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Protective effects of patchouli alcohol against DSS-induced ulcerative colitis.

Scientific reports
July 20, 2024
Huifang Han et al. (16 authors)
Journal ArticleAnimal Study
Extracted Claims (9)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Patchouli alcohol (PA)
decrease
inflammatory response
ulcerative colitis (UC) symptoms
-
exhibited promising preventions against
#1
PA
decrease
expressions of pro-inflammatory factors, including interleukin (IL)-1β, IL-6, tumor necrosis factor-α, and chemokine ligand 5
-
-
significantly attenuated
#2
PA
increase
intestinal barrier damage
caused by dextran sodium sulfate (DSS)
-
enhanced
#3
PA
no change
DSS-induced gut microbiota dysbiosis
-
-
exhibited negligible inventions on
#4
PA
no change
diversity of the DSS gut microbiota
-
-
did not affect
#5
PA
increase
composition
DSS gut microbiota
-
altered
#6
PA
increase
Firmicutes-Bacteroidetes (F/B) ratio
-
-
significant increase in
#7
PA
decrease
expressions of heme oxygenase-1 (HO-1) and inducible nitric oxide synthase (iNOS)
DSS-treated mice
-
suppressing
#8
PA
decrease
inflammatory response
DSS-induced UC mice model
-
prevented
#9
Abstract

Patchouli alcohol (PA) is a widely used pharmaceutical ingredient in various Chinese traditional herbal medicine (THM) formulations, known for its modulatory effects on the gut microbiota. The present study investigated PA's anti-inflammatory and regulatory effects on gut microbiota and its mode of action (MOA). Based on the assessments of ulcerative colitis (UC) symptoms, PA exhibited promising preventions against inflammatory response. In accordance, the expressions of pro-inflammatory factors, including interleukin (IL)-1β, IL-6, tumor necrosis factor-α, and chemokine ligand 5 were significantly attenuated under PA treatment. Furthermore, PA enhanced the intestinal barrier damage caused by dextran sodium sulfate (DSS). Interestingly, PA exhibited negligible inventions on DSS-induced gut microbiota dysbiosis. PA did not affect the diversity of the DSS gut microbiota, it did alter the composition, as evidenced by a significant increase in the Firmicutes-Bacteroidetes (F/B) ratio. Finally, the MOA of PA against inflammation in DSS-treated mice was addressed by suppressing the expressions of heme oxygenase-1 (HO-1) and inducible nitric oxide synthase (iNOS). In conclusion, PA prevented inflammatory response in the DSS-induced UC mice model via directly suppressing HO-1 and iNOS-associated antioxidant signal pathways, independent of its effects on gut microbiota composition.

Medical Subject Headings (MeSH)
AnimalsColitis, UlcerativeDextran SulfateMiceGastrointestinal MicrobiomeDisease Models, AnimalSesquiterpenesHeme Oxygenase-1Nitric Oxide Synthase Type IIMaleAnti-Inflammatory AgentsDysbiosisMice, Inbred C57BLDrugs, Chinese Herbal
Study Links
Citation Metrics
Total Citations3
Citations/Year3.0
Research Impact Scores
APT Score0.05
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