Methyl 3-Bromo-4,5-dihydroxybenzoate Attenuates Inflammatory Bowel Disease by Regulating TLR/NF-κB Pathways.

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Autores principales: Huang, Jing, Li, Lei, Xu, Liyan, Feng, Lixin, Wang, Yuxin, Sik, Attila Gabor, Jin, Meng, Wang, Rongchun, Liu, Kechun, Li, Xiaobin
Formato: Artículo científico
Lenguaje:en
Publicado: Marine drugs 2025
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author Huang, Jing
Li, Lei
Xu, Liyan
Feng, Lixin
Wang, Yuxin
Sik, Attila Gabor
Jin, Meng
Wang, Rongchun
Liu, Kechun
Li, Xiaobin
author_facet Huang, Jing
Li, Lei
Xu, Liyan
Feng, Lixin
Wang, Yuxin
Sik, Attila Gabor
Jin, Meng
Wang, Rongchun
Liu, Kechun
Li, Xiaobin
Huang, Jing
Li, Lei
Xu, Liyan
Feng, Lixin
Wang, Yuxin
Sik, Attila Gabor
Jin, Meng
Wang, Rongchun
Liu, Kechun
Li, Xiaobin
collection PubMed - marine biology
contents Methyl 3-Bromo-4,5-dihydroxybenzoate Attenuates Inflammatory Bowel Disease by Regulating TLR/NF-κB Pathways. Huang, Jing Li, Lei Xu, Liyan Feng, Lixin Wang, Yuxin Sik, Attila Gabor Jin, Meng Wang, Rongchun Liu, Kechun Li, Xiaobin Animals Zebrafish NF-kappa B Inflammatory Bowel Diseases Signal Transduction Anti-Inflammatory Agents Disease Models, Animal Toll-Like Receptors Hydroxybenzoates Molecular Docking Simulation Trinitrobenzenesulfonic Acid Aquatic Organisms Inflammatory bowel disease (IBD) is characterized by uncontrolled, chronic relapsing inflammation in the gastrointestinal tract and has become a global healthcare problem. Here, we aimed to illustrate the anti-inflammatory activity and the underlying mechanism of methyl 3-bromo-4,5-dihydroxybenzoate (MBD), a compound derived from marine organisms, especially in IBD, using a zebrafish model. The results indicated that MBD could inhibit the inflammatory responses induced by CuSO, tail amputation and LPS in zebrafish. Furthermore, MBD notably inhibited the intestinal migration of immune cells, enhanced the integrity of the gut mucosal barrier and improved intestinal peristalsis function in a zebrafish IBD model induced by trinitro-benzene-sulfonic acid (TNBS). In addition, MBD could inhibit ROS elevation induced by TNBS. Network pharmacology analysis, molecular docking, transcriptomics sequencing and RT-PCR were conducted to investigate the potential mechanism. The results showed that MBD could regulate the TLR/NF-κB pathways by inhibiting the mRNA expression of , , , , , , , , , , , , , , and , and promoting the mRNA expression of , and In conclusion, these findings indicate that MBD could be a potential candidate for the treatment of IBD.
format Artículo científico
id pubmed_39852549
institution PubMed
language en
publishDate 2025
publisher Marine drugs
record_format pubmed
spellingShingle Methyl 3-Bromo-4,5-dihydroxybenzoate Attenuates Inflammatory Bowel Disease by Regulating TLR/NF-κB Pathways.
Huang, Jing
Li, Lei
Xu, Liyan
Feng, Lixin
Wang, Yuxin
Sik, Attila Gabor
Jin, Meng
Wang, Rongchun
Liu, Kechun
Li, Xiaobin
Animals
Zebrafish
NF-kappa B
Inflammatory Bowel Diseases
Signal Transduction
Anti-Inflammatory Agents
Disease Models, Animal
Toll-Like Receptors
Hydroxybenzoates
Molecular Docking Simulation
Trinitrobenzenesulfonic Acid
Aquatic Organisms
Methyl 3-Bromo-4,5-dihydroxybenzoate Attenuates Inflammatory Bowel Disease by Regulating TLR/NF-κB Pathways. Huang, Jing Li, Lei Xu, Liyan Feng, Lixin Wang, Yuxin Sik, Attila Gabor Jin, Meng Wang, Rongchun Liu, Kechun Li, Xiaobin Animals Zebrafish NF-kappa B Inflammatory Bowel Diseases Signal Transduction Anti-Inflammatory Agents Disease Models, Animal Toll-Like Receptors Hydroxybenzoates Molecular Docking Simulation Trinitrobenzenesulfonic Acid Aquatic Organisms Inflammatory bowel disease (IBD) is characterized by uncontrolled, chronic relapsing inflammation in the gastrointestinal tract and has become a global healthcare problem. Here, we aimed to illustrate the anti-inflammatory activity and the underlying mechanism of methyl 3-bromo-4,5-dihydroxybenzoate (MBD), a compound derived from marine organisms, especially in IBD, using a zebrafish model. The results indicated that MBD could inhibit the inflammatory responses induced by CuSO, tail amputation and LPS in zebrafish. Furthermore, MBD notably inhibited the intestinal migration of immune cells, enhanced the integrity of the gut mucosal barrier and improved intestinal peristalsis function in a zebrafish IBD model induced by trinitro-benzene-sulfonic acid (TNBS). In addition, MBD could inhibit ROS elevation induced by TNBS. Network pharmacology analysis, molecular docking, transcriptomics sequencing and RT-PCR were conducted to investigate the potential mechanism. The results showed that MBD could regulate the TLR/NF-κB pathways by inhibiting the mRNA expression of , , , , , , , , , , , , , , and , and promoting the mRNA expression of , and In conclusion, these findings indicate that MBD could be a potential candidate for the treatment of IBD.
title Methyl 3-Bromo-4,5-dihydroxybenzoate Attenuates Inflammatory Bowel Disease by Regulating TLR/NF-κB Pathways.
topic Animals
Zebrafish
NF-kappa B
Inflammatory Bowel Diseases
Signal Transduction
Anti-Inflammatory Agents
Disease Models, Animal
Toll-Like Receptors
Hydroxybenzoates
Molecular Docking Simulation
Trinitrobenzenesulfonic Acid
Aquatic Organisms
url https://pubmed.ncbi.nlm.nih.gov/39852549/