首页|宽胸气雾剂通过调控TLR4/MyD88/NLRP3/Caspase-1通路减轻心梗诱导的大鼠心肌细胞损伤

宽胸气雾剂通过调控TLR4/MyD88/NLRP3/Caspase-1通路减轻心梗诱导的大鼠心肌细胞损伤

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[目的]探索宽胸气雾剂(Kuanxiong aerosol,KXA)对异丙肾上腺素(isoproterenol,ISO)诱导的心肌梗死(myocardial infarction,MI)大鼠心肌炎症和细胞焦亡的影响,并分析其对焦亡关键通路Toll样受体4(Toll-like receptor 4,TLR4)/髓样分化因子(myeloid differentiation primary response gene 88,MyD88)/NOD 样受体热蛋白结构域相关蛋白 3(NOD-like receptor pyrin domain containing 3,NLRP3)/胱天蛋白酶-1(cysteinyl aspartate specific proteinase-1,caspase-1)的作用.[方法]按体质量将 30 只雄性 Wistar 大鼠随机分为5组:对照组(0.9%氯化钠溶液)、模型组(ISO 120 mg·kg-1)、单硝酸异山梨酯组(ISO 120 mg·kg-1+单硝酸异山梨酯5 mg/kg·d)、KXA低剂量组(ISO 120 mg·kg-1+KXA 0.1 mL/kg·d)和 KXA 高剂量组(ISO 120 mg·kg-1+KXA 0.3 mL/kg·d),每组6 只,连续灌胃14 d,并在第13、14天腹腔注射ISO.末次干预结束后,麻醉采血、分离心脏,以酶联免疫吸附试验(enzyme-linked immunosorbent assay,ELISA)检测各组血清肌酸激酶同工酶(creatine kinase-MB,CK-MB)和心肌肌钙蛋白T(cardiac troponin T,cTnT)水平,以及血清白细胞介素-6(interleukin-6,IL-6)、白细胞介素-18(interleukin-18,IL-18)、白细胞介素-1 β(interleukin-1 β,IL-1 β)和肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)水平;苏木精-伊红(hematoxylin-eosin,HE)染色检测心肌病理变化;转录组测序分析各组心肌基因表达差异;免疫印迹检测焦亡通路相关蛋白的表达情况.[结果]与对照组比较,模型组cTnT和CK-MB检测显著升高,差异具有统计学意义(P<0.01),表明MI大鼠模型构建成功.HE染色显示,KXA和单硝酸异山梨酯干预后心肌纤维排列断裂、紊乱情况明显减轻.转录组测序显示,对照组和模型组之间存在2 646个差异基因;模型组和KXA组之间存在714个差异基因,进一步分析发现130个基因表达上调,7个基因表达下调,其中炎症相关性通路TLR4通路被显著富集.与模型组比较,KXA高剂量组、KXA低剂量组和单硝酸异山梨酯组血清IL-6、IL-18、IL-1β和TNF-α表达显著减少,差异具有统计学意义(P<0.01,P<0.05).免疫印迹显示,模型组TLR4、MyD88、磷酸化核因子-κB p65(phospho-nuclear factor-κB,p-NF-κB)p65、NLRP3、切割的胱天蛋白酶-1(cleaved caspase-1)和消皮素D蛋白N端结构域(Gasdermin D-N,GSDMD-N)表达显著高于对照组;而KXA高剂量组、KXA低剂量组和单硝酸异山梨酯组的表达显著低于模型组(P<0.05,P<0.01).[结论]KXA可以改善心肌缺血,减轻心脏损伤,抑制心肌细胞焦亡和炎症反应,其机制可能与调节TLR4/MyD88/NLRP3/caspase-1信号通路有关.
Kuanxiong Aerosol Regulates TLR4/MyD88/NLRP3/Caspase-1 Pathway to Reduce Cardiomyocyte Injury in Myocardial Infarc-tion Rats
[Objective]To investigate the effects of Kuanxiong aerosol(KXA)on pyroptosis and inflammatory response in isoproterenol(ISO)-induced myocardial infarction(MI)rats,and its effect on the key pathway of pyroptosis Toll-like receptor 4(TLR4)/myeloid differentiation primary response gene 88(MyD88)/NOD-like receptor pyrin domain containing 3(NLRP3)/cysteinyl aspartate specific proteinase-1(caspase-1).[Methods]Thirty male Wistar rats were randomly divided into five groups,6 rats in each group,as control group(0.9%sodium chloride solution),model group(ISO 120 mg·kg-1),isosorbide mononitrate(IMSN)group(ISO 120 mg·kg-1+IMSN 5 mg/kg·d),KXA low dose group(ISO 120 mg·kg-1+KXA 0.1 mL/kg·d),and KXA high dose group(ISO 120 mg·kg-1+KXA 0.3 mL/kg·d),gave continuous intragastric administration for 14 days,and intraperitoneal injection of ISO on the 13th and 14th day.After the last intervention,collected heart tissues and blood under anesthesia.Enzyme-linked immunosorbent assay(ELISA)was performed to investigate the expression of creatine kinase-MB(CK-MB)and cardiac troponin T(cTnT),as well as serum inflammatory indicators such as interleukin-1β(IL-1β),interleukin-18(IL-18),interleukin-6(IL-6)and tumor necrosis factor-α(TNF-α).The histopathological changes in heart tissue were evaluated using hematoxylin-eosin(HE)staining,and RNA-sequencing was used to detect the differential expression genes among groups.And the expression of the pyroptosis relevant protein was detected by Western blot.[Results]The results of the ELISA showed that CK-MB and cTnT expression in model group were significantly higher than those in control group(P<0.01),which meant successful model construction.Pathological staining results showed disordered and fractured muscle fibers were significantly improved after KXA and IMSN intervention.RNA-seq results showed there were 2 646 different genes between model group and control group,while 714 other genes were in KXA and model group.After analyzing these two compared groups,it found that there were 130 up-regulated genes and 7 down-regulated genes;among them,inflammation related TLR4 pathway was significantly enriched.Furthermore,compared with model group,the expression of inflammatory factors IL-1β,IL-18,IL-6 and TNF-α decreased significantly in KXA groups and IMSN group(P<0.01,P<0.05),and Western blot showed that the protein expression of TLR4,MyD88,phospho-nuclear factor-KB(p-NF-KB)p65,NLRP3,cleaved cysteinyl aspartate specific proteinase-1(cleaved caspase-1)and Gasdermin D-N(GSDMD-N)increased significantly in model group while significantly down-regulated in KXA groups and IMSN group(P<0.05,P<0.01).[Conclusion]KXA can improve myocardial ischemia,reduce cardiac damage,and inhibit cardiomyocyte pyroptosis and inflammatory response,the mechanism may be related to regulating the TLR4/MyD88/NLRP3/caspase-1 signaling pathway.

Kuanxiong aerosolmyocardial infarctionpyroptosisinflammationTLR4NLRP3

王乙连、何晨晨、张珊苑、韦琛谊、褚剑锋

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福建中医药大学中西医研究院 福州 350122

福建省中西医结合老年性疾病重点实验室

福建中医药大学陈可冀学术思想传承工作室

宽胸气雾剂 心肌梗死 焦亡 炎症 TLR4 NLRP3

福建省科技计划

2021L3014

2024

浙江中医药大学学报
浙江中医药大学

浙江中医药大学学报

CSTPCD
影响因子:1.049
ISSN:1005-5509
年,卷(期):2024.48(1)
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