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1.
Journal of Chinese Physician ; (12): 33-35, 2013.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-432917

RESUMO

Objective To study the relationships of fatty liver with the waist to hip ratio (WHR),obesity,blood glucose,blood lipid,so as to guide clinical treatment.Methods A total of 5827 persons who underwent the following examination,including liver function,kidney function,blood lipids,blood glucose,and ultrasound imaging examination were divided into fatty liver suffering group and non-fatty liver suffering group.Results The incidences of WHR,diabetes,hyperlipidemia,and hyperuricemia in the fatty liver suffering group were significantly higher than those in the non-fatty liver suffers group(t =24.6,13.2,21.9,19.6,10.3,P < 0.01).The incidence (44.3%) of fatty liver in males was significantly higher than that (31%) in females (x2 =33.6,P < 0.01).Conclusions There was obvious correction between fatty liver and abdominal obesity.Patients with fatty liver should be given early prevention in order to prevent from the occurrence of cardiovascular events and metabolic syndrome.

2.
Chinese Journal of Digestion ; (12): 523-526, 2011.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-419715

RESUMO

Objective To explore the effects of RNAi-mediated inhibitor of growth 1 (ING1)gene silencing on cell apoptosis of human gastric cancer cell line AGS.Methods After cultured,human gastric cell line AGS was divided into blank control group, negative control group (transfected with negative control siRNA sequence) and siRNA group (transfected with specific ING1 siRNA sequence).After transfection, the ING1 gene silencing effects at different time points were detected by immunofluorescence, real-time PCR and Western blot.The effects of ING1 gene silencing on apoptosis of AGS cells were evaluated by flow cytometry.ResnltsING1 expression was restricted to the AGS cytoplasm.In real time PCR testing, the ING1 gene expression in blank control group was set as 1.24 h and 40 h after transfection, the ING1 gene relative expression quantity of negative control group was 0.88±0.16 and 0.92±0.13, and that of siRNA group was 0.38±0.09 and 0.17±0.06,respectively.Compared blank control group with negative control group, P values were 0.78 and 0.82.Compared blank control group with siRNA group, both P values were 0.01.Compared negative control group with siRNA group, P value was 0.02 and 0.01.In western blot testing, the protein expression of ING1 decreased significantly after transfected for 40 h.The apoptosis rate of blank control group was 11.06% ±0.97%, and 40 h after transfection, the apoptosis rate in AGS cells of negative control group and siRNA group was 11.82 % ± 0.69 % and 6.70% ± 0.41%, respectively.Compared negative control group with siRNA group, the P value was 0.024.Compared blank control group with negative control group, the P value was 0.76.Compared negative control group with siRNA group, the P value was 0.019.ConclusionING1 plays an important role in cell apoptosis of human gastric adenocarcinoma cells, and may become a new target for gastric cancer gene therapy.

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