首页> 外文期刊>European Journal of Pharmacology: An International Journal >Artesunate inhibits fibroblasts proliferation and reduces surgery-induced epidural fibrosis via the autophagy-mediated p53/p21(waf1/cip1) pathway
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Artesunate inhibits fibroblasts proliferation and reduces surgery-induced epidural fibrosis via the autophagy-mediated p53/p21(waf1/cip1) pathway

机译:青蒿琥酯抑制成纤维细胞增殖,通过自噬介导的P53 / P21(WAF1 / CIP1)途径降低了手术诱导的硬膜外纤维化

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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.
机译:成纤维细胞增殖被认为是硬膜外纤维化形成过程中的主要原因。自噬是一种紧压的分解代谢过程,负责降解细胞内部件。虽然自噬与不同组织的纤维化有关,但自噬对硬膜外纤维化的效果仍然未知。本研究的目的是探讨艺术品(ART)诱导的自噬的功能和机制,一种从中药草药中提取的古典抗疟剂。在体外,通过LC3免疫荧光染色,透射电子显微镜(TEM)和Western印迹分析评估了术语对诱导成纤维细胞自噬的效果。此外,通过CCK-8测定,EDU掺入测定,流式细胞术和Western印迹分析研究了艺术对抑制成纤维细胞增殖的影响。结果表明,艺术可以诱导自噬和抑制成纤维细胞的增殖。技术抑制作用对成纤维细胞增殖的抑制作用与P53 / P21(WAF1 / CIP1)蛋白的上调相关。有趣的,3- mA,古典自噬抑制剂,减毒诱导的P53 / P21(WAF1 / CIP1)途径活化和成纤维细胞增殖抑制。在体内,通过组织学宏观评估,羟脯氨酸含量分析,组织学和免疫组织化学染色来检测艺术艺术对减少硬膜外纤维化的影响。结果表明,在大鼠椎板切除术后,艺术对硬膜外纤维化具有显着的抑制作用。总之,本研究表明,艺术术后抑制成纤维细胞增殖并降低椎板切除术后硬膜外纤维化形成,潜在机制可以通过自噬级联介导的P53 / P21(WAF1 / CIP1)途径。它可能提供一种新型试剂,用于降低脊髓椎板切割术后硬膜外纤维化。

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