Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 3 de 3
Filtrer
Plus de filtres








Gamme d'année
1.
Article de Chinois | WPRIM | ID: wpr-275472

RÉSUMÉ

Five main flavonoids of Hebei Xiangju were studied using the Density Functional Theory (DFT) B3LYP method with 6-311 G (d) basis set.Their activities were analyzed based on molecular structure,bond dissociation energy (BDE),natural orbital charge distribution (NBO),bond order and the energy gap between HOMO and LUMO. The results showed that the existing of intra molecular hydrogen bond in B ring can improve the antioxidant activity of the flavonoids, at the same time, the hydroxyl groups on the glycosides do not have the activity of eliminating free radicals, but decrease the total molecular antioxidant activity. As a result, the antioxidant ability order of the five flavonoids compounds is luteolin< luteolin-7-O-glucoside< apigenin < acacetin < acacetin-7-O-glucose, which is agreement with the experimental conclusion reported in literature. The results showed that the DFT method can provide theoretical guidance for the selection of natural flavonoid antioxidants.

2.
Article de Chinois | WPRIM | ID: wpr-232797

RÉSUMÉ

<p><b>OBJECTIVE</b>To construct an eukaryotic expression plasmid containing gp120 gene of HIV-1 subtype B and obtain gp120 gene expression in HepG2 cells.</p><p><b>METHODS</b>According to the published gp120 gene sequence in Genbank, a pair of primers was designed and synthesized. The PCR amplification product of gp120 gene was cloned into pMD-18T vector using TA cloning followed by BamHI and XhoI digestion and sequence analysis. The target gene was then subcloned into a highly efficient eukaryotic expression vector pcDNA3.1 (+). The recombinant plasmid was sequenced and identified by restrictive endonuclease digestion, and transfected into HepG2 cells via liposome. The expression of gp120 gene was analyzed by RT-PCR and Western blotting, respectively.</p><p><b>RESULTS</b>Restriction endonuclease digestion and sequence analysis verified successful construction of the recombinant vector pcDNA3.1(+)/gp120. The target fragment gp120 was identical with U26942 in Genbank, and the expression of gp120 gene was detected in the lysate of the transfected HepG2 cells by RT-PCR and Western blotting.</p><p><b>CONCLUSION</b>The eukaryotic expression plasmid for gp120 has been constructed successfully, which is capable of stable expression in HepG2 cells.</p>


Sujet(s)
Humains , Vaccins contre le SIDA , Génétique , Séquence nucléotidique , Carcinome hépatocellulaire , Génétique , Métabolisme , Anatomopathologie , Lignée cellulaire tumorale , Clonage moléculaire , Cellules eucaryotes , Métabolisme , Expression des gènes , Protéine d'enveloppe gp120 du VIH , Génétique , VIH-1 (Virus de l'Immunodéficience Humaine de type 1) , Génétique , Tumeurs du foie , Génétique , Métabolisme , Anatomopathologie , Données de séquences moléculaires , Plasmides , Génétique , Transfection , Vaccins à ADN , Génétique
3.
Acta Pharmaceutica Sinica ; (12): 496-500, 2003.
Article de Chinois | WPRIM | ID: wpr-266652

RÉSUMÉ

<p><b>AIM</b>To investigate the molecular mechanisms of saponins from the rhizome of Anemarrhena asphodeloides Bunge.</p><p><b>METHODS</b>Oligonucleotide microarrays consisting of 87 probes representing 87 human cardiovascular disease-related genes were constructed. Effects of saponins on gene expression in human umbilical vein endothelial cells were analyzed by comparing hybridization of Cy 5-labeled cDNAs from saponins-treated human umbilical vein endothelial cells and Cy 3-labeled cDNAs from untreated human umbilical vein endothelial cells.</p><p><b>RESULTS</b>The results indicate that angiotensinogen gene, alpha 2A-adrenoceptor gene and endothelin-converting enzyme 1 gene were downregulated 2.8, 1.9 and 3.1 folds respectively after human umbilical vein endothelial cells were incubated in medium containing 80 mg.L-1 saponins.</p><p><b>CONCLUSION</b>These results suggest that saponins may have beneficial effect on cardiovascular diseases by modulating the function of vein endothial cells and microarray can be used to investigate the biological action of extracts from traditional Chinese medicine.</p>


Sujet(s)
Humains , Anemarrhena , Chimie , Angiotensinogène , Génétique , Métabolisme , Aspartic acid endopeptidases , Génétique , Métabolisme , Cellules cultivées , Régulation négative , Enzymes de conversion de l'endothéline , Endothélium vasculaire , Biologie cellulaire , Métabolisme , Expression des gènes , Metalloendopeptidases , Séquençage par oligonucléotides en batterie , Plantes médicinales , Chimie , Récepteurs alpha-2 adrénergiques , Génétique , Métabolisme , Rhizome , Chimie , Saponines , Pharmacologie , Veines ombilicales , Biologie cellulaire , Métabolisme
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE