Effects of penehyclidine hydrochloride on myocardial ischaemia-reperfusion injury in rats by inhibiting TLR4/MyD88/NF-κB pathway via miR-199a-3p.

IF 1.8 4区 生物学 Q4 CELL BIOLOGY
Ling Qiang Bai, Bin Zhe Wang, Qi Wei Liu, Wen Qiang Li, Hang Zhou, Xiao Yan Yang
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引用次数: 1

Abstract

This study was to probe the role of penehyclidine hydrochloride (PHC) mediating the impact of toll-like receptor 4 (TLR4)/myeloid differentiation factor 88 (MyD88)/nuclear factor-kappa B (NF-κB) signalling pathway on myocardial ischaemia-reperfusion injury (MI/RI) in rats through miR-199a-3p. The rat MI/RI model was established through ligating left anterior descending (LAD) coronary artery. PHC was injected preoperatively into the model rats, and injected with miR-199a-3p lentiviral vector or TLR4 antagonist (TAK-242). Next, cardiac function of rats was examined by echocardiography, and rat serum indicators, oxidative stress levels and inflammatory factors were detected. HE staining was applied to detect pathological tissue structure, TUNEL staining to detect apoptosis rate, qRCR and western blot to detect miR-199a-3p and TLR4/MyD88/NF-κB expressions in rat myocardial tissues. Dual luciferase reporter experiment was conducted to confirm the relationship between miR-199a-3p and TLR4. In conclusion, PHC suppresses TLR4/MyD88/NF-κB signalling pathway through miR-199a-3p, thereby improving MI/RI in rats.

盐酸戊乙奎醚通过miR-199a-3p抑制TLR4/MyD88/NF-κB通路对大鼠心肌缺血再灌注损伤的影响
本研究旨在通过miR-199a-3p探讨盐酸戊乙基乙胺(PHC)介导toll样受体4 (TLR4)/髓样分化因子88 (MyD88)/核因子κB (NF-κB)信号通路对大鼠心肌缺血再灌注损伤(MI/RI)的影响。结扎冠状动脉左前降支(LAD)建立大鼠心肌梗死/心肌梗死模型。模型大鼠术前注射PHC,并注射miR-199a-3p慢病毒载体或TLR4拮抗剂(TAK-242)。然后用超声心动图检测大鼠心功能,检测大鼠血清指标、氧化应激水平和炎症因子。采用HE染色检测病理组织结构,TUNEL染色检测细胞凋亡率,qRCR和western blot检测大鼠心肌组织中miR-199a-3p和TLR4/MyD88/NF-κB的表达。双荧光素酶报告基因实验证实miR-199a-3p与TLR4之间的关系。综上所述,PHC通过miR-199a-3p抑制TLR4/MyD88/NF-κB信号通路,从而改善大鼠MI/RI。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Growth factors
Growth factors 生物-内分泌学与代谢
CiteScore
2.60
自引率
0.00%
发文量
20
审稿时长
>12 weeks
期刊介绍: Growth Factors is an international and interdisciplinary vehicle publishing new knowledge and findings on the regulators of cell proliferation, differentiation and survival. The Journal will publish research papers, short communications and reviews on current developments in cell biology, biochemistry, physiology or pharmacology of growth factors, cytokines or hormones which improve our understanding of biology or medicine. Among the various fields of study topics of particular interest include: •Stem cell biology •Growth factor physiology •Structure-activity relationships •Drug development studies •Clinical applications
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