首页> 美国卫生研究院文献>Data in Brief >Data on Tougu Xiaotong capsules may inhibit p38 MAPK pathway-mediated inflammation in vitro
【2h】

Data on Tougu Xiaotong capsules may inhibit p38 MAPK pathway-mediated inflammation in vitro

机译:头固消痛胶囊的数据可能会抑制体外p38 MAPK途径介导的炎症

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The Tougu Xiaotong capsule (TXC) is a traditional herbal compound used to treat osteoarthritis (OA) in China. We performed fingerprint analysis with HPLC for the quality control of TXC. Its composition was identified by the comparison of the spectrogram and chromatographic peak of retention time with a reference substance. TXC was found to contain paeoniflorin, isofraxidin, ferulic acid, and rosmarinic acid. The chondrocytes were identified by immunohistochemical staining using collagen II. Chondrocytes that were positive for collagen II were stained brown in the cytoplasm. The toll-like receptor 4 (TLR4) was expressed on the chondrocyte membrane, which was observed using immunofluorescence microscopy. The nuclei were stained blue by 4′,6-diamidino-2-phenylindole (DAPI) and TLR4 was stained green. These were observed using laser scanning confocal microscopy. The successful establishment of LPS-exposed chondrocytes was confirmed using enzyme-linked immunosorbent assay (ELISA). Lipopolysaccharide (LPS) administration significantly reduced the levels of interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α), and a maximum effect was observed at 8 h. We believe that these methods will be useful in future investigations of OA. This data article is related to the research article “Tougu Xiaotong capsules may inhibit p38 MAPK pathway-mediated inflammation: and verification” [1].
机译:头骨消痛胶囊(TXC)是在中国用于治疗骨关节炎(OA)的传统草药。我们使用HPLC进行了指纹分析,以控制TXC的质量。通过比较保留时间的色谱图和色谱峰与参考物质的比较来确定其组成。发现TXC含有pa药苷,异fraxidin,阿魏酸和迷迭香酸。通过使用胶原蛋白II的免疫组织化学染色来鉴定软骨细胞。胶原II阳性的软骨细胞在细胞质中染成棕色。使用免疫荧光显微镜观察,在软骨细胞膜上表达了toll样受体4(TLR4)。细胞核用4',6-二mid基-2-苯基吲哚(DAPI)染成蓝色,TLR4染成绿色。使用激光扫描共聚焦显微镜观察到这些。使用酶联免疫吸附测定(ELISA)证实了暴露于LPS的软骨细胞的成功建立。脂多糖(LPS)的给药可显着降低白介素1β(IL-1β)和肿瘤坏死因子-α(TNF-α)的水平,并在8 h时达到最大作用。我们认为,这些方法将在以后的OA研究中有用。该数据文章与研究文章“头固消痛胶囊可能抑制p38 MAPK途径介导的炎症:和验证”有关[1]。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号