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芯片分析揭示了活络效灵丹抗关节炎活性的分子基础。

Microarray analysis reveals the molecular basis of antiarthritic activity of huo-luo-xiao-ling dan.

机构信息

Department of Microbiology and Immunology, University of Maryland School of Medicine, HSF-1, Suite 380, 685 West Baltimore Street, Baltimore, MD 21201, USA.

出版信息

Evid Based Complement Alternat Med. 2013;2013:524746. doi: 10.1155/2013/524746. Epub 2013 Jul 30.

Abstract

Rheumatoid arthritis (RA) is a chronic inflammatory disease of autoimmune origin. Huo-luo-xiao-ling dan (HLXL) is an herbal mixture that has been used in traditional Chinese medicine over several decades to treat chronic inflammatory diseases including RA. However, the mechanism of the anti-arthritic action of this herbal remedy is poorly understood at the molecular level. In this study, we determined by microarray analysis the effects of HLXL on the global gene expression profile of the draining lymph node cells (LNC) in the rat adjuvant arthritis (AA) model of human RA. In LNC restimulated in vitro with the disease-related antigen mycobacterial heat-shock protein 65 (Bhsp65), 84 differentially expressed genes (DEG) (64 upregulated and 20 downregulated) versus 120 DEG (94 upregulated and 26 downregulated) were identified in HLXL-treated versus vehicle (Water)-treated rats, respectively, and 62 DEG (45 upregulated and 17 downregulated) were shared between the two groups. The most affected pathways in response to HLXL treatment included immune response, inflammation, cellular proliferation and apoptosis, and metabolic processes, many of which are directly relevant to arthritis pathogenesis. These results would advance our understanding of the mechanisms underlying the anti-arthritic activity of HLXL.

摘要

类风湿关节炎(RA)是一种自身免疫性的慢性炎症性疾病。 Huo-luo-xiao-ling 丹(HLXL)是一种草药混合物,已在传统中药中使用了几十年,用于治疗包括 RA 在内的慢性炎症性疾病。然而,这种草药疗法的抗关节炎作用的机制在分子水平上还了解甚少。在这项研究中,我们通过微阵列分析确定了 HLXL 对人 RA 的佐剂关节炎(AA)模型引流淋巴结细胞(LNC)的全球基因表达谱的影响。在与疾病相关的抗原分枝杆菌热休克蛋白 65(Bhsp65)体外再刺激的情况下,与Vehicle(水)处理的大鼠相比,HLXL 处理的大鼠中有 84 个差异表达基因(DEG)(64 个上调和 20 个下调),而 120 个 DEG(94 个上调和 26 个下调),两组之间有 62 个 DEG(45 个上调和 17 个下调)共享。对 HLXL 治疗反应最受影响的途径包括免疫反应、炎症、细胞增殖和凋亡以及代谢过程,其中许多与关节炎发病机制直接相关。这些结果将增进我们对 HLXL 抗关节炎活性的机制的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e60/3745855/a2759a57108f/ECAM2013-524746.001.jpg

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