Your browser doesn't support javascript.
loading
: 20 | 50 | 100
1 - 3 de 3
1.
Chem Biodivers ; 20(3): e202201237, 2023 Mar.
Article En | MEDLINE | ID: mdl-36740572

Artemisia annua L. is a Chinese medicinal herb, but the origin of its pharmacological properties, including its anti-inflammatory activity, remain unknown. In this study, five new monoterpene glycosides (1-5) and two new sesquiterpene glycosides (6 and 7) were isolated from the aqueous extract of the aerial parts of A. annua. The structures of these glycosides were determined using high-resolution electrospray ionization mass spectrometry, nuclear magnetic resonance spectroscopy, electronic circular dichroism calculations, and chemical hydrolysis methods. The anti-inflammatory activities of the isolated compounds were evaluated by down-regulating interleukin-6 (IL-6) in lipopolysaccharide-stimulated RAW 264.7 macrophages. Notably, all the new compounds significantly inhibited the expression of IL-6 in a dose-dependent manner.


Artemisia annua , Artemisia , Sesquiterpenes , Artemisia annua/chemistry , Glycosides/pharmacology , Monoterpenes/pharmacology , Interleukin-6 , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/chemistry , Water , Sesquiterpenes/pharmacology , Artemisia/chemistry
2.
Comb Chem High Throughput Screen ; 23(9): 955-971, 2020.
Article En | MEDLINE | ID: mdl-32407262

BACKGROUND AND OBJECTIVE: Mycoplasmal pneumonia (MP) can lead to inflammation, multiple system immune damage, and mixed infection in children. The pathogenesis is still unclear. Shuang-Huang-Lian (SHL) oral liquid can treat acute upper respiratory tract infection, acute bronchitis and light pneumonia. However, our current understanding of the molecular mechanisms supporting its clinical application still lags behind due to the lack of researches. It is difficult to understand the overall sensitization mechanism of SHL oral liquid. The purpose is to explain the mechanism of action of drugs in this study, which is useful to ensure the safety of medication for children. METHODS: The therapeutic mechanism of SHL oral liquid was investigated by a system pharmacology approach integrating drug-likeness evaluation, oral bioavailability prediction, ADMET, protein-protein interaction worknet, Gene Ontology enrichment analysis, Kyoto Encyclopedia of Genes and Genomes database pathway performance, C-T-P network construction and molecular docking. RESULTS: A total of 18 active ingredients contained in SHL oral liquid and 53 major proteins were screened out as effective players in the treatment of M. pneumoniae disease through some related pathways and molecular docking. The majority of targets, hubs and pathways were highly related to anti-mycoplasma therapy, immunity and inflammation process. CONCLUSION: This study shows that the anti-bacterial effect of SHL oral liquid has multicomponent, multi-target and multi-pathway phenomena. The proposed approach may provide a feasible tool to clarify the mechanism of traditional Chinese medicines and further develop their therapeutic potentials.


Anti-Infective Agents/chemistry , Drugs, Chinese Herbal/chemistry , Pneumonia, Mycoplasma/drug therapy , Respiratory Tract Infections/drug therapy , Small Molecule Libraries/chemistry , Anti-Infective Agents/pharmacokinetics , Databases, Genetic , Drug Evaluation, Preclinical , Drugs, Chinese Herbal/pharmacokinetics , Gene Expression Regulation/drug effects , Gene Ontology , Humans , Medicine, Chinese Traditional , Molecular Docking Simulation , Protein Binding , Signal Transduction , Small Molecule Libraries/pharmacology
3.
Comb Chem High Throughput Screen ; 22(9): 612-624, 2019.
Article En | MEDLINE | ID: mdl-31694519

BACKGROUND AND OBJECTIVE: A large number of people are facing the danger of fatigue due to the fast-paced lifestyle. Fatigue is common in some diseases, such as cancer. The mechanism of fatigue is not definite. Traditional Chinese medicine is often used for fatigue, but the potential mechanism of Polygonati Rhizoma (PR) is still not clear. This study attempts to explore the potential anti-fatigue mechanism of Polygonati Rhizoma through virtual screening based on network pharmacology. METHODS: The candidate compounds of PR and the known targets of fatigue are obtained from multiple professional databases. PharmMapper Server is designed to identify potential targets for the candidate compounds. We developed a Herbal medicine-Compound-Disease-Target network and analyzed the interactions. Protein-protein interaction network is developed through the Cytoscape software and analyzed by topological methods. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment are carried out by DAVID Database. Finally, we develop Compound-Target-Pathway network to illustrate the anti-fatigue mechanism of PR. RESULTS: This approach identified 12 active compounds and 156 candidate targets of PR. The top 10 annotation terms for GO and KEGG were obtained by enrichment analysis with 35 key targets. The interaction between E2F1 and PI3K-AKT plays a vital role in the anti-fatigue effect of PR due to this study. CONCLUSION: This study demonstrates that PR has multi-component, multi-target and multipathway effects.


Drugs, Chinese Herbal/therapeutic use , Fatigue/drug therapy , Rhizome/chemistry , Drug Evaluation, Preclinical , Drugs, Chinese Herbal/chemistry , Drugs, Chinese Herbal/isolation & purification , Gene Ontology , High-Throughput Screening Assays , Humans , Medicine, Chinese Traditional , Molecular Structure , Protein Interaction Maps , Software
...