中南药学2024,Vol.22Issue(6) :1571-1576.DOI:10.7539/j.issn.1672-2981.2024.06.026

羟基积雪草苷通过抑制NF-κB/NLRP3细胞焦亡通路缓解间质性膀胱炎

Madecassoside alleviates interstitial cystitis by inhibiting the pyroptosis of NF-κB/NLRP3 pathway

李琪 浦东 王思思 谢璇 李霁 于锋
中南药学2024,Vol.22Issue(6) :1571-1576.DOI:10.7539/j.issn.1672-2981.2024.06.026

羟基积雪草苷通过抑制NF-κB/NLRP3细胞焦亡通路缓解间质性膀胱炎

Madecassoside alleviates interstitial cystitis by inhibiting the pyroptosis of NF-κB/NLRP3 pathway

李琪 1浦东 1王思思 1谢璇 1李霁 1于锋1
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作者信息

  • 1. 中国药科大学基础医学与临床药学学院,南京 211198
  • 折叠

摘要

目的 通过NF-κB/NLRP3 介导的细胞焦亡途径探究羟基积雪草苷对间质性膀胱炎的相关作用.方法 通过脂多糖建立体外间质性膀胱炎细胞模型,使用不同浓度的羟基积雪草苷处理,采用MTT、单层细胞划痕伤口实验、实时荧光定量PCR和蛋白印迹实验检测羟基积雪草苷对SV-HUC-1 细胞间质性膀胱炎体外模型中细胞活力,伤口愈合能力和NF-κB/NLRP3 通路介导的细胞焦亡相关蛋白和mRNA的表达的作用.结果 体外细胞实验结果显示,与模型组相比,羟基积雪草苷能改善细胞活力和伤口愈合能力,并抑制细胞模型中NF-κB/NLRP3 通路介导的细胞焦亡相关蛋白和mRNA的表达.结论 在脂多糖诱导的SV-HUC-1 细胞间质性膀胱炎体外模型中,羟基积雪草苷可通过抑制NF-κB/NLRP3 通路介导的细胞焦亡从而发挥对膀胱上皮细胞的保护作用.

Abstract

Objective To determine the potential effect of madecassoside on interstitial cystitis(IC)through the pyroptosis mediated by NF-κB/NLRP3.Methods An in vitro IC model induced by lipopolysaccharide in SV-HUC-1 cells was used to evaluate the effect of different concentrations of madecassoside.The protective effects of madecassoside on human ureteral epithelial cells were assessed with the MTT cell viability assay and single-layer cell scratch assay.The inhibitory effects of madecassoside on NF-κB/NLRP3-mediated pyroptosis were investigated through Western blot and real-time PCR analysis.Results Madecassoside enhanced the cell viability and wound healing compared to the model group in vitro.It effectively suppressed the expression of pyroptosis-related proteins and mRNA mediated by the NF-κB/NLRP3 pathways in the cell model.Conclusion Madecassoside demonstrates a protective role in the lipopolysaccharide induced SV-HUC-1 cell model of IC by inhibiting pyroptosis through the NF-κB/NLRP3 pathways.

关键词

间质性膀胱炎/羟基积雪草苷/NF-κB/NLRP3/细胞焦亡

Key words

interstitial cystitis/madecassoside/NF-κB/NLRP3/pyroptosis

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出版年

2024
中南药学
湖南省药学会

中南药学

CSTPCD
影响因子:0.736
ISSN:1672-2981
参考文献量4
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