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1.
Artigo em Chinês | WPRIM | ID: wpr-888119

RESUMO

The present study aimed to explore the effect of Erxian Decoction on proteomics of osteoblasts stimulated by hydrogen peroxide(H_2O_2) and its protective mechanism with the H_2O_2-induced cell model of oxidative stress. The primary osteoblasts were cultured from the skulls of newborn rats(within 24 hours) and divided into a control group, a model group, a Fosamax group, and an Erxian Decoction group. Blank serum was added in the control group and model group, and the drug-containing serum was added correspondingly to the remaining two groups. After 45 hours, H_2O_(2 )stimulation was conducted for three hours except for the control group, followed by protein extraction. Nano-LC-LTQ-Orbitrap system was used for protein detection, Protein Discovery for protein identification, and SIEVE for quantitative and qualitative analysis. Furthermore, following the blocking of PI3 K signaling pathway by LY294002(10 μmol·L~(-1)), a control group, a model group, an LY294002 group, an Erxian Decoction group, and an Erxian Decoction + LY294002 group were set up to observe the effect of Erxian Decoction on cell proliferation, alkaline phosphatase(ALP) activity, and the relative expression of BMP-2, OPG, p-Akt, p-FoxO1 of osteoblasts stimulated by H_2O_2 under LY294002 intervention. The results revealed that 78 differential proteins were discovered between the Erxian Decoction group and model group, which were involved in the regulation of PI3 K/Akt, glucagon, estrogen, insulin, and other signaling pathways. LY294002 blunted the promoting effect of Erxian Decoction on osteoblast proliferation and significantly down-regulated the expression of OPG and p-FoxO1, whereas its down-regulation on the expression of BMP-2 and p-Akt was not significant. Both LY294002 and Erxian Decoction increased the ALP activity of osteoblasts, which may be related to the cell state and the cell differentiation. The above results suggest that Erxian Decoction can protect osteoblasts stimulated by H_2O_2, with the PI3 K/Akt signaling pathway as one of the internal mechanisms.


Assuntos
Animais , Ratos , Medicamentos de Ervas Chinesas , Peróxido de Hidrogênio , Osteoblastos/metabolismo , Fosfatidilinositol 3-Quinases/metabolismo , Proteômica , Proteínas Proto-Oncogênicas c-akt/metabolismo , Transdução de Sinais
2.
Artigo em Chinês | WPRIM | ID: wpr-293653

RESUMO

<p><b>OBJECTIVE</b>To observe the clinical effect of Xiao Gu San on cirrhosis ascites.</p><p><b>METHOD</b>Groups were randomly divided into treating group and group of western medicine comparision.</p><p><b>RESULT</b>30 cases of the treating group were observed with the following result: first class curative effect 7; second class 12; the third class 9; effectiveless 2; total effective rate 93.33%. 30 cases of the Group of Comparison: first class curative effect 2; second class 6; the third class 15; effectiveless 7; total effective rate is 76.67%.</p><p><b>CONCLUSION</b>The curative effect of Xiaogu San combined with Western medicine on cirrhosis ascites is better than that of Western medicine alone.</p>


Assuntos
Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Alanina Transaminase , Metabolismo , Ascite , Sangue , Tratamento Farmacológico , Aspartato Aminotransferases , Metabolismo , Quimioterapia Combinada , Medicamentos de Ervas Chinesas , Usos Terapêuticos , Cirrose Hepática , Sangue , Tratamento Farmacológico , Resultado do Tratamento
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