ZHOUYao, GAOKun, XIAPing, LIWei, ZHOUZhan-wei, WANGMin-jie, SUNWei, WANGLi-jun, HEWei-ming. Sulfotanshinone ⅡA Sodium Ameliorates Lipopolysaccharide-Peritoneal Dialysis Solution-Elicited Human Peritoneal Mesothelial Cells Injury[J]. Journal of Nanjing University of traditional Chinese Medicine, 2017, 33(6): 603-607.
Citation: ZHOUYao, GAOKun, XIAPing, LIWei, ZHOUZhan-wei, WANGMin-jie, SUNWei, WANGLi-jun, HEWei-ming. Sulfotanshinone ⅡA Sodium Ameliorates Lipopolysaccharide-Peritoneal Dialysis Solution-Elicited Human Peritoneal Mesothelial Cells Injury[J]. Journal of Nanjing University of traditional Chinese Medicine, 2017, 33(6): 603-607.

Sulfotanshinone ⅡA Sodium Ameliorates Lipopolysaccharide-Peritoneal Dialysis Solution-Elicited Human Peritoneal Mesothelial Cells Injury

  • OBJECTIVE To study the effect and mechanism of sulfotanshinone ⅡA sodium (STS) in human peritoneal mesothelial cells (HPMCs) injury and peritoneal fibrosis caused by lipopolysaccharide-peritoneal dialysis solution (LPS-PDS). METHODS HPMCs was primary cultured from patients undergoing peritoneal surgery. The cells were incubated with LPS-PDS to mimic the peritoneal dialysis conditions in vitro. After treatment of cells with STS, cellular viability was tested and mRNA were collected and subjected to RT-PCR to evaluated the level of TGF-β1, TIMP-1 and MMP-9. RESULTS Incubation HPMCs with LPS-PDS elicited cell injury. STS attenuated LPS-PDS-induced cell injury by improvement of cellular viability. Furthermore, STS inhibited HPMCs fibrosis as evidenced by suppression of TGF-β1 and TIMP1 induced by LPS-PDS and increasing MMP-9 mRNA level. CONCLUSION STS protects HPMCs against LPS-PDS-induced cell injury. Moreover, STS retards HPMCs fibrosis by decreasing TGF-β1 and TIMP1 mRNA level and increasing MMP-9 mRNA.
  • loading

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return