survey in IBD patients and collected colon lesion sites to detect the mRNA levels of those eight circadian genes and three inflammatory factors. We found that SD promoted the body weight decrease, increased inflammation as shown with pathological staining of the DSS animal model, and increased expression of the clock gene Cry2 in DSS-induced colitis mice. In IBD patients with active disease, the mRNA level of circadian genes Bmal1, Cry1, Cry2, and Rev-erbα in inflammatory tissues decreased significantly compared with non-inflammatory tissues. Elsevier 2022-10-21 /pmc/articles/PMC9618989/ /pubmed/36325141 http://dx.doi.org/10.1016/j.heliyon.2022.e11229 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Wang, Dan Yin, Houqing Wang, Xin Wang, Zequn Han, Mengyuan He, Quanzhao Chen, Jingjing Xian, Haocheng Zhang, Bentuo Wei, Xihua Yang, Baoxue Pan, Yan Li, Jun Influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes |
title | Influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes |
title_full | Influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes |
title_fullStr | Influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes |
title_full_unstemmed | Influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes |
title_short | Influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes |
title_sort | influence of sleep disruption on inflammatory bowel disease and changes in circadian rhythm genes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618989/ https://www.ncbi.nlm.nih.gov/pubmed/36325141 http://dx.doi.org/10.1016/j.heliyon.2022.e11229 |
work_keys_str_mv | AT wangdan influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT yinhouqing influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT wangxin influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT wangzequn influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT hanmengyuan influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT hequanzhao influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT chenjingjing influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT xianhaocheng influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT zhangbentuo influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT weixihua influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT yangbaoxue influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT panyan influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes AT lijun influenceofsleepdisruptiononinflammatoryboweldiseaseandchangesincircadianrhythmgenes |