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Dual effects of a high-protein diet on DSS-treated mice during colitis resolution phase.

American journal of physiology. Gastrointestinal and liver physiology
October 1, 2016
Annaïg Lan et al. (10 authors)
Journal ArticleResearch Support, Non-U.S. Gov'tAnimal Study
Study Details

Study Goal

The researchers aimed to determine the impact of a high-protein diet on colonic mucosal inflammation and recovery in DSS-treated mice.

Results Summary

The high-protein diet showed deleterious effects during the post-induction phase of colitis, including higher inflammation intensity and mortality, but was associated with enhanced colonic epithelium restoration in surviving animals.

Population

DSS-treated mice (animal model of colitis).

Effective Dosage

Not specified (isocaloric high-protein diet).

Duration

19 days (5-day DSS treatment + 14-day recovery).

Interactions

None mentioned.

Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
high-protein (HP) isocaloric diet
increase
inflammation intensity
DSS-treated mice
-
was higher
#1
high-protein (HP) isocaloric diet
increase
inflammatory score
DSS-treated mice
-
higher
#2
high-protein (HP) isocaloric diet
increase
body weight loss
DSS-treated mice
-
higher
#3
high-protein (HP) isocaloric diet
increase
mortality rate
DSS-treated mice
-
higher
#4
high-protein (HP) isocaloric diet
increase
colonic crypt height
surviving animals
-
an increase
#5
high-protein (HP) isocaloric diet
increase
number of colon epithelial cells per crypt
surviving animals
-
higher
#6
high-protein (HP) isocaloric diet
increase
TGF-β3 content
surviving animals
-
higher
#7
high-protein (HP) isocaloric diet
neutral
colonic expression patterns of tight junction proteins and E-cadherin
DSS-treated mice
-
different
#8
high-protein (HP) isocaloric diet
neutral
post-induction phase
DSS-treated mice
-
showed deleterious effects
#9
high-protein (HP) isocaloric diet
neutral
colonic crypt repair after acute inflammation
surviving animals
-
associated with morphological and biochemical differences compatible with higher colonic epithelium restoration
#10
Abstract

The impact of the dietary protein level on the process of colonic mucosal inflammation and subsequent recovery remains largely unknown. In this study, we fed DSS-treated mice with either a normoproteic (NP) or a high-protein (HP) isocaloric diet from the beginning of the 5-day dextran sulfate sodium (DSS) treatment to 14 days later. Measurements of colitis indicators (colon weight:length ratio, myeloperoxidase activity, cytokine expressions) showed a similar level of colonic inflammation in both DSS groups during the colitis induction phase. However, during the colitis resolution phase, inflammation intensity was higher in the DSS-HP group than in the DSS-NP group as evidenced by higher inflammatory score and body weight loss. This coincided with a higher mortality rate. In surviving animals, an increase in colonic crypt height associated with a higher number of colon epithelial cells per crypt, and TGF-β3 content was observed in the DSS-HP vs. DSS-NP group. Moreover, colonic expression patterns of tight junction proteins and E-cadherin were also different according to the diet. Altogether, our results indicate that the HP diet, when given during both the induction and resolution periods of DSS-induced colitis, showed deleterious effects during the post-induction phase. However, HP diet ingestion was also associated with morphological and biochemical differences compatible with higher colonic epithelium restoration in surviving animals, indicating an effect of the dietary protein level on colonic crypt repair after acute inflammation. These data highlight the potential impact of the dietary protein amount during the colitis course.

Medical Subject Headings (MeSH)
AnimalsColitisColonDextran SulfateDietary ProteinsDisease Models, AnimalHumansInflammationIntestinal MucosaMaleMiceTransforming Growth Factor beta3
Study Links
Quality Scores
Safety30
Efficacy60/10
Quality75/10
Citation Metrics
Total Citations16
Citations/Year1.8
Relative Citation Ratio0.62
NIH Percentile33.5%
Research Impact Scores
APT Score0.25
Weight Score0.88
Normalized Score0.51
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