Ginsenoside Rk2 Protects against Ulcerative Colitis via Inactivating ERK/MEK Pathway by SIRT1

被引:3
|
作者
Huang, Xiaodong [1 ]
Xiao, Jianwei [2 ]
Wen, Mudan [3 ]
Liang, Jinghua [4 ]
机构
[1] Shenzhen TCM Anorectal Hosp Futian, Dept Surg 3, Shenzhen, Peoples R China
[2] Shenzhen Futian Hosp Rheumat Dis, Dept Rheumatol & Immunol, Shenzhen, Peoples R China
[3] Peoples Hosp Longhua, Obstet Dept, Shenzhen, Peoples R China
[4] Shenzhen TCM Anorectal Hosp Futian, 1 Songling Rd, Shenzhen 518031, Peoples R China
关键词
ulcerative colitis; Ginsenoside Rk2; inflammation; ERK; MEK; SIRT1; PANAX-GINSENG; PHARMACOLOGY; COMPONENTS; CELLS;
D O I
暂无
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Background: Chinese traditional medicine is widely used in the treatment of ulcerative colitis (UC). Ginsenoside Rk2 is a newly discovered dammarane triterpenoid saponin isolated from ginseng. Our study aimed to investigate the effects of Ginsenoside Rk2 on UC. Methods: Human clones of colorectal adenocarcinoma Caco-2 cells and human intestinal epithelial HIP-1 cells were co-cultured to establish a UC model in vitro. Cell viability and apoptosis were analyzed by cell counting kit 8 (CCK-8) and flow cytometry assay, respectively. Inflammatory cytokines' mRNA levels were measured by real-time quantitative polymerase chain reaction (RT-qPCR). Western blot was applied to examine the protein expression of apoptosis-associated proteins and the activation of the extracellular signal-regulated kinase (ERK)/mitogen-activated protein kinase (MEK) pathway. Furthermore, fisetin, an ERIC kinase activator, was used to carry out rescue experiment. SRT1720, an activator of SIRTI, was applied to increase the SIRTI protein levels while SIRTI inhibitor nicotinamide (NAM) exerted the opposite effect. Results: Ginsenoside Rk2 promoted cell viability, suppressed cell apoptosis, and reduced the release of pro-inflammatory cytokines including interleukin (IL)-1 beta, IL-6, IL-10, and tumor necrosis factor-alpha (TNF-alpha) of HT-29 cells in UC model in a concentration-dependent manner. Meanwhile, the inhibitory effects of Ginsenoside Rk2 on the ERK/MEK pathway strengthened with the increase of concentration, and was verified by fisetin application. Furthermore, the upregulation of SIRT1 induced by Ginsenoside Rk2 prompted dephosphorylation of ERK and MEK to attenuate ERK/MEK pathway activation and reduced inflammatory progress, which was confirmed by SRT1720 as well as NAM. Conclusions: Ginsenoside Rk2 inactivated ERK/MEK pathway by regulating SIRT1 to restore the cellular function of human intestinal epithelial THP-1 cells. Therefore, Ginsenoside Rk2 may be effective in the treatment of UC.
引用
收藏
页码:89 / 98
页数:10
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