Ling-Gui-Zhu-Gan decoction inhibits cardiomyocyte pyroptosis via the NLRP3/Caspase-1 signaling pathway

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-10-20 DOI:10.1016/j.tice.2024.102588
Xiao-ni Zhao , Hui-min Ding , Yao-yao Ma , Liang Wang , Peng Zhou
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Abstract

Objective

The objective of this study was to investigate the protective mechanism of Ling-Gui-Zhu-Gan decoction (LGZGD) against LPS-ATP-induced pyroptosis in H9c2 cells.

Methods

LPS and ATP were used to induce pyroptosis in the H9c2 cell, and the cells were divided into the control, model and LGZGD groups. LDH level was detected using a colorimetric assay. ELISA was used to detect the expressions of IL-1β. Flow cytometry was utilized to observe apoptosis, while Hoechst/PI staining was used to detect pyroptosis. Immunofluorescence was employed to observe the expression levels of NLRP3 in cardiomyocytes, and RT-PCR was used to detect NLRP3, Caspase-1, GSDMD, and ASC mRNA expression. The cells were separated into seven groups: control, model, LGZGD, MCC950, LGZGD+MCC950, Nigericin and LGZGD+Nigericin. The mRNA and protein expressions were determined by RT-PCR and Western blot.

Results

LPS (10 μg/mL) for 12 h and ATP (8 mM) for 2 h were used as modeling condition. LGZGD demonstrated a significant reduction in LDH, and IL-1β levels (P<0.05, P<0.01). LGZGD dramatically reduced apoptosis rate, inhibited pyroptosis, decreased the fluorescence expressions of NLRP3, and reduced the mRNA expressions of NLRP3, ASC, Caspase-1, and GSDMD (P<0.01). Further mechanism studies showed that NLRP3, ASC, Caspase-1, and GSDMD decreased significantly when combined with NLRP3 inhibitor MCC950. Furthermore, LGZGD was able to effectively reverse the upregulation of protein and gene expression of Nigericin group (P<0.01).

Conclusion

LGZGD inhibits LPS-ATP-induced pyroptosis in H9c2 cell via the NLRP3/Caspase-1 signaling pathway.
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苓桂术甘汤通过NLRP3/Caspase-1信号通路抑制心肌细胞脓毒症。
研究目的本研究旨在探讨灵桂术甘汤(LGZGD)对LPS-ATP诱导的H9c2细胞脓毒症的保护机制:方法:用LPS和ATP诱导H9c2细胞发生热休克,将细胞分为对照组、模型组和LGZGD组。用比色法检测 LDH 水平。用 ELISA 检测 IL-1β 的表达。流式细胞术用于观察细胞凋亡,Hoechst/PI 染色用于检测细胞凋亡。免疫荧光技术用于观察心肌细胞中 NLRP3 的表达水平,RT-PCR 技术用于检测 NLRP3、Caspase-1、GSDMD 和 ASC mRNA 的表达。将细胞分为七组:对照组、模型组、LGZGD组、MCC950组、LGZGD+MCC950组、尼格瑞辛组和LGZGD+尼格瑞辛组。通过 RT-PCR 和 Western 印迹检测 mRNA 和蛋白质的表达:LPS(10 μg/mL)作用12 h,ATP(8 mM)作用2 h作为模型条件。LGZGD可显著降低LDH和IL-1β水平(PConclusion:LGZGD可通过NLRP3/Caspase-1信号通路抑制LPS-ATP诱导的H9c2细胞的脓毒症。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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