Protective effects of patchouli alcohol against DSS-induced ulcerative colitis.
Huifang HanMin GaoFanghong WangZheng LuoXuejun JiangYu QiuJunhao SuXinhao DuanShiyue LuoShixin TangAhmad KhanZhen ZouChengzhi ChenQi YinJing-Fu QiuHongyang ZhangPublished in: Scientific reports (2024)
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.
Keyphrases
- inflammatory response
- nitric oxide synthase
- ulcerative colitis
- oxidative stress
- high glucose
- anti inflammatory
- diabetic rats
- lipopolysaccharide induced
- rheumatoid arthritis
- drug induced
- type diabetes
- transcription factor
- endothelial cells
- depressive symptoms
- adipose tissue
- lps induced
- immune response
- signaling pathway
- mass spectrometry
- skeletal muscle
- insulin resistance
- atomic force microscopy
- high speed