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调脂颗粒提取物及其成分对I型B类清道夫受体表达的影响

Effects of Extracts from Tiaozhi Granule and Its Components on Expression of Scavenger Receptor Class B Type I.

作者信息

Yu Xiao, Zhao Xiao-Dong, Bao Rong-Qi, Yu Jia-Yu, Zhang Guo-Xing, Chen Jing-Wei

机构信息

Laboratory of Cancer Molecular Genetics, Medical College of Soochow University, Dushu Lake Campus, 199 Ren-Ai Road, Suzhou Industrial Park, Suzhou 215123, China.

Department of Internal Medicine, The Affiliated Suzhou Chinese Traditional Medicine Hospital, Nanjing University of Chinese Medicine, 18 Yang-Su Road, Suzhou 215003, China.

出版信息

Evid Based Complement Alternat Med. 2016;2016:9238512. doi: 10.1155/2016/9238512. Epub 2016 Dec 6.

Abstract

Sera from the rats with different drug treatments (atorvastatin, Tiaozhi granule, or its extracts) were collected. LO-2 cells or HepG2 cells were pretreated with different sera as the following groups randomly: (1) blank control group, (2) positive control group (atorvastatin group), (3) Tiaozhi granule water extract groups, (4) Tiaozhi granule alcohol extract groups, and (5) alcohol extracts for each component: , L., and . LO-2 cells were cotransfected with plasmid carrying SR-BI and pRL-TK promoter genes. Promoter activity was measured by the luciferase reporter gene assay. The mRNA and protein expressions of SR-BI were examined using real-time PCR and western blot analyses. Our results show that promoter activity and mRNA and protein expression levels of the SR-BI were significantly upregulated by Tiaozhi granules alcohol or water extracts in a dose-dependent manner. alcohol extract with a high dosage could also increase SR-BI activity and expression, but not the extracts from L. and . Both Tiaozhi granule alcohol and water extracts can upregulate SR-BI gene expression. Among the components, are important for the regulatory effect coordinating with L. and .

摘要

收集经不同药物处理(阿托伐他汀、调脂颗粒或其提取物)的大鼠血清。将LO-2细胞或HepG2细胞用不同血清预处理,随机分为以下几组:(1)空白对照组,(2)阳性对照组(阿托伐他汀组),(3)调脂颗粒水提取物组,(4)调脂颗粒醇提取物组,以及(5)各成分的醇提取物组:[此处成分名称缺失]、[此处成分名称缺失]和[此处成分名称缺失]。将携带SR-BI和pRL-TK启动子基因的质粒共转染至LO-2细胞。通过荧光素酶报告基因测定法测量启动子活性。使用实时PCR和蛋白质印迹分析检测SR-BI的mRNA和蛋白质表达。我们的结果表明,调脂颗粒醇提取物或水提取物以剂量依赖性方式显著上调SR-BI的启动子活性以及mRNA和蛋白质表达水平。高剂量的[此处成分名称缺失]醇提取物也可增加SR-BI活性和表达,但[此处成分名称缺失]和[此处成分名称缺失]的提取物则无此作用。调脂颗粒醇提取物和水提取物均可上调SR-BI基因表达。在这些成分中,[此处成分名称缺失]对于与[此处成分名称缺失]和[此处成分名称缺失]协同发挥调节作用很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b050/5168482/c7f331558809/ECAM2016-9238512.001.jpg

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