Sophie Fowler, Gemma M Paech, Emily C Hoedt, Jennifer C Pryor, Cheenie Nieva, Jessica K Bruce, Prema M Nair, Guy D Eslick, Simonne Sherwin, Peter Pockney, Nicholas J Talley, Grace L Burns, Simon Keely
{"title":"外周CRY1基因表达的改变可能与器质性和功能性胃肠道疾病有关。","authors":"Sophie Fowler, Gemma M Paech, Emily C Hoedt, Jennifer C Pryor, Cheenie Nieva, Jessica K Bruce, Prema M Nair, Guy D Eslick, Simonne Sherwin, Peter Pockney, Nicholas J Talley, Grace L Burns, Simon Keely","doi":"10.1113/EP092725","DOIUrl":null,"url":null,"abstract":"<p><p>Gastrointestinal conditions such as irritable bowel syndrome (IBS) and inflammatory bowel diseases (IBD) are characterized by alterations in physiological and immune functions. Given the circadian clock influences gastrointestinal physiology and immunity, we hypothesized that the peripheral circadian clock is altered in these patients and might contribute to immune activation associated with IBD and IBS. To investigate this, RNA was extracted from whole blood obtained from control subjects (n = 29), IBD (n = 40 ulcerative colitis, n = 38 Crohn's disease) and IBS (n = 38) participants to investigate peripheral clock gene expression via quantitative PCR. A linear regression model was used to assess the impact of the time of blood collection on clock gene expression. Self-reported data regarding fatigue and sleep indices were compared between patients and control subjects. Gene expression analysis revealed variations in the peripheral circadian system between IBD, IBS and control subjects. The core clock gene CRY1 had higher relative expression in IBS (p = 0.031) and ulcerative colitis patients (p = 0.042) compared with control subjects. Patients with gastrointestinal disease demonstrated poorer quality sleep (IBS p < 0.001, UC p = 0.025 and CD p = 0.007) and more troublesome sleep (IBS p < 0.001, UC p = 0.002 and CD p = 0.009) compared with control subjects. These data suggest a role for CRY1 gene expression in patients experiencing fatigue and highlight a link between circadian dysregulation and the pathophysiology of intestinal disease.</p>","PeriodicalId":12092,"journal":{"name":"Experimental Physiology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Altered peripheral CRY1 gene expression may contribute to both organic and functional gastrointestinal disease.\",\"authors\":\"Sophie Fowler, Gemma M Paech, Emily C Hoedt, Jennifer C Pryor, Cheenie Nieva, Jessica K Bruce, Prema M Nair, Guy D Eslick, Simonne Sherwin, Peter Pockney, Nicholas J Talley, Grace L Burns, Simon Keely\",\"doi\":\"10.1113/EP092725\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Gastrointestinal conditions such as irritable bowel syndrome (IBS) and inflammatory bowel diseases (IBD) are characterized by alterations in physiological and immune functions. Given the circadian clock influences gastrointestinal physiology and immunity, we hypothesized that the peripheral circadian clock is altered in these patients and might contribute to immune activation associated with IBD and IBS. To investigate this, RNA was extracted from whole blood obtained from control subjects (n = 29), IBD (n = 40 ulcerative colitis, n = 38 Crohn's disease) and IBS (n = 38) participants to investigate peripheral clock gene expression via quantitative PCR. A linear regression model was used to assess the impact of the time of blood collection on clock gene expression. Self-reported data regarding fatigue and sleep indices were compared between patients and control subjects. Gene expression analysis revealed variations in the peripheral circadian system between IBD, IBS and control subjects. The core clock gene CRY1 had higher relative expression in IBS (p = 0.031) and ulcerative colitis patients (p = 0.042) compared with control subjects. Patients with gastrointestinal disease demonstrated poorer quality sleep (IBS p < 0.001, UC p = 0.025 and CD p = 0.007) and more troublesome sleep (IBS p < 0.001, UC p = 0.002 and CD p = 0.009) compared with control subjects. These data suggest a role for CRY1 gene expression in patients experiencing fatigue and highlight a link between circadian dysregulation and the pathophysiology of intestinal disease.</p>\",\"PeriodicalId\":12092,\"journal\":{\"name\":\"Experimental Physiology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-08-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Experimental Physiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1113/EP092725\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHYSIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental Physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1113/EP092725","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
Altered peripheral CRY1 gene expression may contribute to both organic and functional gastrointestinal disease.
Gastrointestinal conditions such as irritable bowel syndrome (IBS) and inflammatory bowel diseases (IBD) are characterized by alterations in physiological and immune functions. Given the circadian clock influences gastrointestinal physiology and immunity, we hypothesized that the peripheral circadian clock is altered in these patients and might contribute to immune activation associated with IBD and IBS. To investigate this, RNA was extracted from whole blood obtained from control subjects (n = 29), IBD (n = 40 ulcerative colitis, n = 38 Crohn's disease) and IBS (n = 38) participants to investigate peripheral clock gene expression via quantitative PCR. A linear regression model was used to assess the impact of the time of blood collection on clock gene expression. Self-reported data regarding fatigue and sleep indices were compared between patients and control subjects. Gene expression analysis revealed variations in the peripheral circadian system between IBD, IBS and control subjects. The core clock gene CRY1 had higher relative expression in IBS (p = 0.031) and ulcerative colitis patients (p = 0.042) compared with control subjects. Patients with gastrointestinal disease demonstrated poorer quality sleep (IBS p < 0.001, UC p = 0.025 and CD p = 0.007) and more troublesome sleep (IBS p < 0.001, UC p = 0.002 and CD p = 0.009) compared with control subjects. These data suggest a role for CRY1 gene expression in patients experiencing fatigue and highlight a link between circadian dysregulation and the pathophysiology of intestinal disease.
期刊介绍:
Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged.
Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.