International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 289, P. 138844 - 138844
Published: Dec. 18, 2024
Language: Английский
International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 289, P. 138844 - 138844
Published: Dec. 18, 2024
Language: Английский
International Immunopharmacology, Journal Year: 2024, Volume and Issue: 130, P. 111800 - 111800
Published: March 1, 2024
Language: Английский
Citations
3Biomedical Chromatography, Journal Year: 2024, Volume and Issue: 38(6)
Published: March 14, 2024
Qingxuan Zhike granules (QXZKG), a traditional Chinese patent medication, has shown therapeutic potential against acute lung injury (ALI). However, the precise mechanism underlying its lung-protective effects requires further investigation. In this study, integrated network pharmacology, molecular docking, and lipidomics were used to elucidate QXZKG's regulatory effect on lipid metabolism in lipopolysaccharide-induced ALI. Animal experiments conducted substantiate efficacy of QXZKG reducing pro-inflammatory cytokines mitigating pulmonary pathology. Network pharmacology analysis identified 145 active compounds that directly targeted 119 primary targets Gene Ontology function emphasized roles mitogen-activated protein kinase (MAPK) cascade as crucial biological processes. The MAPK1 exhibited promising affinities for naringenin, luteolin, kaempferol. Lipidomic revealed 12 lipids showed significant restoration following treatment (p < 0.05, FC >1.2 or <0.83). Specifically, DG 38:4, 40:7, PC O-40:8, TG 18:1_18:3_22:6, PI 18:2_20:4, FA 16:3, 20:3, 20:4, 22:5, 24:5 downregulated, while Cer 18:0;2O/24:0 SM 36:1;2O/34:5 upregulated versus model groups. This study enhances our understanding QXZKG, well
Language: Английский
Citations
2International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 274, P. 133422 - 133422
Published: June 24, 2024
Small extracellular vesicles derived from milk (Milk-sEVs) have the advantages of easy availability, low cost, toxicity, and inhibition inflammation. CD36 mediates inflammation stress in a variety disease states. The purpose this study was to investigate role Milk-sEVs inhibiting fibroblast through provide reference data for treatment chronic apical periodontitis.
Language: Английский
Citations
2Journal of Applied Toxicology, Journal Year: 2024, Volume and Issue: 44(12), P. 1949 - 1961
Published: Aug. 14, 2024
Abstract Pneumonia is a serious and life‐threatening lung inflammation with high morbidity mortality. Accumulating evidence has suggested that esculin, derivative of coumarin, possesses potent anti‐inflammatory effects. This study designed to explore the pharma role underlying mechanism esculin against lipopolysaccharides (LPS)‐induced pneumonia. TC‐1 cells were stimulated by LPS mimic inflammatory injury model in vitro . Cell viability, proliferation, apoptosis determined using MTT assay, 5‐ethynyl‐2′‐deoxyuridine flow cytometry. Interleukin‐1β tumor necrosis factor α levels analyzed an enzyme‐linked immunosorbent assay. Reactive oxygen species superoxide dismutase examined special assay kits. Macrophage polarization was detected Mitogen‐activated protein kinase 14 (MAPK14) level real‐time quantitative polymerase chain reaction. MAPK14 ubiquitin‐specific protease 7 (USP7) western blot After Ubibrowser database prediction, interaction between USP7 verified Co‐immunoprecipitation The biological LPS‐challenged ALI mice vivo Here, we found significantly relieved LPS‐induced cell proliferation inhibition, apoptosis, response, oxidative stress, M1‐type macrophage promotion. expressions enhanced LPS‐treated cells, which partly abolished treatment. Overexpressing attenuated repression on LPS‐triggered injury. At molecular level, interacted maintained its stability removing ubiquitin. Moreover, repressed progression pneumonia regulating MAPK14. Taken together, exposure could mitigate targeting USP7/MAPK14 axis, providing better understanding therapeutics for
Language: Английский
Citations
2International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 289, P. 138844 - 138844
Published: Dec. 18, 2024
Language: Английский
Citations
2