1.Treatment of invasive fungal diseases in children.
Chinese Journal of Pediatrics 2013;51(4):241-245
Amphotericin B
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administration & dosage
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therapeutic use
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Antifungal Agents
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administration & dosage
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therapeutic use
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Child
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Child, Preschool
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Fluconazole
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administration & dosage
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therapeutic use
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Humans
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Mycoses
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drug therapy
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epidemiology
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prevention & control
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Practice Guidelines as Topic
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standards
2.Effects of Various Dosage and Multiple Course of Dexamethasone on Expression of WNT Signal Transduction Pathway in Lung of Premature Rats
Journal of Applied Clinical Pediatrics 2006;0(14):-
Objective To explore the effects of various dosage and multiple course of Dexamethasone(DEX) on the expressions of WNTs,?-catenin and glycogen synthase kmase-3?(GSK-3?) genes in the lung of premature rats on the 19th day of embryo.Methods Twelve pregnant SD rats were divided into 3 groups randomly:small dose DEX group,large dose DEX group and control group with 4 rats in each group.The rats in control group were injected with saline 9 g/L;rats in small dose DEX group were injected with DEX 0.4 mg/(kg?d),and the rats in large dose DEX group were injected with DEX 0.8 mg/(kg?d) after DEX was diluted to 0.5 mL with saline.On the 19th day of gestation,fetuses were surgically taken out.The reverse transcription polymerase chain reaction PCR method was used to detect expressions of WNT7b,WNT5a,WNT2,GSK-3? and ?-catenin genes mRNA.Results The expressions of WNT7b(0.55?0.19,0.64?0.54)and ?-catenin(2.03?0.58,2.40?0.89)genes mRNA in small dose DEX group and large dose DEX group were significantly higher than those of control group(WNT7b:0.18?0.10,?-catenin:1.77?0.54)(Pa
6.Studies on the flavonoids in stem of Rhododendron anthopogonoide II.
China Journal of Chinese Materia Medica 2005;30(23):1830-1833
OBJECTIVETo further investigate the flavonoids of Rhododendron anthopogonoide.
METHODThe compounds were isolated and purified by Sephadex LH-20, polyamide and silica gel column chromatography. Their chemical structures were elucidated on the basis of physicochemical properties and spectral data.
RESULTSix compounds were isolated and identified as: taxifolin (I), guaijaverin (II), reynoutrin (III), quercitrin (IV), polystachoside (V) and quercetin-4'-O-beta-D-galactoside (VI).
CONCLUSIONFor the first time, compound VI was separated from Ericaceae plant, compounds II and V were isolated from Rhododendron plant, and compounds I and II were obtained from this plant.
Flavonoids ; chemistry ; isolation & purification ; Flavonols ; chemistry ; isolation & purification ; Galactosides ; chemistry ; isolation & purification ; Plant Leaves ; chemistry ; Plant Stems ; chemistry ; Plants, Medicinal ; chemistry ; Quercetin ; analogs & derivatives ; chemistry ; isolation & purification ; Rhododendron ; chemistry
7.Chemical constituents from Morus notabilis and their cytotoxic effect.
Pan ZHEN ; Gang NI ; Xiao-guang CHEN ; Ruo-yun CHEN ; Han-ze YANG ; De-quan YU
Acta Pharmaceutica Sinica 2015;50(5):579-582
Une new flavonoids named as notabilisin K (1), together with four known compounds, morusin (2), mulberrofuran A (3), neocyclomorusin (4) and mornigrol F (5) are separated from 95% ethanol extracts of the twigs of Morus notabilis. Compounds 2-5 are separated from this plant for the first time. Notabilisin I, notabilisin J exhibits certain effect against cells of HCT-116, HepG2 and A2780 with IC50 values ranging from 1.47 μmol x L(-1) to 5.46 μmol x L(-1). Morusin exhibits strong effect against five kinds of human cancer cells (BGC823, A2780, HCT-116, HepG2 and NCI-H1650) with IC50 values ranging from 0.74 μmol x L(-1) to 1.58 μmol x L(-1).
Antineoplastic Agents, Phytogenic
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chemistry
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Benzofurans
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chemistry
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Flavonoids
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chemistry
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Hep G2 Cells
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Humans
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Inhibitory Concentration 50
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Morus
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chemistry
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Plant Extracts
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chemistry
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Terpenes
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chemistry
8.Prospect in the study of creating new drugs from Chinese herbal medicine.
Acta Academiae Medicinae Sinicae 2002;24(4):335-338
This paper concisely describes the prospect in developing new drugs from Chinese herbal medicine. The search for bioactive constituents or leading compounds from natural sources especially from Chinese herbal medicine will be proved to be one of the most effective ways by changing the traditional concept of study on natural drugs using modern ideas. It is well known that plants in China provide a fertile source of natural compounds dealt with biological and structural diversity, which is the best channel to discover bioactive and leading compounds. Many instances have showed that structural transformation and analogues synthesis of known natural compounds or drugs can provide an important way to find new leading compounds. Study of the bioactive principle of Chinese herbal medicine involves an integration of chemical study and bioassay with intensive screening. It should be emphasized that the investigation of bioactive compounds for creating new drugs is the major task of Chinese pharmaceutical industry.
Drug Design
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Drugs, Chinese Herbal
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chemistry
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Humans
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Plants, Medicinal
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chemistry
9.Effects of 1,25-Dihydroxyvitamin D_3 on Cell Proliferation,Differentiation and Expression of Vitamin D Receptor in Mouse Osteoblast
hai-yan, GU ; chan-juan, LI ; quan, WANG ; yue, WU ; xi-rong, GUO ; de-yu, ZHAO
Journal of Applied Clinical Pediatrics 2006;0(19):-
Objective To study the effect of different concentration of 1,25-dihydroxyvitamin D3[1,25(OH)2D3] on cell proliferation,differentiation and the expression of vitamin D receptor (VDR) in mouse MC3T3E1 osteoblast.Methods Osteoblast were cultured in medium with different concentrations of 1,25(OH)2D3.Incubated for 48 h,cell proliferation of osteoblast were examined by MTT reduction assay (mono-nuclear cell direc cytotoxicity assay),the osteocalcin (OC) levels in cell medium were detected by ELISA,and the expression of VDR mRNA and protein were examined by using SYBR Green real-time PCR and Western blot,respectively.Results 1.After incubation with 1,25(OH)2D3 for 48 h,the number of MC3T3E1 osteoblast was significantly less than that in control group(P0.05).3.SYBR Green real-time PCR and Western blot results showed that the expression of VDR mRNA as well as VDR protein of osteoblast in 10-8,10-9 mol/L experimental groups were significantly higher than those in control group (Pa0.05).Conclusions Cell proliferation of mouse osteoblast can be inhibited,while the cell differentiation was promoted by 1,25(OH)2D3.1,25(OH)2D3 up-regulated the expression of VDR in mouse osteoblast,which suggested that the VDR signal pathway may play some role in proliferation and differentiation of osteoblast.
10.Structure and spectral characteristics of Diels-Alder type adducts from Morus.
Sheng-Jun DAI ; Zi-Ming LU ; Ruo-Yun CHEN ; De-Quan YU
Acta Pharmaceutica Sinica 2005;40(10):876-881
Animals
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Antihypertensive Agents
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isolation & purification
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pharmacology
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Antioxidants
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isolation & purification
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pharmacology
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Antiviral Agents
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isolation & purification
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pharmacology
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Benzofurans
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chemistry
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isolation & purification
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pharmacology
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Chromones
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chemistry
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isolation & purification
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pharmacology
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Flavonoids
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chemistry
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isolation & purification
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pharmacology
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Magnetic Resonance Spectroscopy
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Mass Spectrometry
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Molecular Structure
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Morus
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chemistry
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Plants, Medicinal
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chemistry
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Resorcinols
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chemistry
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isolation & purification
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pharmacology
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Spectrum Analysis
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methods