4.7 Article

Artesunate inhibits fibroblasts proliferation and reduces surgery-induced epidural fibrosis via the autophagy-mediated p53/p21waf1/cip1 pathway

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 842, Issue -, Pages 197-207

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2018.10.048

Keywords

Artesunate (ART); Fibroblast proliferation; Fibroblast autophagy; Epidural fibrosis; p53/p21(waf1/cip1) pathway

Funding

  1. National Natural Science Foundation of China [81772332, 81772331]
  2. Jiangsu Provincial Medical Innovation Team [CXTDB2017004]
  3. Jiangsu Provincial Medical Youth Talent [QNRC2016343, QNRC2016344]

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Fibroblast proliferation is considered to be a major cause in the process of epidural fibrosis formation. Autophagy is a tightly-regulated catabolic process in charge of degrading intracellular components. Although autophagy has been associated with fibrosis of different tissues, the effect of autophagy on epidural fibrosis is still unknown. The aim of this study was to investigate the function and mechanism of autophagy induced by Artesunate (ART), a classical antimalarial agent extracted from the Chinese medicinal herb. In vitro, the effect of ART on inducing fibroblast autophagy was evaluated via LC3 immunofluorescent staining, Transmission Electron Microscopy (TEM) and western blotting analysis. Moreover, the effect of ART on inhibiting fibroblast proliferation was investigated by CCK-8 assay, EdU incorporation assay, flow cytometry and western blotting analysis. Results indicated that ART could induce autophagy and inhibit proliferation in fibroblasts. The inhibitory effect of ART on fibroblast proliferation was associated with the upregulation of and p53/p21(waf1/cip1) proteins. Intriguingly, 3-MA, a classical autophagy inhibitor, attenuated ART-induced p53/p21(waf1/cip1) pathway activation and fibroblast proliferation inhibition. In vivo, the effect of ART on reducing epidural fibrosis was detected by histological macroscopic assessment, hydroxyproline content analysis, histological and immunohistochemical staining. The results revealed that ART had significant suppressive effects on epidural fibrosis following laminectomy in rats. In conclusion, this research demonstrated that ART could inhibit fibroblast proliferation and reduce epidural fibrosis formation after laminectomy, and the potential mechanism might through autophagy cascade-mediated p53/p21(waf1/cip1) pathway. It might provide a novel reagent for reducing epidural fibrosis after spinal laminectomy surgery.

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