Abstract | ETHNOPHARMACOLOGICAL RELEVANCE: AIM OF THE STUDY: MATERIALS AND METHODS:
Sulfasalazine and JLC were administrated orally and initialized 6 h after TNBS enema, once a day for seven consecutive days. The effect of JLC on intestinal microbial populations and LPS/TLR-4/NF-κB pathway was observed and assessed. Thirty female SD rats were distributed into six groups randomly and equally, namely, control, TNBS, TNBS + sulfasalazine (625 mg/kg), and TNBS + three different doses of JLC (25, 50, and 100 mg/kg) groups. RESULTS: The effect of JLC on restoring normal structures of colorectum and repairing colonic damage were superior to that of sulfasalazine. JLC showed a positive effect in re-balancing intestinal bacteria population of colitis, and suppressed the activation of LPS/TLR-4/NF-κB pathway. CONCLUSION: The results suggest that JLC demonstrated a beneficial effect on treating colitis in a rat model. The possible mechanisms may be through the regulatory effect of intestinal commensal bacteria and down-regulation of LPS/TLR-4/NF-κB pathway.
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Authors | Yuhua Li, Yang Sun, Fanrong Diao, Yiming Ruan, Gui'e Chen, Tianle Tang, Yongsheng Liu, Huiping Zhou, Wenming Lin, Mingzhi Dong, Tieming Liu, Qibing Mei, De Cai |
Journal | Journal of ethnopharmacology
(J Ethnopharmacol)
Vol. 269
Pg. 113716
(Apr 06 2021)
ISSN: 1872-7573 [Electronic] Ireland |
PMID | 33352238
(Publication Type: Journal Article)
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Copyright | Copyright © 2020 Elsevier B.V. All rights reserved. |
Chemical References |
- Drugs, Chinese Herbal
- Gastrointestinal Agents
- NF-kappa B
- Protective Agents
- Rela protein, rat
- Tlr4 protein, rat
- Toll-Like Receptor 4
- Transcription Factor RelA
- NF-KappaB Inhibitor alpha
- Sulfasalazine
- Trinitrobenzenesulfonic Acid
- Cyclooxygenase 2
- Ptgs2 protein, rat
- Dinoprostone
- Acetic Acid
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Topics |
- Acetic Acid
(toxicity)
- Animals
- Behavior, Animal
(drug effects)
- Colitis, Ulcerative
(chemically induced, drug therapy)
- Colon
(drug effects, pathology)
- Cyclooxygenase 2
(genetics, metabolism)
- Dinoprostone
(metabolism)
- Disease Models, Animal
- Down-Regulation
(drug effects)
- Drugs, Chinese Herbal
(chemistry, pharmacology, therapeutic use)
- Female
- Gastrointestinal Agents
(pharmacology, therapeutic use)
- Gastrointestinal Microbiome
(drug effects)
- Mice, Inbred ICR
- NF-KappaB Inhibitor alpha
(genetics, metabolism)
- NF-kappa B
(genetics, metabolism)
- Pain
(chemically induced, drug therapy)
- Protective Agents
(chemistry, pharmacology, therapeutic use)
- Rats, Sprague-Dawley
- Signal Transduction
(drug effects)
- Sulfasalazine
(pharmacology, therapeutic use)
- Toll-Like Receptor 4
(biosynthesis, drug effects)
- Transcription Factor RelA
(genetics, metabolism)
- Trinitrobenzenesulfonic Acid
(toxicity)
- Mice
- Rats
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