Chronic Gut Inflammation and Dysbiosis in IBS: Unraveling Their Contribution to Atopic Dermatitis Progression.
Jae-Hwan JangSun-Young JangSora AhnJu-Young OhMijung YeomSeok-Jae KoJae-Woo ParkSoon-Kyeong KwonKyuseok KimIn-Seon LeeDae-Hyun HahmHi-Joon ParkPublished in: International journal of molecular sciences (2024)
Emerging evidence suggests a link between atopic dermatitis (AD) and gastrointestinal disorders, particularly in relation to gut microbial dysbiosis. This study explored the potential exacerbation of AD by gut inflammation and microbial imbalances using an irritable bowel syndrome (IBS) mouse model. Chronic gut inflammation was induced in the model by intrarectal injection of 2,4,6-trinitrobenzene sulfonic acid (TNBS), followed by a 4-week development period. We noted significant upregulation of proinflammatory cytokines in the colon and evident gut microbial dysbiosis in the IBS mice. Additionally, these mice exhibited impaired gut barrier function, increased permeability, and elevated systemic inflammation markers such as IL-6 and LPS. A subsequent MC903 challenge on the right cheek lasting for 7 days revealed more severe AD symptoms in IBS mice compared to controls. Further, fecal microbial transplantation (FMT) from IBS mice resulted in aggravated AD symptoms, a result similarly observed with FMT from an IBS patient. Notably, an increased abundance of Alistipes in the feces of IBS mice correlated with heightened systemic and localized inflammation in both the gut and skin. These findings collectively indicate that chronic gut inflammation and microbial dysbiosis in IBS are critical factors exacerbating AD, highlighting the integral relationship between gut and skin health.
Keyphrases
- irritable bowel syndrome
- oxidative stress
- microbial community
- high fat diet induced
- atopic dermatitis
- mouse model
- healthcare
- type diabetes
- clinical trial
- drug induced
- intensive care unit
- inflammatory response
- stem cells
- depressive symptoms
- risk assessment
- adipose tissue
- climate change
- wild type
- signaling pathway
- ultrasound guided
- long non coding rna
- acute respiratory distress syndrome
- extracorporeal membrane oxygenation