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1.
China Journal of Chinese Materia Medica ; (24): 1334-1341, 2015.
Artículo en Chino | WPRIM | ID: wpr-246099

RESUMEN

<p><b>OBJECTIVE</b>The multiple levels fragmentations of five furocoumarine (psoralen, xanthotoxin, bergapten, oxypeucedanin, and byakangelicol) in Angelica dahurica have been demonstrated using LTQ-Orbitrap mass spectrometry with high resolution and high mass accuracy to discover the possible,fragmentation regularity.</p><p><b>METHOD</b>Duringcollsion-induced dissociation (CID), the MS(n) data of the five compoundswhich were gained in the positive ion mode at 35ev collision energy by direct injection syrings method were analyzed using Xcalibar 2.0 Software to infer the formula of these fragmentations.</p><p><b>RESULT</b>The results indicated that the five compounds have similar fragmentation process with CO meutral lost at C5,C8-subsituents and furan ring, meanwhile the meutralloss of CO2 occurred easily at lactone group.</p><p><b>CONCLUSION</b>This method is helpful in identifying the structures of other furocoumarinein Angelica dahuricaand their metabolites in vivo.</p>


Asunto(s)
Angelica , Química , Fenómenos Químicos , Cumarinas , Química , Medicamentos Herbarios Chinos , Química , Espectrometría de Masas , Métodos , Estructura Molecular
2.
Chinese Journal of Epidemiology ; (12): 920-924, 2010.
Artículo en Chino | WPRIM | ID: wpr-277760

RESUMEN

Objective To detect thc distribution ofpolymorphism of GSTP1 and infection rate of Helicobacter pylori (H. Pylori) in different kinds of gastric intestinal metaplasia (IM) and to explore the relationship between entergenic factor-polymorphism of GSTP1 and extogenic factor-H, pylori infection, to determine thc risk of subtype of IM. Methods There were 381 cases in total, including 143 CGS( + ) and 238 IM. H. E. Stain was used for pathological diagnosis. HID-AB-pH2.5 methods were used to classify the IM. ELISA method was used to detect the antibody of H. Pylor-IgG.Polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) were used to analyze the genotype. Results Frequency of G genotype was higher in the IM group, when compared to the CGS ( + ) groups (P<0.05). The positive rate of H. Pyloriwas statistically higher than CGS( + )(P<0.01 ). By effect-modified model analysis, GSTP1 gene polymorphsim and H. Pyloriinfection presented a positive interaction in the stage IM,with the OR value as 9.386 (95%CI:3.736-23.580) after adjusted by age and gender. The synergy index was 2.078 and the attributable proportion of interaction was 46.36%. The positive rate of H. Pyloriwere statistically bighter than CGS ( + ) group in subtype IM Ⅰ , subtype IM Ⅱ and Ⅲ (P<0.01). The frequency of G genotype was higher in the IM Ⅱ and Ⅲ group, when compared with the IM Ⅰ groups (P<0.01). By effectmodified model analysis, in the stage of IM Ⅱ and Ⅲ, GSTP1 gene polymorphsim and H. Pylori infection also presented a positive interaction, with OR value as 24.487 (95%CI: 7.731-77.735 )after adjusted by age and gender, with its synergy index as 1.844, and attributable proportion of interaction as 43.89%. Conclusion The infection of H.pyloriand polymorphism GSTP1 gene appeared to be both the external and internal factors, respectively. In the stage of IM, GSTP1 gene polymorphsim and H. Pylori infection also presented a positive interaction, expecially in the IM Ⅱ and Ⅲ.

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