4.8 Article

Total Flavonoids of Glycyrrhiza uralensis Alleviates Irinotecan-Induced Colitis via Modification of Gut Microbiota and Fecal Metabolism

Journal

FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.628358

Keywords

Glycyrrhiza uralensis; total flavonoids; CPT-11; gut microbiota; metabolomics; uric acid; NLRP3 inflammasome

Categories

Funding

  1. National Key R&D Program of China [2019YFC1711000]
  2. National Natural Science Foundation of China [81903786, 81974522]
  3. Key Research and Development Program of Shaanxi [2019ZDLSF04-05]
  4. Subject Innovation Team of Shaanxi University of Chinese Medicine [2019-YL10]
  5. Young Talent Support Program from the Association for Science and Technology of Colleges in Shaanxi Province [20190306]
  6. Shaanxi Administration of Traditional Chinese Medicine [2019-ZZ-JC018]

Ask authors/readers for more resources

Our study demonstrated that total flavonoids of Glycyrrhiza uralensis can effectively alleviate CPT-11-induced body weight loss and colon shortening in mice. Additionally, TFGU was found to restore the perturbed gut microbial structure and fecal metabolic disorders in CPT-11-treated mice.
Irinotecan (CPT-11)-induced gastrointestinal toxicity strongly limits its anticancer efficacy. Glycyrrhiza uralensis Fisch., especially flavonoids, has strong anti-inflammatory and immunomodulatory activities. Herein, we investigate the protective effect of the total flavonoids of G. uralensis (TFGU) on CPT-11-induced colitis mice from the perspective of gut microbiota and fecal metabolism. The body weight and colon length of mice were measured. Our results showed that oral administration of TFGU significantly attenuated the loss of body weight and the shortening of colon length induced by CPT-11. The elevated disease activity index and histological score of colon as well as the up-regulated mRNA and protein levels of TNF-alpha, IL-1 beta, and IL-6 in the colonic tissue of CPT-11-treated mice were significantly decreased by TFGU. Meanwhile, TFGU restored the perturbed gut microbial structure and function in CPT-11-treated mice to near normal level. TFGU also effectively reversed the CPT-11-induced fecal metabolic disorders in mice, mainly call backing the hypoxanthine and uric acid in purine metabolism. Spearman's correlation analysis further revealed that Lactobacillus abundance negatively correlated with fecal uric acid concentration, suggesting the pivotal role of gut microbiota in CPT-11-induced colitis. Since uric acid is a ligand of the NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome, TFGU was further validated to inhibit the activation of NLRP3 inflammasome by CPT-11. Our findings suggest TFGU can correct the overall gut microbial dysbiosis and fecal metabolic disorders in the CPT-11-induced colitis mice, underscoring the potential of using dietary G. uralensis as a chemotherapeutic adjuvant.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available