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Oxidative stress, hormones, and effects of natural antioxidants on intestinal inflammation in inflammatory bowel disease.

Frontiers in endocrinology
January 1, 2023
Dipak Kumar Sahoo et al. (7 authors)
Journal ArticleReviewHuman Study
Study Details

Study Goal

The researchers aimed to review the potential of various phytochemicals, including flaxseed oil, in targeting cellular signaling pathways to reduce intestinal inflammation in IBD.

Results Summary

The abstract suggests that flaxseed oil, among other natural compounds, may help reduce intestinal inflammation by modulating antioxidant and anti-inflammatory pathways, though specific results for flaxseed are not detailed.

Population

Not specified (general discussion of IBD patients).

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (7)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Natural antioxidant compounds
increase
ROS scavenging, antioxidant defense capacity, pro-oxidative enzymes
-
-
exhibit ROS scavenging and increase antioxidant defense capacity to inhibit pro-oxidative enzymes
#1
polyphenolic substances (such as resveratrol, curcumin, quercetin, green tea flavonoids, caffeic acid phenethyl ester, luteolin, xanthohumol, genistein, alpinetin, proanthocyanidins, anthocyanins, silymarin)
decrease
intestinal inflammation
IBD
-
target cellular signaling pathways to reduce intestinal inflammation
#2
phenolic compounds including thymol
decrease
intestinal inflammation
IBD
-
target cellular signaling pathways to reduce intestinal inflammation
#3
alkaloids such as berberine
decrease
intestinal inflammation
IBD
-
target cellular signaling pathways to reduce intestinal inflammation
#4
storage polysaccharides such as tamarind xyloglucan
decrease
intestinal inflammation
IBD
-
target cellular signaling pathways to reduce intestinal inflammation
#5
other phytochemicals represented by isothiocyanate sulforaphane and food/spices (such as ginger, flaxseed oil)
decrease
intestinal inflammation
IBD
-
target cellular signaling pathways to reduce intestinal inflammation
#6
antioxidant hormones like melatonin
decrease
intestinal inflammation
IBD
-
target cellular signaling pathways to reduce intestinal inflammation
#7
Abstract

Inflammatory bowel disease (IBD) is a chronic, relapsing gastrointestinal (GI) disorder characterized by intestinal inflammation. The etiology of IBD is multifactorial and results from a complex interplay between mucosal immunity, environmental factors, and host genetics. Future therapeutics for GI disorders, including IBD, that are driven by oxidative stress require a greater understanding of the cellular and molecular mechanisms mediated by reactive oxygen species (ROS). In the GI tract, oxidative stressors include infections and pro-inflammatory responses, which boost ROS generation by promoting the production of pro-inflammatory cytokines. Nuclear factor kappa B (NF-κB) and nuclear factor erythroid 2-related factor 2 (Nrf2) represent two important signaling pathways in intestinal immune cells that regulate numerous physiological processes, including anti-inflammatory and antioxidant activities. Natural antioxidant compounds exhibit ROS scavenging and increase antioxidant defense capacity to inhibit pro-oxidative enzymes, which may be useful in IBD treatment. In this review, we discuss various polyphenolic substances (such as resveratrol, curcumin, quercetin, green tea flavonoids, caffeic acid phenethyl ester, luteolin, xanthohumol, genistein, alpinetin, proanthocyanidins, anthocyanins, silymarin), phenolic compounds including thymol, alkaloids such as berberine, storage polysaccharides such as tamarind xyloglucan, and other phytochemicals represented by isothiocyanate sulforaphane and food/spices (such as ginger, flaxseed oil), as well as antioxidant hormones like melatonin that target cellular signaling pathways to reduce intestinal inflammation occurring with IBD.

Medical Subject Headings (MeSH)
HumansAntioxidantsReactive Oxygen SpeciesAnthocyaninsOxidative StressInflammatory Bowel DiseasesHormonesInflammation
Study Links
Quality Scores
SafetyNot Assessed
Efficacy70/10
Quality80/10
Citation Metrics
Total Citations113
Citations/Year56.5
Relative Citation Ratio29.40
NIH Percentile99.7%
Research Impact Scores
APT Score0.75
Weight Score3.35
Normalized Score0.64
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