Ethyl Lithospermate Reduces Lipopolysaccharide-Induced Inflammation through Inhibiting NF-κB and STAT3 Pathways in RAW 264.7 Cells and Zebrafish

被引:1
|
作者
Zhou Chun-hong [1 ,2 ]
Yang Hua [1 ,2 ]
Zou Li-fang [1 ,2 ]
Liu Di-fa [3 ]
Yu Lin-zhong [1 ,2 ]
Cao Hui-hui [1 ,2 ]
Deng Li-e [4 ]
Wang Zhang-wei [3 ]
Lu Zi-bin [1 ,2 ]
Liu Jun-shan [1 ,2 ]
机构
[1] Southern Med Univ, Level Res Lab State Adm Tradit Chinese Med 3, Guangdong Prov Key Lab Chinese Med Pharmaceut, Sch Tradit Chinese Med, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Zhujiang Hosp, Dept Pharm, Guangzhou 510282, Peoples R China
[3] Jiangxi Qingfeng Pharmaceut Co Ltd, State Key Lab Innovat Nat Med & Tradit Chinese Me, Ganzhou 341000, Jiangxi, Peoples R China
[4] Southern Med Univ, Affiliated Dongguan Peoples Hosp, Dongguan 523076, Guangdong, Peoples R China
关键词
ethyl lithospermate; anti-inflammation; nuclear factor kappa B; signal transducer and activator of transcription 3; lipopolysaccharide; zebrafish; TRANSCRIPTION; IMMUNITY; DANSHEN;
D O I
10.1007/s11655-023-3643-y
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
ObjectiveTo explore the anti-inflammatory effects of ethyl lithospermate in lipopolysaccharide (LPS)-stimulated RAW 264.7 murine-derived macrophages and zebrafish, and its underlying mechanisms.Methods3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazoliumbromide (MTT) assays were performed to investigate the toxicity of ethyl lithospermate at different concentrations (12.5-100 mu mol/L) in RAW 264.7 cells. The cells were stimulated with LPS (100 ng/mL) for 12 h to establish an inflammation model in vitro, the production of pro-inflammatory cytokines interleukin (IL)-6 and tumor necrosis factor alpha (TNF-alpha) were assessed by enzyme linked immunosorbent assay (ELISA). Western blot was used to ascertain the protein expressions of signal transducer and activator of transcription 3 (STAT3), nuclear factor kappa B (NF-kappa B) p65, phospho-STAT3 (p-STAT3, Tyr705), inhibitor of NF-kappa B (I kappa B) alpha, and phospho-I kappa B alpha (p-I kappa B alpha, Ser32), and confocal imaging was used to identify the nuclear translocation of NF-kappa B p65 and p-STAT3 (Tyr705). Additionally, the yolk sacs of zebrafish (3 days post fertilization) were injected with 2 nL LPS (0.5 mg/mL) to induce an inflammation model in vivo. Survival analysis, hematoxylin-eosin (HE) staining, observation of neutrophil migration, and quantitative real-time polymerase chain reaction (qRT-PCR) were used to further study the anti-inflammatory effects of ethyl lithospermate and its probable mechanisms in vivo.ResultsThe non-toxic concentrations of ethyl lithospermate have been found to range from 12.5 to 100 mu mol/L. Ethyl lithospermate inhibited the release of IL-6 and TNF-alpha(P<0.05 or P<0.01), decreased I kappa B alpha degradation and phosphorylation (P<0.05) as well as the nuclear translocation of NF-kappa B p65 and p-STAT3 (Tyr705) in LPS-induced RAW 264.7 cells (P<0.01). Ethyl lithospermate also decreased inflammatory cells infiltration and neutrophil migration while increasing the survival rate of LPS-stimulated zebrafish (P<0.05 or P<0.01). In addition, ethyl lithospermate also inhibited the mRNA expression levels of of IL-6, TNF-alpha, I kappa B alpha, STAT3, and NF-kappa B in LPS-stimulated zebrafish (P<0.01).ConclusionEthyl lithospermate exerts anti-Inflammatory effected by inhibiting the NF-kappa B and STAT3 signal pathways in RAW 264.7 macrophages and zebrafish.
引用
收藏
页码:1111 / 1120
页数:10
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