Ajou University repository

Sulglycotide ameliorates inflammation in lipopolysaccharide-stimulated mouse macrophage cells by blocking the NF-κB signaling pathway
Citations

SCOPUS

8

Citation Export

Publication Year
2019-01-01
Publisher
Taylor and Francis Ltd
Citation
Immunopharmacology and Immunotoxicology, Vol.41, pp.477-484
Keyword
inflammationlipopolysaccharidemacrophagereactive oxygen speciesSulglycotide
Mesh Keyword
AnimalsAnti-Inflammatory AgentsCell LineCytokinesInflammationLipopolysaccharidesMacrophagesMAP Kinase Signaling SystemMiceNF-kappa BRAW 264.7 CellsReactive Oxygen SpeciesSialoglycoproteinsSignal Transduction
All Science Classification Codes (ASJC)
Immunology and AllergyImmunologyToxicologyPharmacology
Abstract
Objective: Several studies demonstrated that sulglycotide has anti-inflammatory and anti-cancer effects. However, the effect of sulglycotide is limited to gastric mucosal tissues and cells and underlying molecular mechanisms are not clear. This study estimated the effect of sulglycotide on lipopolysaccharide (LPS)-induced inflammatory responses in the macrophage cell line, RAW 264.7 and elucidated the molecular mechanisms. Materials and methods: The inhibitory effect of sulglysotide on LPS-induced oxidative stress and inflammatory reactions were determined by Immunofluorescence staining, ELISA, Western blotting and RT-PCR. Results: Our results show that sulglycotide has the ability to inhibit inflammatory mediators and cytokine production as well as reactive oxygen species (ROS) generation. This effect can be the result from regulating the activation of nuclear factor-kappa B (NF-κB) through blocking mitogen-activated protein kinase (MAPK) intracellular signaling pathways. Conclusions: These results indicate that sulglycotide could be an anti-inflammatory and anti-oxidative compound that may be a useful candidate for treatment of inflammatory diseases.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/30789
DOI
https://doi.org/10.1080/08923973.2019.1628044
Fulltext

Type
Article
Funding
This study was supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea [grant #: HI15C1142].
Show full item record

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Park, Young-Joon Image
Park, Young-Joon박영준
Division of Pharmacy Sciences
Read More

Total Views & Downloads

File Download

  • There are no files associated with this item.