首页|达格列净调控JAK2/STAT3轴对大鼠缺血性室性心律失常的作用

达格列净调控JAK2/STAT3轴对大鼠缺血性室性心律失常的作用

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目的 探讨达格列净(DAPA)调控蛋白酪氨酸激酶2(JAK2)/信号转导子与激活子3(STAT3)轴对大鼠缺血性室性心律失常(VA)的作用及机制研究.方法 将大鼠随机分为假手术组、模型组和低、中、高剂量实验组及AG490组,每组10只.除假手术组外各组用结扎冠状动脉左前降支(LAD)构建大鼠缺血性VA模型.造模后48 h,低、中、高剂量实验组分别给予大鼠1、3、5 mg·kg-1 DAPA 灌胃,AG490 组灌胃 5 mg·kg-1 DAPA+5 mg·kg1 AG490,每日 1 次,持续30 d.用心电图检查大鼠心律失常评分,用蛋白质印迹法检测心肌组织中磷酸化 JAK2(p-JAK2)/JAK2 和磷酸化 STAT3(p-STAT3)/STAT3 蛋白的表达水平.结果 假手术组、模型组、低、中、高剂量实验组和AG490组的心律失常评分分别为(0.00±0.00)、(4.36±0.52)、(3.41±0.42)、(2.84±0.33)、(2.13±0.26)和(3.74±0.43)分,p-JAK2/JAK2相对表达水平比值分别为0.98±0.10、0.41±0.05、0.62±0.07、0.74±0.08、0.91±0.09 和 0.52±0.06,p-STAT3/STAT3相对表达水平比值分别为0.93±0.09、0.33±0.04、0.57±0.06、0.78±0.08、0.89±0.09 和 0.49±0.05.模型组的上述指标与假手术组、低、中、高剂量实验组比较,AG490组的上述指标与高剂量实验组比较,在统计学上差异均有统计学意义(均P<0.05).结论 DAPA可能通过激活JAK2/STAT3信号通路,抑制炎症反应和氧化应激,改善大鼠缺血性VA.
Effects of dapagliflozin on ischemic ventricular arrhythmia in rats by regulating JAK2/STAT3 axis
Objective To investigate the effect and mechanism of dapagliflozin(DAPA)on ischemic ventricular arrhythmia(VA)in rats by regulating the Janus kinase 2(JAK2)/signal transducer and activator of transcription 3(STAT3)axis.Methods The rats were randomly divided into sham operation group,model group,experimental-L,-M,-H groups and AG490 group.All groups except sham group were established model of ischemic VA by ligation of the left anterior descending coronary artery(LAD).After 48 h of modeling,the experimental-L,-M,-H groups were given 1,3,5 mg·kg-1 DAPA by gavage,respectively;the AG490 group were given 5 mg·kg-1 DAPA+5 mg·kg-1 AG490 by gavage,once a day for 30 days.The arrhythmia scores of rats were examined by electrocardiogram;the expression levels of phosphorylated JAK2(p-JAK2)/JAK2 and phosphorylated STAT3(p-STAT3)/STAT3 proteins in myocardial tissue were detected by Western blotting.Results The arrhythmia scores of the sham operation group,model group,experimental-L,-M,-H groups and AG490 group were(0.00±0.00),(4.36±0.52),(3.41±0.42),(2.84±0.33),(2.13±0.26)and(3.74±0.43)points;the relative expression levels of p-JAK2/JAK2 were 0.98±0.10,0.41±0.05,0.62±0.07,0.74±0.08,0.91±0.09 and 0.52±0.06;the relative expression levels of p-STAT3/STAT3 were 0.93±0.09,0.33±0.04,0.57±0.06,0.78±0.08,0.89±0.09 and 0.49±0.05,respectively.There were significant differences in the above indexes between the model group and the sham operation group,experimental-L,-M,-H groups(all P<0.05);compared with the experimental-H group,the difference of AG490 was statistically significant(all P<0.05).Conclusion DAPA may improve ischemic VA in rats by activating the JAK2/STAT3 signaling pathway and inhibiting inflammatory response and oxidative stress.

ischemic ventricular arrhythmiadapagliflozinJanus kinase 2/signal transducer and activator of transcription 3

凌静、吴瑶、田国平

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南华大学附属第二医院功能检查科,湖南衡阳 421001

南华大学附属第二医院心血管内科,湖南衡阳 421001

缺血性室性心律失常 达格列净 蛋白酪氨酸激酶2/信号转导子与激活子3

湖南省自然科学基金资助项目

2021JJ30608

2024

中国临床药理学杂志
中国药学会

中国临床药理学杂志

CSTPCD北大核心
影响因子:1.91
ISSN:1001-6821
年,卷(期):2024.40(3)
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