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삼백초(三白草)의 소염작용(消炎作用)에 대(對)한 실험적(實驗的) 연구(硏究)
변형국 ( Hyung Kuk Byun ),신용완 ( Yong Wan Shin ),김의일 ( Eui Il Kim ),김수민 ( Su Min Kim ),이정은 ( Jung Eun Lee ),유동열 ( Dong Youl Yoo ) 대한한방부인과학회 2005 大韓韓方婦人科學會誌 Vol.18 No.4
Purpose: The purpose of this research was to investigate the effects of Saurui Herba Seu Rhizoma(SHSR) on Anti-inflammatory properties in Raw264.7 cell line and murine models of inflammation. Methods: To investigate the effects of Saurui Herba Seu Rhizoma(SHSR) on anti-inflammation, we study cytotoxicity effects of SHSR on Mouse Lung Fibroblast Cells and Peritoneal Macrophages, Inhibitory effects of SHSR on the nitric oxide (NO) release, the ROS production, and the interleukin-6 production. Results: The cytotoxicity of SHSR on mouse lung fibroblast Cells and Raw264.7 cell line was not observed. SHSR in RAW264.7 cell line inhibited IL-1β, IL-6 mRNA gene expression depending upon the concentrations of extract and inhibited IL-18 mRNA gene expression at 100 ㎍/㎖ of extract. SHSR in RAW264.7 cell line inhibit COX-2 mRNA gene expression at 100, 10 ㎍/㎖ of extract. SHSR in RAW264.7 cell line inhibited NOS-Ⅱ mRNA gene expression depending upon the concentrations of extract. SHSR in RAW264.7 cell line didn``t inhibit TNF-α mRNA gene expression. SHSR in RAW264.7 cell line decreased IL-6 production depending upon the concentrations of extract. SHSR in RAW264.7 cell line decreased ITNF-α production according to the concentrations of extract. SHSR in RAW264.7 cell line inhibited NO release specially SHSR 100, 10 ㎍/㎖ concentrations of extract. SHSR inhibit ROS production depending upon the concentrations of extract. Conclusion: These results suggest that SHSR can be used treating a lot of women disease caused by inflammation.
우슬산(牛膝散)의 항혈전작용(抗血栓作用)에 대(對)한 실험적(實驗的) 연구(硏究)
김경수 ( Kyung Su Kim ),신용완 ( Yong Wan Shin ),김의일 ( Eui Il Kim ),김수민 ( Su Min Kim ),이정은 ( Jung Eun Lee ),유동열 ( Dong Youl Yoo ) 대한한방부인과학회 2005 大韓韓方婦人科學會誌 Vol.18 No.3
Purpose: The Purpose of this research was to investigate the effects of antithrombotic activities of Wuslsan (WSS). Methods: Measure the effect which was given to blood flow rate through the regular volume of glass tube after the blood was diluted five times with ACD soulution. Antithrombotic effect was calculated as a percentage of the experimental animal figure protected from the paralysis of hind legs or death of the mouse that is caused from the administration of platelet aggregation regent. Being classified one group of eight mice, each of them was divided into Normal, Control, and WSS. The normal group supplied a saline solution and the control group brought the dextran extravasated blood after an hour of administering the saline solution. Also WSS was dissolved in 2㎖ saline solution and then we dosed it to the experimental mice with Oral Zonde one day before the experiment. After that, the mice were abstained from food. And then we gave a measured amount of it before an hour. Finally, it gave rise to dextran extravasated blood in the same way as the Control group. Results: The results were obtained as follows. WSS inhibited platelet aggregation induced by ADP and epinephrine significantly as compared with the control group. WSS showed fibrinolytic activity insignificantly as compared with the control group. WSS increased blood flow rate significantly as compared with the control group in vitro. WSS inhibited pulmonary embolism induced by collagen and Epinephrine (inhibitive rate is 37.5%). WSS increased number of platelet and fibrinogen amount significantly, and shortened PT and APTT as compared with the control group in thrombus model induced by dextran. Conclusion: WSS is effective antithrombotic activity from experimental result.