Effect of chronic restraint stress and western-diet feeding on colonic regulatory gene expression in mice.
Study Goal
The researchers aimed to assess the combined effects of Western diet-induced obesity and psychological stress on microbiome composition and colonic gene expression.
Results Summary
Western diet feeding induced obesity, worsened metabolic markers, and altered microbiome composition, while chronic restraint stress had differential effects on glucose metabolism and microbiome composition without synergistic interactions.
Population
C57BL/6J mice (n = 48)
Effective Dosage
Not specified
Duration
22 weeks of Western diet feeding
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
Western diet (WD) feeding | increase | DIO phenotype | C57BL/6J mice | - | induced | #1 |
Western diet (WD) feeding | increase | body weight | C57BL/6J mice | - | increased | #2 |
Western diet (WD) feeding | increase | metabolic markers | C57BL/6J mice | - | worsened | #3 |
Western diet (WD) feeding | neutral | microbiome composition | C57BL/6J mice | - | alterations to | #4 |
chronic restraint stressor (CRS) | decrease | body weight | C57BL/6J mice | - | reduced | #5 |
chronic restraint stressor (CRS) | neutral | glucose metabolism | C57BL/6J mice | - | differential effects on | #6 |
chronic restraint stressor (CRS) | increase | Firmicutes/Bacteroidetes ratio | WD-fed animals | - | improved | #7 |
chronic restraint stressor (CRS) | increase | Proteobacteria phyla | WD-fed animals | - | expanding | #8 |
Western diet (WD) feeding | decrease | colonic Tlr4 | WD-fed animals | p = 0.008 | significantly lower expression of | #9 |
Western diet (WD) feeding | decrease | colonic Ocln | WD-fed animals | p = 0.004 | significantly lower expression of | #10 |
Western diet (WD) feeding | decrease | colonic Cldn3 | WD-fed animals | p = 0.004 | significantly lower expression of | #11 |
Western diet (WD) feeding combined with chronic restraint stressor (CRS) | no change | colonic gene expression (Tlr4, Ocln, Cldn3) | WD-fed animals | - | no synergistic effects observed | #12 |
Western diet (WD) feeding and chronic restraint stressor (CRS) | no change | colonic downstream inflammatory mediators | C57BL/6J mice | - | No changes to expression of | #13 |
chronic restraint stressor (CRS) | increase | Cldn2 | mice exposed to CRS | p = 0.04 | higher levels of expression of | #14 |
chronic restraint stressor (CRS) | increase | bile acid receptor Nr1h4 | mice exposed to CRS | p = 0.02 | higher levels of expression of | #15 |
BACKGROUND: Diet-induced obesity (DIO) and psychological stress are significant independent regulators of gastrointestinal physiology; however, our understanding of how these two disorders influence the host-microbe interface is still poorly characterized. The aim of this study was to assess the combined influences of diet-induced obesity and psychological stress on microbiome composition and colonic gene expression. METHODS: C57BL/6J mice (n = 48) were subject to a combination of 22 weeks of Western diet (WD) feeding and a chronic restraint stressor (CRS) for the last 4 weeks of feeding. At the end of the combined intervention, microbiome composition was determined from cecal contents, and colonic tissue gene expression was assessed by multiplex analysis using NanoString nCounter System and real-time qPCR. RESULTS: WD feeding induced a DIO phenotype with increased body weight, worsened metabolic markers, and alterations to microbiome composition. CRS reduced body weight in both dietary groups while having differential effects on glucose metabolism. CRS improved the Firmicutes/Bacteroidetes ratio in WD-fed animals while expanding the Proteobacteria phyla. Significantly lower expression of colonic Tlr4 (p = 0.008), Ocln (p = 0.004), and Cldn3 (p = 0.004) were noted in WD-fed animals compared to controls with no synergistic effects observed when combined with CRS. No changes to colonic expression of downstream inflammatory mediators were observed. Interestingly, higher levels of expression of Cldn2 (p = 0.04) and bile acid receptor Nr1h4 (p = 0.02) were seen in mice exposed to CRS. CONCLUSION: Differential but not synergistic effects of WD and CRS were noted at the host-microbe interface suggesting multifactorial responses that require further investigation.