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Global Protein Expression Analysis of Molecular Markers of DS-1-47,a Component of Implantation-promoting Traditional Chinese Medicine 被引量:3
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作者 Yan-ling LI Xiao-yan ZHANG +3 位作者 Yu LENG Yan-li WU Jing LI Yun-xia WU 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2016年第6期910-915,共6页
This study investigated the molecular markers of DS-1-47,a component of an implantation-promoting traditional Chinese medicine consisting of Astragalus mongholicus,Atractylodes macrocephala,Scutellaria baicalensis and... This study investigated the molecular markers of DS-1-47,a component of an implantation-promoting traditional Chinese medicine consisting of Astragalus mongholicus,Atractylodes macrocephala,Scutellaria baicalensis and Dipsacales,in an attempt to clarify the molecular mechanism and action targets of DS-1-47.Controlled ovarian stimulation(COS) method was used to establish the implantation dysfunction models of mice.Animals were divided into normal pregnant group,COS model group and DS-1-47 group.Laser capture microdissection-double dimensional electrophoresis-mass spectrum(LCM-DE-MS) was used to analyze the uterine protein molecules that were possibly involved in the promotion of implantation.Twenty-three proteins in DS-1-47 group were significantly changed as compared to those in COS model group,with 7 proteins down-regulated and 16 proteins up-regulated.Except for some constituent proteins,the down-regulated proteins included collagen α-1(Ⅵ) chain,keratin 7,keratin 14,myosin regulatory light chain 12 B,myosin light polypeptide 9,heat shock protein β-7,and C-U-editing enzyme APOBEC-2;the up-regulated proteins included apolipoprotein A-I,calcium regulated protein-3,proliferating cell nuclear antigen,L-xylulose reductase,and calcium binding protein.These 23 proteins that were regulated by DS-1-47 represented a broad diversity of molecule functions.The down-regulated proteins were associated with stress and immune response,and those up-regulated proteins were related to proliferation.It was suggested that these proteins were important in regulating the uterine environment for the blastocyst implantation.By identification of DS-1-47 markers,proteomic analysis coupled with functional assays is demonstrated to be a promising approach to better understand the molecular mechanism of traditional Chinese medicine. 展开更多
关键词 DS-1-47 promoting implantation PROTEOMICS lcm-de-ms
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DS-1-47促着床的靶点分子筛选研究
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作者 章晓燕 李彦玲 +1 位作者 吴艳丽 吴云霞 《中西医结合研究》 2017年第3期126-131,共6页
目的研究筛选DS-1-47促着床的分子靶点。方法采用皮下注射吲哚美辛的方法建立胚泡着床障碍动物模型,动物随机分为正常组(N)、模型组(M)和中药组(Z),运用蛋白组学激光捕获显微切割技术-二维电泳-质谱(LCM-DE-MS)的技术路线研究分析DS-1-4... 目的研究筛选DS-1-47促着床的分子靶点。方法采用皮下注射吲哚美辛的方法建立胚泡着床障碍动物模型,动物随机分为正常组(N)、模型组(M)和中药组(Z),运用蛋白组学激光捕获显微切割技术-二维电泳-质谱(LCM-DE-MS)的技术路线研究分析DS-1-47作用前后子宫组织中蛋白分子的变化,筛选得到DS-1-47促进着床的关键分子,从而深入阐明其发挥作用的分子机制。结果 Z组能使11种蛋白质的表达发生明显改变,其中3种蛋白质的表达M组较N组明显下调,Z组较M组明显上调,这3种蛋白质经鉴定分别为肝羧酸酯酶、丝氨酸蛋白酶抑制剂、载脂蛋白A-Ⅰ;另外8种蛋白质的表达M组较N组明显上调,Z组较M组明显下调,蛋白质分别为血液结合素、激肽原-1、丝氨酸蛋白酶抑制剂A3K、α-1-抗胰蛋白酶1-3、结合珠蛋白、延伸因子-1-Δ、膜联蛋白A5、血清淀粉样蛋白P成分。结论血液结合素、结合珠蛋白、载脂蛋白A-Ⅰ、膜联蛋白A5、激肽原-1、延伸因子-1-Δ、丝氨酸蛋白酶抑制剂等可能是复方DS-1-47促进着床的重要靶点。 展开更多
关键词 DS-1-47 着床 蛋白质组学 激光捕获显微切割技术-二维电泳-质谱
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